{"title":"ANALYSIS","description":null,"products":[{"product_id":"contenitore-urine-alvita-prontotest-24ore","title":"ALVITA PRONTOTEST 24-HOUR URINE CONTAINER","description":"\u003ch1\u003eProntotest\u003c\/h1\u003e \u003cb\u003e24-HOUR URINE CONTAINER\u003c\/b\u003e\u003cbr\u003e \u003cbr\u003e \u003cb\u003eIndications:\u003c\/b\u003e\u003cbr\u003e in vitro diagnostic medical device, suitable for containing urine for laboratory analysis.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFeatures:\u003c\/b\u003e\u003cbr\u003e polyethylene container, single-use, hygienic.\u003cbr\u003e 2500 ml graduated bottle, with a polypropylene screw cap and a cap for sample collection.\u003cbr\u003e Boxed in a single package, complete with a self-adhesive label for sample identification.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eWarnings:\u003c\/b\u003e\u003cbr\u003e product validity: 5 years.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCode\u003c\/b\u003e AVTA187792","brand":"ALLIANCE HEALTHCARE IT.DIS.SpA","offers":[{"title":"Default Title","offer_id":45579219894539,"sku":"904578515","price":3.22,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_5bb4f254-85b6-482a-ab85-c791af6dce96.jpg?v=1720001084"},{"product_id":"contenitore-urine-alvita-prontotest-tappo-a-vite","title":"ALVITA PRONTOTEST URINE CONTAINER SCREW CAP","description":"\u003ch1\u003eProntotest\u003c\/h1\u003e \u003cb\u003eURINE CONTAINER\u003c\/b\u003e\u003cbr\u003e \u003cbr\u003e \u003cb\u003eIndications:\u003c\/b\u003e\u003cbr\u003e In vitro diagnostic medical device, suitable for containing biological fluids for laboratory analysis.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFeatures:\u003c\/b\u003e\u003cbr\u003e Sterile 150 ml urine container made of transparent, non-toxic, hygienic, graduated polypropylene, with a screw cap made of polyethylene that ensures perfect sealing during transport.\u003cbr\u003e Individually boxed, complete with self-adhesive label for sample identification.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCode\u003c\/b\u003e AVTA187790","brand":"ALLIANCE HEALTHCARE IT.DIS.SpA","offers":[{"title":"Default Title","offer_id":45579220222219,"sku":"904578491","price":1.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_b1818061-aca0-47cb-bbb6-89af06f5c551.jpg?v=1720001091"},{"product_id":"contenitore-alvita-prontotest-feci","title":"ALVITA PRONTOTEST STOOL CONTAINER","description":"\u003ch1\u003eProntotest\u003c\/h1\u003e \u003cb\u003eSTOOL CONTAINER\u003c\/b\u003e\u003cbr\u003e \u003cbr\u003e \u003cb\u003eIndications:\u003c\/b\u003e\u003cbr\u003e in vitro diagnostic medical device suitable for containing biological samples for laboratory analysis.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFeatures:\u003c\/b\u003e\u003cbr\u003e 60 ml sterile, transparent polypropylene container.\u003cbr\u003e Non-toxic.\u003cbr\u003e Gamma-ray sterilized with irradiation not less than 2.5 MRAD.\u003cbr\u003e Non-graduated, with screw cap in polyethylene and spatula that ensures perfect sealing during transport.\u003cbr\u003e Boxed in a single package, complete with self-adhesive label for sample identification.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCode.\u003c\/b\u003e AVTA187789","brand":"ALLIANCE HEALTHCARE IT.DIS.SpA","offers":[{"title":"Default Title","offer_id":45579220353291,"sku":"904578489","price":0.26,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_ff13af51-7269-47af-8be4-0c3c464f09bb.jpg?v=1720001099"},{"product_id":"silvercross-contenitore-urina-120ml","title":"SILVERCROSS URINE CONTAINER 120ML","description":"\u003cfont size=\"6\"\u003eSANITARY\u003c\/font\u003e\u003cbr\u003e \u003cbr\u003e \u003cfont size=\"6\"\u003e\u003cb\u003eSILVER\u003cbr\u003e CROSS\u003c\/b\u003e\u003c\/font\u003e\u003cbr\u003e \u003cbr\u003e \u003cfont size=\"4\"\u003e\u003cb\u003eSTERILE\u003cbr\u003e CONTAINER\u003c\/b\u003e\u003cbr\u003e FOR URINE\u003c\/font\u003e\u003cbr\u003e \u003cbr\u003e Indicated for the collection and transport of urine samples. The container is designed for identification via a dedicated writable area. Product sterilized with beta rays.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Container with a capacity of 120 ml\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCode\u003c\/b\u003e SAN00020","brand":"COMIFAR DISTRIBUZIONE SpA","offers":[{"title":"Default Title","offer_id":45700169662731,"sku":"922377546","price":1.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_04cf2adb-cfca-483f-8f5f-805f204ee88d.jpg?v=1722358239"},{"product_id":"test-antigenico-rapido-covid-19-flowflex-autodiagnostico-determinazione-qualitativa-antigeni-sars-cov-2-in-tamponi-nasali-mediante-immunocromatografia-provetta-con-alluminio","title":"COVID-19 FLOWFLEX RAPID ANTIGEN TEST SELF-TEST QUALITATIVE DETECTION OF SARS-COV-2 ANTIGENS IN NASAL SWABS BY IMMUNOCHROMATOGRAPHY ALUMINUM FOIL POUCH","description":"\u003ch1\u003eFlowflex\u003c\/h1\u003e \u003ch2\u003eSARS-CoV-2 Antigen Rapid Test\u003cbr\u003e (Self-Testing)\u003c\/h2\u003e \u003cdiv align=\"justify\"\u003e \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e A lateral flow test for the qualitative detection of SARS-CoV-2 nucleocapsid antigen in anterior nasal swab samples taken directly from individuals suspected of COVID-19 within the first 7 days of symptom onset.\u003cbr\u003e The test can be used to analyze samples from asymptomatic subjects.\u003cbr\u003e It does not distinguish between SARS-CoV and SARS-CoV-2.\u003cbr\u003e The results relate to the identification of SARS-CoV-2 antigen. This antigen is generally found in samples taken from the upper respiratory tract during the acute phase of infection.\u003cbr\u003e Positive results indicate the presence of viral antigens, but patient history and other personal diagnostic data are necessary to determine the infection status. Positive results do not rule out bacterial infections or simultaneous infection with other viruses. The detected pathogen may not be the exact cause of the illness.\u003cbr\u003e Negative results obtained from subjects with symptoms that appeared more than seven days ago should be treated as probable negatives. If necessary, seek confirmation through molecular analysis.\u003cbr\u003e Negative results do not rule out SARS-CoV-2 infection.\u003cbr\u003e Test results are read visually within 15-30 minutes, based on the presence or absence of colored lines.\u003cbr\u003e A colored line with a procedural control function will always appear in the control line area, indicating that a sufficient sample volume has been inserted and that membrane absorption has occurred.\u003cbr\u003e The test is intended for use as an aid in the diagnosis of SARS-CoV-2 infection.\u003cbr\u003e The usability of self-tests performed by individuals under 18 years of age has not been determined. It is recommended that individuals under 18 years of age be tested by an adult.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eInstructions for use\u003c\/b\u003e\u003cbr\u003e \u003cu\u003ePreparation\u003c\/u\u003e\u003cbr\u003e Wash or disinfect hands. Ensure they are dry before starting the test. Read the instructions carefully before performing the test.\u003cbr\u003e Check the expiry date printed on the foil pouch. Open the pouch and check the result window and the sample well on the cassette.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eSample collection\u003c\/u\u003e\u003cbr\u003e Sample collection can be done by oneself or by a caregiver.\u003cbr\u003e Self-collection of the sample can be performed by individuals aged 18 or over.\u003cbr\u003e Children under 18 years of age must be tested by a parent or legal guardian. Follow local guidelines for collecting samples from children.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eProcedure\u003c\/u\u003e\u003cbr\u003e Unscrew the dropper cap from the extraction solution tube without squeezing it. Insert the tube into the hole on the kit box (or place the tube in the tube holder). Open the swab packaging at the stick end.\u003cbr\u003e Caution: do not touch the absorbent tip of the swab with your hands.\u003cbr\u003e Insert the entire absorbent tip of the swab into one nostril. Using a gentle rotation, push the swab less than 2.5 cm from the edge of the nostril. Rotate the swab five times, gently touching the inside of the nostril. Remove the swab and insert it into the other nostril, repeating the step. Remove the swab from the nostril and insert it into the tube, moving it in a circular motion for 30 seconds. Rotate the swab 5 times, while compressing the side of the tube. Remove the swab while compressing the tube.\u003cbr\u003e Securely attach the dropper tip to the extraction buffer tube containing the sample. Mix thoroughly by rotating or flicking the bottom of the tube. Unscrew the small cap from the end of the dropper. Gently squeeze the tube and dispense 4 drops of solution into the sample well.\u003cbr\u003e Read the result when the timer reaches 15-30 minutes. Do not read after 30 minutes.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eInterpretation of results\u003c\/u\u003e\u003cbr\u003e - NEGATIVE: only the control line (C) appears and no test line (T). This means that no SARS-CoV-2 antigen has been detected. A negative test result indicates that you are unlikely to have COVID-19 at this time. Continue to comply with all current rules and protective measures when in contact with other people. It is possible that an infection is present even if the test is negative. If suspected, repeat the test after 1-2 days, as the coronavirus cannot be accurately detected in all phases of the infection.\u003cbr\u003e \u003cbr\u003e - POSITIVE: both the control line (C) and the test line (T) appear. This means that SARS-CoV-2 antigen has been detected. A positive test result indicates a very high probability of active COVID-19 infection. Contact your doctor\/general practitioner or local health authority immediately. Follow local guidelines for self-isolation. A confirmatory PCR test must be performed.\u003cbr\u003e Note: any line, even a very faint one, present in the test line area (T) should be considered positive.\u003cbr\u003e \u003cbr\u003e - INVALID: the control line (C) does not appear. The most likely reasons for an invalid result are insufficient sample volume or incorrect procedure. Re-read the instructions and repeat the test with a new cassette. If test results continue to be invalid, contact your doctor or a COVID-19 testing center.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e Before performing the test, carefully read the leaflet in the test package. Failure to follow the instructions may lead to inaccurate test results.\u003cbr\u003e Do not use the test after the expiry date indicated on the pouch.\u003cbr\u003e Do not eat, drink, or smoke before and during the test.\u003cbr\u003e Do not use the test if the pouch is damaged.\u003cbr\u003e All used tests, samples, and potentially contaminated material must be disposed of according to local regulations.\u003cbr\u003e Humidity and temperature can negatively affect results.\u003cbr\u003e The test line for a sample with a high viral load may appear within 15 minutes or even earlier, when the sample passes the test line area.\u003cbr\u003e The test line for a sample with a low viral load may appear within 30 minutes.\u003cbr\u003e Do not collect the nasal swab sample if you have a nosebleed.\u003cbr\u003e Wash hands thoroughly after use.\u003cbr\u003e If the extraction swab accidentally comes into contact with skin or eyes, rinse with large amounts of water and consult a doctor if necessary.\u003cbr\u003e The SARS-CoV-2 Antigen Rapid Test is for self-testing only. The test should only be used for the detection of nucleocapsid antigen from SARS-CoV-2 in anterior nasal swab samples. The intensity of the test line is not necessarily correlated with the SARS-CoV-2 viral load in the sample.\u003cbr\u003e A false negative test may be obtained if the antigen concentration in a sample is below the detection limit of the test or if the sample was collected incorrectly.\u003cbr\u003e Test results should be considered in light of other clinical data available to the physician.\u003cbr\u003e Positive results do not rule out the presence of co-infections caused by other pathogens. Positive results do not distinguish between SARS-CoV and SARS-CoV-2.\u003cbr\u003e Negative test results do not rule out the presence of other viral or bacterial infections.\u003cbr\u003e A negative result obtained from a subject with symptoms that appeared more than seven days ago should be treated as a probable negative and, if necessary, verified by molecular analysis.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eStorage\u003c\/b\u003e\u003cbr\u003e Store the kit at a temperature between 2°C and 30°C. Do not freeze.\u003cbr\u003e The test must remain in the sealed pouch until use.\u003cbr\u003e The test is stable until the expiry date printed on the sealed pouch. Do not use after the expiry date.\u003cbr\u003e Shelf life unopened: 24 months.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e The kit contains:\u003cbr\u003e - test cassette;\u003cbr\u003e - extraction buffer tube;\u003cbr\u003e - disposable swab;\u003cbr\u003e - waste bag;\u003cbr\u003e - instructions for use.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eBibliography\u003c\/b\u003e\u003cbr\u003e 1. Shuo Su, Gary Wong, Weifeng Shi, et al. Epidemiology, Genetic recombination and pathogenesis of coronaviruses. Trends in Microbiology, June 2016, vol. 24, No. 6: 409-502\u003cbr\u003e 2. Susan R.Weiss, Julian L. Leibowitz, Coronavirus Pathogenesis, Advances in Virus Research, Volume 81: 85-164\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCode\u003c\/b\u003e L031-11855\u003c\/div\u003e","brand":"PM2 SERVICES Srl","offers":[{"title":"Default Title","offer_id":45773949698315,"sku":"982653709","price":3.9,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_cf3e6d1c-3a2a-4d8a-b925-c568a2870239.jpg?v=1724216560"},{"product_id":"alvita-prontotest-contenitore-urine-provetta-10-ml","title":"ALVITA PRONTOTEST URINE CONTAINER 10 ML TUBE","description":"\u003ch1\u003eProntotest\u003c\/h1\u003e \u003cb\u003eURINE TUBE\u003c\/b\u003e\u003cbr\u003e \u003cbr\u003e \u003cb\u003eIndications:\u003c\/b\u003e\u003cbr\u003e In vitro diagnostic medical device, suitable for containing urine for laboratory analysis.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCharacteristics:\u003c\/b\u003e\u003cbr\u003e Sterile transparent polystyrene tube, 12 ml, with polyethylene cap.\u003cbr\u003e With wide mouth, graduated, with snap cap.\u003cbr\u003e Packaged in a single box and supplied with a label for sample identification.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCode:\u003c\/b\u003e AVTA187791","brand":"ALLIANCE HEALTHCARE IT.DIS.SpA","offers":[{"title":"Default Title","offer_id":45799417905419,"sku":"904578503","price":0.19,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_d2ba53af-16e5-4a5d-bd19-cf3d337759fc.jpg?v=1724836365"},{"product_id":"strisce-misurazione-glicosuria-e-chetonuria-ketodiastix-50-pezzi","title":"KETODIASTIX GLUCOSURIA AND KETONURIA MEASURING STRIPS 50 PIECES","description":"\u003ch1\u003eKeto-Diastix\u003c\/h1\u003e \u003cb\u003eREAGENT STRIPS\u003c\/b\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eIndications:\u003c\/b\u003e\u003cbr\u003e Test for the simultaneous semi-quantitative determination of glucose and ketone bodies in urine.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCode\u003c\/b\u003e 2883C","brand":"ASCENSIA DIABETES CARE ITALY","offers":[{"title":"Default Title","offer_id":45799460929803,"sku":"908575451","price":11.5,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_46d6aa8c-98a5-4d8c-9c96-c2ea5ba48fdc.jpg?v=1724837605"},{"product_id":"strisce-misurazione-chetonuria-ketostix-50-pezzi","title":"KETOSTIX KETONURIA MEASURING STRIPS 50 PIECES","description":"\u003ch1\u003eKetostix\u003c\/h1\u003e \u003cb\u003eREAGENT STRIPS\u003c\/b\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFeatures:\u003c\/b\u003e\u003cbr\u003e Test for the semi-quantitative determination of ketone bodies in urine.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCode\u003c\/b\u003e 2880C","brand":"ASCENSIA DIABETES CARE ITALY","offers":[{"title":"Default Title","offer_id":45799460995339,"sku":"908575855","price":6.45,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_f977d8f8-e87c-4884-a869-694b3cff8b0e.jpg?v=1724837614"},{"product_id":"test-perdite-liquido-amniotico-amnios-assorbente-2-pezzi","title":"AMNIOTIC FLUID LEAK TEST AMNIOS ABSORBENT 2 PIECES","description":"\u003ch1\u003eAMNIOS\u003c\/h1\u003e \u003ch3\u003eABSORBENT TEST 2PCS\u003c\/h3\u003eHome-based test for the detection of amniotic fluid leakage. \u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e 2 pieces.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCode.\u003c\/b\u003ePL02A","brand":"IDI INTEGRATORI DIETET.IT. Srl","offers":[{"title":"Default Title","offer_id":45799536722187,"sku":"923005995","price":14.09,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_47bc751e-a3b8-4285-9351-42a7182c35d7.jpg?v=1724839546"},{"product_id":"contenitore-urina-baby-femmina","title":"URINE SPECIMEN COLLECTOR FOR INFANT GIRLS","description":"\u003ch1\u003e FEMALE BABY URINE COLLECTOR \u003c\/h1\u003e","brand":"GAMMADIS FARMACEUTICI Srl","offers":[{"title":"Default Title","offer_id":45799615627531,"sku":"926647595","price":0.81,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_811505ef-c7e6-4f6d-9ab4-8c59535708af.jpg?v=1724840720"},{"product_id":"contenitore-urina-baby-maschio","title":"MALE BABY URINE COLLECTOR","description":"\u003ch1\u003eMALE BABY URINE COLLECTOR\u003c\/h1\u003e","brand":"GAMMADIS FARMACEUTICI Srl","offers":[{"title":"Default Title","offer_id":45799615725835,"sku":"926647607","price":0.81,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_e08dc021-641f-4024-ad07-7d30a838dc2b.jpg?v=1724840728"},{"product_id":"strisce-misurazione-glicemia-glucomen-areo-sensor-25-pezzi","title":"GLUCOMEN AREO SENSOR BLOOD GLUCOSE TEST STRIPS 25 COUNT","description":"\u003ch1\u003eGlucoMen\u003cbr\u003e areo \u003ci\u003eSensor\u003c\/i\u003e\n\u003c\/h1\u003e \u003cdiv align=\"justify\"\u003e\n\u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eIn vitro\u003c\/i\u003e diagnostic medical device.\u003cbr\u003e Sensors for the quantitative determination of glucose levels in fresh capillary whole blood; for exclusive use with the GlucoMen areo 2K device.\u003cbr\u003e The sensors are designed for monitoring and self-monitoring of blood glucose levels in people with diabetes mellitus; they can also be used in hospitals by medical and healthcare personnel.\u003cbr\u003e Not intended for use in the diagnosis or screening of diabetes or for use in neonates.\u003cbr\u003e Do not change your treatment based on test results without first consulting your doctor or healthcare personnel.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eGeneral characteristics\u003c\/b\u003e\u003cbr\u003e \u003ctable border=\"1cellspacing=0cellpadding=1\" width=\"500\"\u003e \u003ctr\u003e\n\u003ctd\u003e\u003cb\u003eBlood glucose measurement\u003c\/b\u003e\u003c\/td\u003e\n\u003ctd align=\"center\"\u003especificity for beta-D-glucose in blood\u003c\/td\u003e\n\u003c\/tr\u003e \u003ctr\u003e\n\u003ctd\u003e\u003cb\u003eEnzymatic composition (per cm\u003csup\u003e2\u003c\/sup\u003e) of a test strip for blood glucose measurement\u003c\/b\u003e\u003c\/td\u003e\n\u003ctd align=\"Center\"\u003e- glucose oxidase (from \u003ci\u003eAspergillus niger\u003c\/i\u003e), 3.5%\u003cbr\u003e - mediator: hexacyanoferrate (III) ion, 17.5%\u003cbr\u003e - non-reactive substances, 79%\u003c\/td\u003e\n\u003c\/tr\u003e \u003ctr\u003e\u003ctd colspan=\"2\"\u003e\u003cb\u003eUnit of measurement\u003c\/b\u003e\u003c\/td\u003e\u003c\/tr\u003e \u003ctr\u003e\n\u003ctd\u003eGlucose\u003c\/td\u003e\n\u003ctd align=\"Center\"\u003emg\/dL (not modifiable)\u003c\/td\u003e\n\u003c\/tr\u003e \u003ctr\u003e\u003ctd colspan=\"2\"\u003e\u003cb\u003eMeasurement range\u003c\/b\u003e\u003c\/td\u003e\u003c\/tr\u003e \u003ctr\u003e\n\u003ctd\u003eGlucose\u003c\/td\u003e\n\u003ctd align=\"Center\"\u003e20-600 mg\/dL\u003c\/td\u003e\n\u003c\/tr\u003e \u003ctr\u003e\u003ctd colspan=\"2\"\u003e\u003cb\u003eResponse time\u003c\/b\u003e\u003c\/td\u003e\u003c\/tr\u003e \u003ctr\u003e\n\u003ctd\u003eGlucose\u003c\/td\u003e\n\u003ctd align=\"Center\"\u003e5 seconds\u003c\/td\u003e\n\u003c\/tr\u003e \u003ctr\u003e\u003ctd colspan=\"2\"\u003e\u003cb\u003eSample volume\u003c\/b\u003e\u003c\/td\u003e\u003c\/tr\u003e \u003ctr\u003e\n\u003ctd\u003eGlucose\u003c\/td\u003e\n\u003ctd align=\"Center\"\u003e0.5 microL\u003c\/td\u003e\n\u003c\/tr\u003e \u003ctr\u003e\u003ctd colspan=\"2\"\u003e\u003cb\u003eHematocrit acceptability range\u003c\/b\u003e\u003c\/td\u003e\u003c\/tr\u003e \u003ctr\u003e\n\u003ctd\u003eGlucose\u003c\/td\u003e\n\u003ctd align=\"Center\"\u003eautomatically corrects the measurement based on hematocrit (10-70%)\u003c\/td\u003e\n\u003c\/tr\u003e \u003ctr\u003e\n\u003ctd\u003e\u003cb\u003eCorrelation\u003c\/b\u003e\u003c\/td\u003e\n\u003ctd align=\"Center\"\u003eplasma equivalent\u003c\/td\u003e\n\u003c\/tr\u003e \u003ctr\u003e\n\u003ctd\u003e\u003cb\u003eSample\u003c\/b\u003e\u003c\/td\u003e\n\u003ctd align=\"Center\"\u003efresh capillary whole blood\u003c\/td\u003e\n\u003c\/tr\u003e \u003ctr\u003e\n\u003ctd\u003e\u003cb\u003eSensor coding\u003c\/b\u003e\u003c\/td\u003e\n\u003ctd align=\"Center\"\u003eauto-coding\u003c\/td\u003e\n\u003c\/tr\u003e \u003ctr\u003e\n\u003ctd\u003e\u003cb\u003eHygiene\u003c\/b\u003e\u003c\/td\u003e\n\u003ctd align=\"Center\"\u003eautomatic test strip ejection using a dedicated ejection button\u003c\/td\u003e\n\u003c\/tr\u003e \u003ctr\u003e\n\u003ctd\u003e\u003cb\u003eSampling\u003c\/b\u003e\u003c\/td\u003e\n\u003ctd align=\"Center\"\u003eautomatic blood sample aspiration by capillarity\u003c\/td\u003e\n\u003c\/tr\u003e \u003ctr\u003e\n\u003ctd\u003e\u003cb\u003eUse of alternative sites (AST)\u003c\/b\u003e\u003c\/td\u003e\n\u003ctd align=\"Center\"\u003eallowed (palm and forearm)\u003c\/td\u003e\n\u003c\/tr\u003e \u003ctr\u003e\n\u003ctd\u003e\u003cb\u003eOperating environment\u003c\/b\u003e\u003c\/td\u003e\n\u003ctd align=\"Center\"\u003etemperature range: 5-45°C\u003cbr\u003e humidity: 20%-90% (non-condensing)\u003c\/td\u003e\n\u003c\/tr\u003e \u003c\/table\u003e \u003cbr\u003e \u003cb\u003eHow to use\u003c\/b\u003e\u003cbr\u003e 1. Insert a new GlucoMen areo Sensor (white color) into the sensor insertion slot. The drop symbol will start flashing on the display and the Glu glucose symbol will appear at the bottom left. If nothing appears on the display, remove the sensor, reinsert it into the slot and wait for the drop symbol to start flashing.\u003cbr\u003e For information on how to use the lancing device, read the relevant instructions for use.\u003cbr\u003e 2. Hold the end of the sensor in contact with the blood drop until the control window is filled. A beep will then sound (if enabled) and the display will show a countdown.\u003cbr\u003e 3. Read the test results. A beep will announce the appearance of the test result on the screen with the Glu glucose symbol.\u003cbr\u003e 4. To remove the sensor, press the eject button. The device will turn off.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e Keep the device, sensors and other components out of reach and sight of children. Small parts can be a choking hazard.\u003cbr\u003e Handle the vial and sensors with clean, dry hands.\u003cbr\u003e Dispose of the vial and used sensors in accordance with local regulations.\u003cbr\u003e Handling blood can be dangerous: exercise extreme caution when handling blood, sensors, lancets and the device.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eStorage\u003c\/b\u003e\u003cbr\u003e Store the sensor vial in a dry place, at a temperature of 4-30°C. Do not freeze. Avoid heat and direct sunlight.\u003cbr\u003e Store all unused sensors in the original vial and after removing one, close the cap tightly to preserve its quality. Do not transfer sensors to other containers.\u003cbr\u003e Do not use sensors beyond their expiration date.\u003cbr\u003e Do not use sensors more than 12 months after first opening their vial. It is recommended to write the disposal date (first opening date + 12 months) on the label.\u003cbr\u003e The sealed strips have a shelf life of 24 months from the date of manufacture.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Pack of 25 sensors.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCode\u003c\/b\u003e 48528\u003c\/div\u003e","brand":"A.MENARINI DIAGNOSTICS","offers":[{"title":"Default Title","offer_id":45799809253643,"sku":"938766538","price":12.37,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_a0438e20-7015-4314-8b9a-3c878be562c9.jpg?v=1724845685"},{"product_id":"strisce-misurazione-chetonemia-glucomen-areo-b-ketone-sensor-10-pezzi","title":"GLUCOMEN AREO B-KETONE BLOOD KETONE TEST STRIPS 10 COUNT","description":"\u003ch1\u003eGlucoMen\u003cbr\u003e areo \u003ci\u003eB-Ketone Sensor\u003c\/i\u003e\n\n\u003c\/h1\u003e \u003cdiv align=\"justify\"\u003e\n\n\u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eIn vitro\u003c\/i\u003e medical-diagnostic device.\u003cbr\u003e Sensors for self-monitoring of ketonemia with the GlucoMen areo 2K instrument.\u003cbr\u003e These sensors are indicated for the quantitative determination of beta-hydroxybutyrate (BOHB or beta-ketone) in fresh capillary whole blood.\u003cbr\u003e Use GlucoMen areo Beta-Ketone Sensors exclusively with the GlucoMen areo 2K instrument.\u003cbr\u003e The GlucoMen areo 2K system is designed for monitoring and self-monitoring of blood glucose and beta-ketone levels at home and can also be used in hospitals by medical and healthcare personnel.\u003cbr\u003e The system is not intended for use in the diagnosis or screening of ketonemia (DKA) or for use in neonates.\u003cbr\u003e Do not change therapy based on ketonemia test results without first consulting your doctor or healthcare professional.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eGeneral characteristics\u003c\/b\u003e\u003cbr\u003e \u003ctable border=\"1cellspacing=0cellpadding=1\" width=\"550\"\u003e \u003ctr\u003e\n\n\u003ctd\u003e\u003cb\u003eKetonemia measurement\u003c\/b\u003e\u003c\/td\u003e\n\n\u003ctd align=\"Center\"\u003ebeta-hydroxybutyrate (BOHB or beta-ketone) in blood\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003e\u003cb\u003eEnzymatic composition (per cm\u003csup\u003e2\u003c\/sup\u003e of a test strip for ketonemia measurement\u003c\/b\u003e\u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e- D-3-hydroxybutyrate dehydrogenase (\u003ci\u003ePseudomonas sp.\u003c\/i\u003e) 1.5% w\/w\u003cbr\u003e - coenzyme (NAD+), 0.7% w\/w\u003cbr\u003e - redox mediator: 1,10-phenanthroline-5,6-dione, 20.0% w\/w\u003cbr\u003e - non-reactive substances: 77.8% w\/w\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\u003ctd colspan=\"2\"\u003e\u003cb\u003eUnit of measurement\u003c\/b\u003e\u003c\/td\u003e\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eBeta-ketone\u003c\/td\u003e\n\n\u003ctd align=\"Center\"\u003emmol\/L (not modifiable)\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\u003ctd colspan=\"2\"\u003e\u003cb\u003eMeasurement range\u003c\/b\u003e\u003c\/td\u003e\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eBeta-ketone\u003c\/td\u003e\n\n\u003ctd align=\"Center\"\u003e0.1-8.0 mmol\/L\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\u003ctd colspan=\"2\"\u003e\u003cb\u003eResponse time\u003c\/b\u003e\u003c\/td\u003e\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eBeta-ketone\u003c\/td\u003e\n\n\u003ctd align=\"Center\"\u003e8 seconds\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\u003ctd colspan=\"2\"\u003e\u003cb\u003eSample volume\u003c\/b\u003e\u003c\/td\u003e\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eBeta-ketone\u003c\/td\u003e\n\n\u003ctd align=\"Center\"\u003e0.8 microL\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\u003ctd colspan=\"2\"\u003e\u003cb\u003eHematocrit acceptability range\u003c\/b\u003e\u003c\/td\u003e\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eBeta-ketone\u003c\/td\u003e\n\n\u003ctd align=\"Center\"\u003eautomatically compensates the measurement based on hematocrit in the range 20-60%\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003e\u003cb\u003eCalibration and traceability\u003c\/b\u003e\u003c\/td\u003e\n\n\u003ctd align=\"Center\"\u003ethe GlucoMen areo 2K system has been calibrated against plasma reference values determined using a Stanbio Beta-Hydroxybutyrate LiquiColor procedure, Procedure No. 2440 (Stanbio Laboratory, 1261 North Main Street, Boerne, Texas 78006). The analyzer employing the Stanbio kit (secondary reference measurement procedure) has been calibrated with a series of standards containing beta-hydroxybutyrate (primary calibrators) prepared by gravimetric method at Stanbio Laboratory.\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003e\u003cb\u003eSample\u003c\/b\u003e\u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003efresh capillary whole blood\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003e\u003cb\u003eSensor coding\u003c\/b\u003e\u003c\/td\u003e\n\n\u003ctd align=\"Center\"\u003enot required\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003e\u003cb\u003eHygiene\u003c\/b\u003e\u003c\/td\u003e\n\n\u003ctd align=\"Center\"\u003eautomatic test strip ejection using a dedicated ejection button\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003e\u003cb\u003eSampling\u003c\/b\u003e\u003c\/td\u003e\n\n\u003ctd align=\"Center\"\u003eautomatic aspiration of the blood sample by capillarity\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\u003ctd colspan=\"2\"\u003e\u003cb\u003eOperating environment\u003c\/b\u003e\u003c\/td\u003e\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eBeta-ketone\u003c\/td\u003e\n\n\u003ctd align=\"Center\"\u003etemperature range: 10-40°C\u003cbr\u003e relative humidity: \u0026lt;85%\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003c\/table\u003e \u003cbr\u003e \u003cb\u003eInstructions for use\u003c\/b\u003e\u003cbr\u003e 1. Insert a new GlucoMen areo Beta-Ketone Sensor (light purple color) into the sensor insertion slot. The drop symbol will start flashing on the display and the ketone symbol Keth will appear at the bottom left. If nothing appears on the display, remove the sensor, reinsert it into the slot and wait for the drop symbol to start flashing.\u003cbr\u003e 2. Hold the tip of the sensor against the blood drop until the control window is filled. An acoustic signal will sound (if enabled) and the display will show a countdown.\u003cbr\u003e 3. Read the test results. An acoustic signal will announce the appearance of the test result on the screen with the ketone symbol Keth. The symbol will flash until the instrument turns off.\u003cbr\u003e 4. To remove the sensor, press the eject button. The instrument will turn off.\u003cbr\u003e Do not use GlucoMen areo Beta-Ketone Sensors to test samples taken from alternative sites: use only fresh capillary blood taken from fingertips.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e GlucoMen areo Beta-Ketone Sensors are for in vitro diagnostic use only (for external use only).\u003cbr\u003e Results may be incorrect if the patient is dehydrated, severely hypertensive, in shock or in a hyperosmolar state.\u003cbr\u003e Do not test critically ill patients.\u003cbr\u003e If the blood ketonemia test results are not compatible with the patient's perceived health status despite following all instructions in the GlucoMen areo 2K instrument's user manual, contact your doctor or healthcare provider.\u003cbr\u003e Never make significant changes to your diabetes management plan without first discussing it with your doctor.\u003cbr\u003e Keep the instrument, sensors and other system components out of reach of children. Small parts can pose a choking hazard.\u003cbr\u003e Handle sensors with clean, dry hands.\u003cbr\u003e Dispose of used lancets (needles) and sensors in accordance with local regulations.\u003cbr\u003e Handling blood can be dangerous; exercise extreme caution when handling blood, sensors, lancets (needles) and the instrument.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eStorage\u003c\/b\u003e\u003cbr\u003e Store the aluminum blister pack of sensors at a temperature of 4-30°C; do not freeze or refrigerate.\u003cbr\u003e Avoid exposure to humidity, heat and direct sunlight. Do not use sensors beyond the expiration date as this may lead to incorrect results.\u003cbr\u003e Check the expiration date on the aluminum blister pack.\u003cbr\u003e GlucoMen areo Beta-Ketone Sensors are individually packaged in aluminum blister packs, with a validity of 18 months from the date of manufacture.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Pack of 10 pieces.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCode\u003c\/b\u003e 48530\u003c\/div\u003e","brand":"A.MENARINI DIAGNOSTICS","offers":[{"title":"Default Title","offer_id":45799809876235,"sku":"938766565","price":15.37,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_c1740c7c-185e-4ae7-bf11-7f220d27a0bc.jpg?v=1724845693"},{"product_id":"screen-test-rapido-streptococco-tampone-faringeo-screen-2-pezzi-self-test-strep-a","title":"SCREEN RAPID STREPTOCOCCUS THROAT SWAB SCREEN 2 PIECES SELF TEST STREP A","description":"\u003ch1\u003eSCREEN STEP-A\u003c\/h1\u003e \u003cdiv align=\"justify\"\u003e \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e The Strep A rapid test is a rapid immunochromatographic test for the qualitative detection of Strep A antigens in pharyngeal swab samples to aid in the diagnosis of Group A Streptococcus infections.\u003cbr\u003e Early diagnosis and treatment of Group A strep pharyngitis infections will reduce the severity of symptoms and further complications such as rheumatic fever and glomerulonephritis, which is why it would be useful to have a test at hand at home to be able to make a diagnosis at the onset of the first symptoms.\u003cbr\u003e When the sample is added to the appropriate well, capillary action induces the sample to migrate through the membrane. When the levels of Group A streptococcal antigen in the samples are equal to or greater than the cut-off, a visible colored line appears in the test zone, which indicates a positive result. The absence of such a colored line in the Test (T) zone suggests a negative result.\u003cbr\u003e If the test has been performed correctly, a colored line will appear on the control zone (C) as a procedural control.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eInstructions for use\u003c\/b\u003e\u003cbr\u003e \u003cu\u003eSample collection and preparation\u003c\/u\u003e\u003cbr\u003e 1. Collect the sample with the sterile pharyngeal swab provided in the kit.\u003cbr\u003e 2. Hold down the tongue with a tongue depressor. Swab the back of the pharynx, tonsils and other inflamed areas. Avoid touching the tongue, cheeks and teeth with the swab.\u003cbr\u003e 3. The test should ideally be performed immediately after sample collection.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eProcedure\u003c\/u\u003e\u003cbr\u003e Bring the device and extraction reagents to room temperature (10 °C-30 °C) before performing the test.\u003cbr\u003e 1. Add 4 drops of extraction reagent A and 4 drops of reagent B to the respective extraction tube and mix thoroughly.\u003cbr\u003e 2. Place the sample extraction swab in the tube.\u003cbr\u003e Shake the swab ten times. Leave the swab in the tube for one minute. Then remove the swab while squeezing the head of the swab against the inside of the tube as you remove it to eliminate as much liquid as possible from the swab. Discard the swab.\u003cbr\u003e 3. Cap the tube and mix the contents by gently shaking.\u003cbr\u003e The sample must be tested immediately.\u003cbr\u003e 4. Remove the test from the sealed aluminum pouch by tearing where there is the notch and place the test on a clean, dry and flat surface. Add 3 drops of mixed liquid sample from the tube to the sample well (depicting an arrow) of the test cassette by inverting and squeezing the tube.\u003cbr\u003e 5. Wait 10 minutes and read the results. Do not read the results after 15 minutes.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eReading the results\u003c\/b\u003e\u003cbr\u003e Positive\u003cbr\u003e If two colored lines are visible in both the test zone (T) and the control zone (C), the result is positive. It indicates that you may be in a Strep A infection phase and you should consult your doctor.\u003cbr\u003e Negative\u003cbr\u003e If only one colored line appears in the control zone (C) and no colored line appears in the test strip (T), the result is negative. It indicates that the concentration of Group A streptococcal antigen is equal to or below the detection limit of the test.\u003cbr\u003e Invalid\u003cbr\u003e No line visible or only one line visible in the test zone but not in the control zone. This is an indication of procedural error and\/or that deterioration of the test reagent has occurred. Repeat the test with a new kit. If the test is still invalid, please contact the distributor or the store where you purchased the product, providing the batch number.\u003cbr\u003e \u003cbr\u003e \u003cb\u003ePrecautions\u003c\/b\u003e\u003cbr\u003e 1. This kit is for in vitro self-diagnostic use only. Do not ingest.\u003cbr\u003e 2. Do not swap caps between reagents.\u003cbr\u003e 3. Do not use the test beyond the expiration date.\u003cbr\u003e 4. Keep out of reach of children.\u003cbr\u003e 5. Do not use the test if the pouch is punctured or not well sealed.\u003cbr\u003e 6. Discard after use. The test is for single use.\u003cbr\u003e 7. Avoid contact of reagents A and B with eyes, sensitive mucous membranes, membranes, cuts, abrasions, etc. If these reagents come into contact with skin or eyes, rinse thoroughly with water.\u003cbr\u003e 8. Do not eat, drink or smoke in the area where the samples are located and where the test will be performed.\u003cbr\u003e 9. Protective gloves should be worn when handling the sample. Wash hands thoroughly after the procedure.\u003cbr\u003e 10. The used device, swab and extraction tube must be treated as contagious waste and therefore discarded in containers for biohazardous items.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eLimitations\u003c\/b\u003e\u003cbr\u003e 1. The results of this test should not be used to determine pharyngitis infections, as pharyngitis can be caused by organisms other than Group A streptococcus. This test provides no information on pharyngitis other than that caused by Group A streptococcal infection.\u003cbr\u003e 2. A negative result may occur due to an insufficient amount of sample collected, or insufficient addition of reagent A and B. If symptoms persist or worsen, always consult your doctor.\u003cbr\u003e 3. Excess blood or mucus in the collected sample could interfere with test performance and could lead to a false positive result. Do not touch the tongue, cheeks, teeth or any bleeding areas of the mouth with the swab during the sample collection phase.\u003cbr\u003e 4. As with any diagnostic procedure, a diagnosis should be confirmed exclusively by a doctor after evaluating all clinical and laboratory results.\u003cbr\u003e 5. Since a toxic composition is present in the test kit and the highest morbidity rate from upper respiratory tract infections has been found in children, the test should be performed by parents or another adult family member on all minors under 16 years of age.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eStorage\u003c\/b\u003e\u003cbr\u003e Store between 4 °C and 30 °C in the sealed package until the expiration date. Keep away from sunlight, humidity and heat. Do not freeze. Preferably open the pouch just before performing the test.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Pack containing:\u003cbr\u003e 2 individually sealed pouches, each containing:\u003cbr\u003e - test device;\u003cbr\u003e - desiccant pouch.\u003cbr\u003e The desiccant is for storage purposes only, it is not used during the test procedure.\u003cbr\u003e 2 extraction tubes.\u003cbr\u003e 2 sterile pharyngeal swabs. The swab is used to collect the sample.\u003cbr\u003e Extraction reagents A and B (attention: reagent B is toxic if ingested).\u003cbr\u003e Leaflet with instructions for use.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCod.\u003c\/b\u003e 971664533\u003c\/div\u003e","brand":"SCREEN ITALIA Srl","offers":[{"title":"Default Title","offer_id":45800050327819,"sku":"971664533","price":9.09,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_b10af392-f000-43e0-888f-420367e04f94.jpg?v=1724849947"},{"product_id":"test-one-step-strep-a-autodiagnostico-determinazione-qualitativa-antigeni-streptococco-a-da-tampone-faringeo","title":"STREP A TEST ONE STEP AUTODIAGNOSTIC QUALITATIVE DETERMINATION OF STREPTOCOCCUS A ANTIGENS FROM THROAT SWAB","description":"\u003ch2\u003eSCREEN\u003c\/h2\u003e \u003ch1\u003eStrep A\u003c\/h1\u003e \u003cdiv align=\"justify\"\u003e \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e Immunological lateral flow test for the qualitative detection of Group A Streptococcus antigen from throat swab samples to aid in the early diagnosis of Group A Streptococcus infection.\u003cbr\u003e When the sample is added to the dedicated well, capillary action causes the sample to migrate across the membrane. When the levels of Strep A antigen in the samples are equal to or above the cut-off, a visible colored line appears in the test zone, indicating a positive result. The absence of such a colored line in the test zone suggests a negative result. If the test has been performed correctly, a colored line will appear in the control zone as a procedural control method.\u003cbr\u003e For in vitro self-testing.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eInstructions for use\u003c\/b\u003e\u003cbr\u003e \u003cu\u003eSample collection and preparation\u003c\/u\u003e\u003cbr\u003e Collect the sample with the sterile throat swab provided in the kit. Hold the tongue down with a tongue depressor. Swab the back of the pharynx, tonsils, and other inflamed areas. Avoid touching the tongue, cheeks, and teeth with the swab.\u003cbr\u003e The test should ideally be performed immediately after sample collection.\u003cbr\u003e \u003cbr\u003e \u003cu\u003ePerforming the test\u003c\/u\u003e\u003cbr\u003e Bring the device and extraction reagents to room temperature (10-30 °C) before performing the test.\u003cbr\u003e Add 4 drops of extraction reagent A and 4 drops of reagent B into the respective extraction tube and mix thoroughly.\u003cbr\u003e Place the extraction swab into the tube. Shake the swab ten times. Leave the swab in the tube for 1 minute. Then remove the swab while squeezing the swab head against the walls of the tube to release as much liquid as possible into the tube. Dispose of the used swab.\u003cbr\u003e Remove the test from the sealed foil pouch, tearing at the notch, and place the test on a clean, dry, flat surface.\u003cbr\u003e Add 3 drops of extracted sample into the sample well on the test cassette.\u003cbr\u003e Wait 10 minutes and read the results. Do not read the results after 15 minutes.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eInterpretation of results\u003c\/u\u003e\u003cbr\u003e POSITIVE: two colored lines appear, one in the test zone (T) and one in the control zone (C). A Group A Streptococcus infection may be present; it is advisable to consult your doctor.\u003cbr\u003e \u003cbr\u003e NEGATIVE: only one colored line appears in the control zone (C). No colored line appears in the test zone (T). The concentration of Group A Streptococcus antigen is at or below the detection limit of the test.\u003cbr\u003e \u003cbr\u003e INVALID: no colored line appears or only one colored line appears in the test zone (T) and no colored line appears in the control zone (C). The failure of the control line (C) to appear indicates that an error occurred during the test procedure or that the test reagent has deteriorated. Repeat the test again with a new kit. If the test gives an invalid result again, contact the local distributor.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e For in vitro self-diagnostic use only.\u003cbr\u003e Do not ingest.\u003cbr\u003e Do not swap caps between reagents.\u003cbr\u003e Do not use the test beyond the expiration date.\u003cbr\u003e Keep out of reach of children.\u003cbr\u003e Do not use the test if the package is punctured or not well sealed.\u003cbr\u003e The test is for single use: dispose of after use.\u003cbr\u003e Avoid contact of reagents A and B with eyes, sensitive mucous membranes, membranes, cuts, abrasions, etc. If reagents come into contact with skin or eyes, rinse thoroughly with water.\u003cbr\u003e Do not eat, drink, or smoke in the area where samples are handled and where the test is performed.\u003cbr\u003e The used device, swab, and extraction tube should be treated as infectious waste and therefore disposed of in biohazard waste containers.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eStorage\u003c\/b\u003e\u003cbr\u003e Store at 4-30 °C. Keep away from sunlight, humidity, and heat. Do not freeze.\u003cbr\u003e Shelf life unopened: 24 months.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e The kit contains:\u003cbr\u003e - 1 sealed pouch (containing one test device and one desiccant pouch);\u003cbr\u003e - 1 extraction tube;\u003cbr\u003e - 1 sterile throat swab;\u003cbr\u003e - extraction reagents A and B;\u003cbr\u003e - instructions for use.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCode\u003c\/b\u003e W039P0001\u003c\/div\u003e","brand":"SCREEN ITALIA Srl","offers":[{"title":"Default Title","offer_id":45800590475531,"sku":"987318110","price":3.95,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_1d5954aa-a365-4699-a3f1-81eecc439610.jpg?v=1724858576"},{"product_id":"screen-test-rapido-streptococco-tampone-faringeo-screen-2-pezzi","title":"RAPID STREPTOCOCCUS SCREEN TEST PHARYNGEAL SWAB SCREEN 2 PIECES","description":"\u003ch1\u003eSCREEN STEP-A\u003c\/h1\u003e \u003cdiv align=\"justify\"\u003e \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e The Strep A rapid test is a rapid immunochromatographic test for the qualitative detection of Strep A antigens in throat swab samples to aid in the diagnosis of Group A Streptococcus infections.\u003cbr\u003e Early diagnosis and treatment of Group A strep pharyngitis infections will reduce the severity of symptoms and further complications such as rheumatic fever and glomerulonephritis, which is why it would be useful to have a test at hand at home to be able to make a diagnosis at the onset of the first symptoms.\u003cbr\u003e When the sample is added to the sample well, capillary action causes the sample to migrate through the membrane. When the levels of Group A streptococcal antigen in the samples are equal to or greater than the cut-off, a visible coloured line appears in the test zone, indicating a positive result. The absence of such a coloured line in the Test (T) zone suggests a negative result.\u003cbr\u003e If the test has been performed correctly, a coloured line will appear in the control (C) zone as a procedural control.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eInstructions for use\u003c\/b\u003e\u003cbr\u003e \u003cu\u003eSample collection and preparation\u003c\/u\u003e\u003cbr\u003e 1. Collect the sample with the sterile throat swab provided in the kit.\u003cbr\u003e 2. Hold down the tongue with a tongue depressor. Swab the back of the pharynx, tonsils, and other inflamed areas. Avoid touching the tongue, cheeks, and teeth with the swab.\u003cbr\u003e 3. The test should ideally be performed immediately after sample collection.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eProcedure\u003c\/u\u003e\u003cbr\u003e Bring the device and extraction reagents to room temperature (10°C-30°C) before performing the test.\u003cbr\u003e 1. Add 4 drops of extraction reagent A and 4 drops of reagent B into the respective extraction tube and mix completely.\u003cbr\u003e 2. Place the sample extraction swab into the tube.\u003cbr\u003e Agitate the swab ten times. Leave the swab in the tube for one minute. Then remove the swab while squeezing the head of the swab against the inside of the tube as you remove it to eliminate as much liquid as possible from the swab. Discard the swab.\u003cbr\u003e 3. Cap the tube and mix the contents by gently shaking.\u003cbr\u003e The sample must be tested immediately.\u003cbr\u003e 4. Remove the test from the sealed foil pouch by tearing where there is the notch and place the test on a clean, dry, flat surface. Add 3 drops of mixed liquid sample from the tube to the sample well (depicting an arrow) of the test cassette by inverting and squeezing the tube.\u003cbr\u003e 5. Wait 10 minutes and read the results. Do not read the results after 15 minutes.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eReading the results\u003c\/b\u003e\u003cbr\u003e Positive\u003cbr\u003e If two coloured lines are visible in both the test zone (T) and the control zone (C), the result is positive. It indicates that you may be in a Strep A infection phase and you should consult your doctor.\u003cbr\u003e Negative\u003cbr\u003e If only one coloured line appears in the control zone (C) and no coloured line appears in the test band (T), the result is negative. It indicates that the concentration of Group A streptococcal antigen is at or below the detection limit of the test.\u003cbr\u003e Invalid\u003cbr\u003e No line visible or only one line visible in the test zone but not in the control zone. This is an indication of procedural error and\/or that deterioration of the test reagent has occurred. Repeat the test with a new kit. If the test is still invalid, please contact the distributor or the shop where you purchased the product, providing the lot number.\u003cbr\u003e \u003cbr\u003e \u003cb\u003ePrecautions\u003c\/b\u003e\u003cbr\u003e 1. This kit is for in vitro self-diagnostic use only. Do not ingest.\u003cbr\u003e 2. Do not swap caps between reagents.\u003cbr\u003e 3. Do not use the test beyond the expiry date.\u003cbr\u003e 4. Keep out of reach of children.\u003cbr\u003e 5. Do not use the test if the pouch is perforated or not well sealed.\u003cbr\u003e 6. Discard after use. The test is for single use.\u003cbr\u003e 7. Avoid contact of reagents A and B with eyes, sensitive mucous membranes, membranes, cuts, abrasions, etc. If these reagents come into contact with skin or eyes, rinse thoroughly with water.\u003cbr\u003e 8. Do not eat, drink or smoke in the area where samples are located and where the test will be performed.\u003cbr\u003e 9. Protective gloves should be worn when handling the sample. Wash hands thoroughly after the procedure.\u003cbr\u003e 10. The used device, swab and extraction tube should be treated as infectious waste and therefore disposed of in biohazard containers.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eLimitations\u003c\/b\u003e\u003cbr\u003e 1. The results of this test should not be used to determine pharyngitis infections, as pharyngitis can be caused by organisms other than Group A streptococcus. This test does not provide any information about pharyngitis other than that caused by Group A streptococcal infection.\u003cbr\u003e 2. A negative result may occur due to an insufficient amount of sample collected, or insufficient addition of reagent A and B. If symptoms persist or intensify, always consult your doctor.\u003cbr\u003e 3. Excess blood or mucus in the collected sample may interfere with the test performance and could lead to a false positive result. Do not touch the tongue, cheeks, teeth or any bleeding areas of the mouth with the swab during the sample collection phase.\u003cbr\u003e 4. As with any diagnostic procedure, a diagnosis should only be confirmed by a doctor after evaluating all clinical and laboratory results.\u003cbr\u003e 5. Since the test kit contains a toxic composition and the highest morbidity rate from upper respiratory tract infections has been found in children, the test should be performed by parents or another adult family member on all minors under 16 years of age.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eStorage\u003c\/b\u003e\u003cbr\u003e Store between 4 °C and 30 °C in the sealed packaging until the expiry date. Keep away from sunlight, humidity and heat. Do not freeze. Preferably open the pouch just before performing the test.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Pack containing:\u003cbr\u003e 2 individually sealed pouches, each containing:\u003cbr\u003e - test device;\u003cbr\u003e - desiccant pouch.\u003cbr\u003e The desiccant is for storage purposes only, it is not used during the test procedure.\u003cbr\u003e 2 extraction tubes.\u003cbr\u003e 2 sterile throat swabs. The swab is used to collect the sample.\u003cbr\u003e Extraction reagents A and B (caution: reagent B is toxic if ingested).\u003cbr\u003e Package leaflet with instructions for use.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCode\u003c\/b\u003e 971664533\u003c\/div\u003e","brand":"SCREEN ITALIA Srl","offers":[{"title":"Default Title","offer_id":45878504456459,"sku":"971664533","price":9.09,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_58e286c2-cf84-481e-8b6b-aa0681f3ed03.jpg?v=1726636510"},{"product_id":"contenitore-urine-alvita-prontotest-prelievo-sottovuoto-120-ml-1-pezzo","title":"ALVITA PRONTOTEST URINE CONTAINER VACUUM COLLECTION 120 ML 1 PIECE","description":"\u003ch1\u003eALVITA PRONTOTEST URINE CONTAINER VACUUM COLLECTION 120 ML 1 PIECE\u003c\/h1\u003e","brand":"ALLIANCE HEALTHCARE IT.DIS.SpA","offers":[{"title":"Default Title","offer_id":45889068630283,"sku":"932078330","price":0.46,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_7e85c3d5-17ab-402e-8a18-6550f726cdc2.jpg?v=1726808973"},{"product_id":"screen-test-rapido-streptococco-tampone-faringeo-2-pezzi","title":"RAPID STREPTOCOCCUS SCREEN TEST THROAT SWAB 2 PIECES","description":"\u003ch1\u003eSCREEN STEP-A\u003c\/h1\u003e \u003cdiv align=\"justify\"\u003e \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e The Strep A rapid test is a rapid immunochromatographic test for the qualitative detection of Strep A antigens in pharyngeal swab samples to aid in the diagnosis of Group A Streptococcus infections.\u003cbr\u003e Early diagnosis and treatment of Group A streptococcal pharyngitis infections will reduce the severity of symptoms and further complications such as rheumatic fever and glomerulonephritis. Therefore, it would be useful to have a test at hand at home to be able to make a diagnosis at the onset of the first symptoms.\u003cbr\u003e When the sample is added to the appropriate well, capillary action causes the sample to migrate through the membrane. When the levels of Group A streptococcal antigen in the samples are equal to or greater than the cut-off, a visible colored line appears in the test zone, indicating a positive result. The absence of such a colored line in the Test (T) zone suggests a negative result.\u003cbr\u003e If the test has been performed correctly, a colored line will appear in the control (C) zone as a procedural control.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eInstructions for use\u003c\/b\u003e\u003cbr\u003e \u003cu\u003eSample collection and preparation\u003c\/u\u003e\u003cbr\u003e 1. Collect the sample with the sterile pharyngeal swab provided in the kit.\u003cbr\u003e 2. Hold the tongue down with a tongue depressor. Swab the back of the pharynx, tonsils, and other inflamed areas. Avoid touching the tongue, cheeks, and teeth with the swab.\u003cbr\u003e 3. The test should ideally be performed immediately after sample collection.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eProcedure\u003c\/u\u003e\u003cbr\u003e Bring the device and extraction reagents to room temperature (10 °C-30 °C) before performing the test.\u003cbr\u003e 1. Add 4 drops of extraction reagent A and 4 drops of reagent B into the respective extraction tube and mix completely.\u003cbr\u003e 2. Place the sample extraction swab into the tube.\u003cbr\u003e Shake the swab ten times. Leave the swab in the tube for one minute. Then remove the swab while pressing the swab head against the inside of the tube as you remove it to eliminate as much liquid as possible from the swab. Discard the swab.\u003cbr\u003e 3. Cap the tube and mix the contents by gently shaking.\u003cbr\u003e The sample must be tested immediately.\u003cbr\u003e 4. Remove the test from the sealed aluminum pouch by tearing at the notch and place the test on a clean, dry, flat surface. Add 3 drops of mixed liquid sample from the tube to the sample well (depicting an arrow) of the test cassette by inverting and squeezing the tube.\u003cbr\u003e 5. Wait 10 minutes and read the results. Do not read the results after 15 minutes.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eReading the results\u003c\/b\u003e\u003cbr\u003e Positive\u003cbr\u003e If two colored lines are visible in both the test (T) zone and the control (C) area, the result is positive. It indicates that you may be in a Strep A infection phase and you should consult your doctor.\u003cbr\u003e Negative\u003cbr\u003e If only one colored line appears in the control (C) zone and no colored line appears in the test (T) band, the result is negative. It indicates that the concentration of Group A streptococcal antigen is equal to or below the detection limit of the test.\u003cbr\u003e Invalid\u003cbr\u003e No visible line or only one visible line in the test zone but not in the control zone. This is an indication of procedural error and\/or that deterioration of the test reagent has occurred. Repeat the test with a new kit. If the test is still invalid, please contact the distributor or the store where you purchased the product, providing the lot number.\u003cbr\u003e \u003cbr\u003e \u003cb\u003ePrecautions\u003c\/b\u003e\u003cbr\u003e 1. This kit is for in vitro self-diagnostic use only. Do not swallow.\u003cbr\u003e 2. Do not swap caps between reagents.\u003cbr\u003e 3. Do not use the test beyond the expiration date.\u003cbr\u003e 4. Keep out of reach of children.\u003cbr\u003e 5. Do not use the test if the pouch is perforated or not well sealed.\u003cbr\u003e 6. Discard after use. The test is single-use.\u003cbr\u003e 7. Avoid contact of reagents A and B with eyes, sensitive mucous membranes, membranes, cuts, abrasions, etc. If these reagents come into contact with skin or eyes, rinse thoroughly with water.\u003cbr\u003e 8. Do not eat, drink or smoke in the area where samples are located and where the test will be performed.\u003cbr\u003e 9. Protective gloves should be worn when handling the sample. Wash hands thoroughly after the procedure.\u003cbr\u003e 10. The used device, swab, and extraction tube should be treated as infectious waste and therefore discarded in biohazard containers.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eLimitations\u003c\/b\u003e\u003cbr\u003e 1. The results of this test should not be used to determine pharyngitis infections, as pharyngitis can be caused by organisms other than Group A streptococcus. This test provides no information on pharyngitis other than that caused by Group A streptococcal infection.\u003cbr\u003e 2. A negative result may occur due to an insufficient amount of sample collected, or insufficient addition of reagents A and B. If symptoms persist or worsen, always consult your doctor.\u003cbr\u003e 3. Excess blood or mucus in the collected sample could interfere with test performance and could lead to a false positive result. Do not touch the tongue, cheeks, teeth, or any bleeding areas of the mouth with the swab during the sample collection phase.\u003cbr\u003e 4. As with any diagnostic procedure, a diagnosis should be confirmed exclusively by a doctor after evaluating all clinical and laboratory results.\u003cbr\u003e 5. Since the test kit contains a toxic composition and the highest morbidity rate from upper respiratory tract infections has been found in children, the test should be performed by parents or another adult family member on all minors under 16 years of age.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eStorage\u003c\/b\u003e\u003cbr\u003e Store between 4 °C and 30 °C in the sealed packaging until the expiration date. Keep away from sunlight, humidity and heat. Do not freeze. Preferably open the pouch just before performing the test.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Pack containing:\u003cbr\u003e 2 individually sealed pouches, each containing:\u003cbr\u003e - test device;\u003cbr\u003e - desiccant sachet.\u003cbr\u003e The desiccant is for storage purposes only, it is not used during the test procedure.\u003cbr\u003e 2 extraction tubes.\u003cbr\u003e 2 sterile pharyngeal swabs. The swab is used to collect the sample.\u003cbr\u003e Extraction reagents A and B (attention: reagent B is toxic if ingested).\u003cbr\u003e Package insert with instructions for use.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCode\u003c\/b\u003e 971664533\u003c\/div\u003e","brand":"SCREEN ITALIA Srl","offers":[{"title":"Default Title","offer_id":45914871824651,"sku":"971664533","price":9.09,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_80111c38-9fab-4bd7-8f76-bd77d1872397.jpg?v=1727241285"},{"product_id":"wellion-luna-50-strips-strisce-per-misurazione-glicemia","title":"WELLION LUNA 50 STRIPS GLUCOSE TEST STRIPS","description":"\u003ch1\u003eWellion\u003c\/h1\u003e \u003ch2\u003e Luna\u003c\/h2\u003e \u003cdiv align=\"justify\"\u003e\n\n\u003cb\u003e Description\u003c\/b\u003e\u003cbr\u003e Wellion Luna blood glucose test strips are used with Wellion Luna series meters to measure blood glucose levels in whole blood.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eInstructions for use\u003c\/b\u003e\u003cbr\u003e When the tip of the Wellion blood glucose test strip touches a drop of capillary whole blood on the finger, the blood reaches the reaction area. The measurement time is less than 5 seconds and a minimal amount of blood is required. The test result for blood glucose levels will be displayed on the Wellion Luna series meters' display. The Wellion Luna blood glucose test strip measures glucose from 20 mg\/dL (1.1 mmol\/l) to 600 mg\/dL (33.3 mmol\/l).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e \u003cbr\u003ePack of 50 pieces.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCode\u003c\/b\u003e WELL615\u003c\/div\u003e","brand":"MED TRUST ITALIA Srl","offers":[{"title":"Default Title","offer_id":45941727297803,"sku":"925606865","price":22.46,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_bff6f2b4-a8df-4d84-ac2d-e7c95eb481fc.jpg?v=1727793618"},{"product_id":"screen-test-leucociti-sangue-nitrito-e-proteina-urina-screen-test-infezioni-vie-urinarie-3-pezzi","title":"BLOOD LEUKOCYTE SCREEN TEST URINE NITRITE AND PROTEIN URINARY TRACT INFECTION SCREEN TEST 3 PIECES","description":"\u003ch1\u003eSCREEN\u003cbr\u003e CHECK TEST\u003c\/h1\u003e \u003cb\u003eUrinary Tract Infections\u003c\/b\u003e\u003cbr\u003e \u003cbr\u003e \u003cdiv align=\"justify\"\u003e\n\n\u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e CE 0123 In vitro diagnostic medical device. \u003cbr\u003e Rapid test for the qualitative rapid detection of Leukocytes, Blood, Nitrite and Protein in human urine.\u003cbr\u003e For in vitro self-diagnostic use only.\u003cbr\u003e \u003cbr\u003e \u003cb\u003ePrecautions\u003c\/b\u003e\u003cbr\u003e 1. For in vitro self-diagnostic use only.\u003cbr\u003e 2. Store in a dry place at 2-30°C (36-86°F), avoiding excessively humid areas. Do not use if the sealed package is damaged or open.\u003cbr\u003e 3. Keep out of reach of children.\u003cbr\u003e 4. Do not use after the expiry date or if the package is damaged.\u003cbr\u003e 5. Strictly follow the indicated timings.\u003cbr\u003e 6. Use the test only once. Do not disassemble or touch the reactive areas on the test strip.\u003cbr\u003e 7. For external use only.\u003cbr\u003e 8. The used test must be disposed of according to local regulations.\u003cbr\u003e 9. In case of difficulty in identifying colors (such as color blindness), seek help for reading the test.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eInstructions for use\u003c\/b\u003e\u003cbr\u003e It is advisable to collect a urine sample for the test early in the morning as it is the most concentrated. The urine used for the test should not come into contact with toilet water or any disinfectant or cleaning product.\u003cbr\u003e For women only: the test should not be performed during or within three days after the menstrual cycle. The urine sample should not be contaminated with vaginal fluids as they may produce misleading results.\u003cbr\u003e Do not make important medical decisions without first consulting your doctor.\u003cbr\u003e URINE COLLECTION: collect part of the urine in the provided plastic container or use a clean container free of detergent residues. Make sure to fill the container with urine.\u003cbr\u003e PERFORMING THE TEST:\u003cbr\u003e 1) open the sealed package and remove the test strip. Do not touch the test fields. Once the package is opened, it is advisable to perform the test immediately;\u003cbr\u003e 2) immerse the test strip in the urine sample. CAUTION: make sure that all four test fields are immersed for at least 1-2 seconds.\u003cbr\u003e 3) remove the test strip and remove excess urine by wiping it on the edge of the container or using absorbent material (e.g. a paper tissue) to avoid mixing chemicals from adjacent areas. Wait 2 minutes (do not read the results after 3 minutes).\u003cbr\u003e \u003cbr\u003e \u003cb\u003eReading the results\u003c\/b\u003e\u003cbr\u003e Color variations on the edges of the test pads or beyond 3 minutes should be ignored.\u003cbr\u003e NEGATIVE:\u003cbr\u003e - the LEUKOCYTE test field remained whitish;\u003cbr\u003e - the BLOOD test field remained yellow-orange;\u003cbr\u003e - the NITRITE test field remained white;\u003cbr\u003e - the PROTEIN test field remained yellowish.\u003cbr\u003e POSITIVE RESULT FOR LEUKOCYTES: if the color of the corresponding area has turned lilac, it means that leukocytes are present in the urine.\u003cbr\u003e POSITIVE RESULT FOR BLOOD: if the color of the corresponding area has turned green (or green dots have appeared at the bottom), it means that blood is present in the urine.\u003cbr\u003e POSITIVE RESULT FOR NITRITE: if the color of the corresponding area has turned pink, it means that nitrites are present in the urine.\u003cbr\u003e POSITIVE RESULT FOR PROTEIN: if the color of the corresponding area has turned green, it means that proteins are present in the urine.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eLimitations\u003c\/b\u003e\u003cbr\u003e The urinary tract infection test (Urine) can be affected by substances that cause abnormal urine color such as medications containing azo dyes, nitrofurantoin, and riboflavin1. Color development on the test pad may be masked or the colored reaction may be interpreted as a false result.\u003cbr\u003e Leukocytes: the result should be read at 2 minutes to allow for full color development. The intensity of the color that develops is proportional to the number of leukocytes present in the urine sample. Highly proteinaceous urine can lower the intensity of the color reaction. This test does not react with erythrocytes or common bacteria in urine.\u003cbr\u003e Blood: a uniform green color indicates the presence of myoglobin, hemoglobin, or hemolyzed erythrocytes1. Scattered or compact green dots indicate intact erythrocytes. To improve accuracy, separate color scales are provided for hemoglobin and erythrocytes. Positive test results are often observed in the urine of women during menstruation. It has been reported that high pH urine reduces sensitivity, while a moderate to high concentration of ascorbic acid can inhibit color formation.\u003cbr\u003e Microbial peroxidase, associated with urinary tract infections, can cause false positives. The test is slightly more sensitive to free hemoglobin and myoglobin than to intact erythrocytes.\u003cbr\u003e Nitrite: the test is specific for nitrite and will not react with any other substance normally excreted in urine. Any degree of uniform pink or red should be interpreted as a positive result, suggesting the presence of nitrite. The intensity of the color is not proportional to the number of bacteria present in the urine sample. Pink dots or edges should not be considered a positive result. Comparing the test with a white background can help detect low levels of nitrite that might otherwise not be detected. The sensitivity of this test is reduced for urine samples with highly buffered alkaline urine with high specific gravity. A negative result in no way rules out the possibility of bacteriuria. Negative results can be obtained with urinary tract infections caused by organisms that do not contain reductase that converts nitrate to nitrite; nitrate does not convert to nitrite when urine has not remained sufficiently in the bladder (at least 4 hours); when undergoing antibiotic therapy or when nitrate is absent from the diet.\u003cbr\u003e Protein: any shade of green indicates the presence of protein in the urine. This test is highly sensitive to albumin and less sensitive to hemoglobin, globulin, and mucoprotein. A negative result does not exclude the presence of these or other proteins. False positives can be obtained with alkaline or highly buffered urine. Contamination of urine samples with quaternary ammonium compounds or body soaps containing chlorhexidine can produce false positive results. Urine samples with high specific gravity can give false negatives. \u003cbr\u003e \u003cbr\u003e \u003cb\u003eStorage\u003c\/b\u003e\u003cbr\u003e Store in the package at room temperature (2-30°C).\u003cbr\u003e The test is stable until the expiry date printed on the sealed package. The test should remain in the sealed package until use.\u003cbr\u003e DO NOT FREEZE.\u003cbr\u003e Do not use after the expiry date.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Pack containing 3 pieces.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eBIBLIOGRAPHY:\u003c\/u\u003e\u003cbr\u003e 1. Henry JB, et al. Clinical Diagnosis and Management by Laboratory Methods, 20th Ed. Philadelphia. Saunders. 371-372, 375, 379, 382, 385, 2001.\u003c\/div\u003e","brand":"SCREEN ITALIA Srl","offers":[{"title":"Default Title","offer_id":45942076145931,"sku":"926819184","price":8.89,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_f284e9bc-76fe-4260-a934-4caad6849063.jpg?v=1727797186"},{"product_id":"striscia-visiva-per-autoanalisi-in-urine-di-glucosio-leucociti-proteine-nitriti-e-sangue-combur-5-test-hc-10-pezzi","title":"COMBUR 5 TEST HC 10 PIECES VISUAL DIPSTICK FOR URINE SELF-TEST OF GLUCOSE LEUKOCYTES PROTEINS NITRITES AND BLOOD","description":"\u003ch1\u003eCombur \u003csup\u003e\u003cu\u003e5\u003c\/u\u003e\u003c\/sup\u003e\u003cbr\u003e Test\u003csup\u003e\u003cfont size=\"3\"\u003e®\u003c\/font\u003e\u003c\/sup\u003e HC \u003c\/h1\u003e Test strips for the determination of the following parameters:\u003cbr\u003e - glucose\u003cbr\u003e - leukocytes\u003cbr\u003e - protein\u003cbr\u003e - nitrites \u003cbr\u003e - blood \u003cbr\u003e in urine.\u003cbr\u003e Suitable for self-monitoring and for the early diagnosis and monitoring of kidney and urinary tract diseases, as well as diabetes mellitus.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCode\u003c\/b\u003e 0011896954176","brand":"ROCHE DIAGNOSTICS SpA","offers":[{"title":"Default Title","offer_id":45942124478731,"sku":"939676185","price":17.9,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_f5560129-5599-46ea-a6ce-e8b868eb6407.jpg?v=1727797445"},{"product_id":"xeliac-test-pro-determinazione-anticorpi-iga-e-igg-associati-alla-malattia-celiaca-1-pezzo","title":"XELIAC TEST FOR THE DETERMINATION OF IGA AND IGG ANTIBODIES ASSOCIATED WITH CELIAC DISEASE 1 PIECE","description":"\u003ch1\u003eXeliac Test Pro\u003c\/h1\u003e \u003cdiv align=\"justify\"\u003eDetects the presence of class A and class G anti-transglutaminase antibodies associated with celiac disease in a human blood sample. \u003cbr\u003e Celiac disease is a serious, lifelong gastrointestinal disorder that can cause a wide spectrum of symptoms such as diarrhea, abdominal distension, weight loss, malnutrition, and skin diseases. It is caused by a permanent intolerance to gluten, a complex of proteins found in wheat, barley, rye, many other cereals, and all foods containing them. In celiac subjects, gluten intolerance manifests with an immune response that involves the production of specific antibodies (IgA and IgG).\u003cbr\u003e Xeliac® Test Pro is used as a support in the diagnosis of celiac disease, which must be confirmed by a physician. During a gluten-free diet, both the symptoms and the level of IgA and IgG antibodies associated with celiac disease decrease. Often, a few weeks after changing the diet or at the latest within 6 weeks, the antibody level is no longer detectable. Therefore, if you are following a gluten-free diet, it is possible to get a negative result. The application of a gluten-free diet should only be done under the instructions of a physician.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eInstructions for use\u003c\/b\u003e\u003cbr\u003e XeliacR Test Pro is a simple, reliable, and rapid home self-test. A timer is required to perform XeliacR Test Pro. Perform the test in a well-lit area. The test requires only one drop (10 µl) of blood and can be read after 5 to 10 minutes from its execution. Sample collection is practically painless.\u003cbr\u003e 1. Remove the cassette from the aluminum pouch and place it on a dry, horizontal surface. The test must be performed within 10 minutes.\u003cbr\u003e 2. Prepare the plastic pipette and place it in an easily accessible position. \u003cbr\u003e 3. Take the lancet. Twist the safety cap and remove it completely. The lancet is ready for use. Do not use the lancet (sterile) if the safety cap is missing or tampered with.\u003cbr\u003e 4. Gently massage a fingertip.\u003cbr\u003e 5. Place the lancet on the side of the fingertip (in the areas indicated in the figure) on the side where the safety cap was housed and press. The prick is practically painless. Caution: apply slight pressure to the fingertip before activating the lancet.\u003cbr\u003e 6. Immediately squeeze the fingertip until an abundant drop of blood appears. Take the pipette, bring it close to the blood drop until it touches it. The blood will automatically flow into the pipette up to the signal indicated on the nozzle (capillary filling). Do not press the bulb during this operation.\u003cbr\u003e7. Once filled, squeeze the pipette, pressing on the bulb, into the hole of the cassette indicated by the arrow to empty it completely. If there is difficulty expelling all the blood, cover the ventilation hole on the nozzle with a finger.\u003cbr\u003e 8. Wait 60 seconds. In the meantime, apply the plaster to the fingertip.\u003cbr\u003e 9. Open the appropriate diluent nozzle (DIL) as described by the arrows and dispense 4 drops into the same hole where the pipette was previously emptied. Caution: Do not dispense more than 4 drops of diluent, otherwise the interpretation of the test may be difficult.\u003cbr\u003e 10. After performing this procedure, wait at least 5 minutes and then read the result. This result must appear within 10 minutes. After 10 minutes, the test is no longer reliable, whatever the result.\u003cbr\u003e 11. Interpretation of results.\u003cbr\u003e Negative result: only a blue transverse line appears near the letter C on the cassette. This line is the Control line and must always appear. In this case, the presence of celiac disease can be practically excluded. In the presence of gastrointestinal symptoms, perform further medical investigations.\u003cbr\u003e Positive result: near the blue transverse line, a red\/pink one appears near the letter T (Test). This indicates a high probability of the existence of celiac disease. For a final diagnosis, consult your doctor.\u003cbr\u003e Invalid result: if the blue Control line does not appear, the test is to be considered invalid, even if the red\/pink line appears. In this case, it may be that the procedure was not performed correctly, that the reagents have deteriorated, or that an incorrect amount of blood was used. It is therefore necessary to repeat the test.\u003cbr\u003e The test result is valid regardless of the intensity of the color of the lines.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e If the instructions for use are not correctly followed, the test result may be inaccurate. A final diagnosis must be made by a physician, based on clinical symptoms and further supporting laboratory analyses. Before starting a gluten-free diet, consult your doctor. Do not use the test after the expiration date. Do not use the test if the aluminum pouch is damaged. Handle all components with care. The diluent (DIL) contains Proclin 300. It may cause an allergic reaction, do not ingest. All components are single-use. Do not reuse any accessory. Xeliac Test Pro has a sensitivity of 96.5% and a specificity of 97.3%. Alcohol or local anesthetics do not alter the test. The test may give a falsely negative result only in limited cases such as low antibody titers. If the test result is contrary to expectations, consult your doctor. To dispose of used components, place them in the packaging and dispose of them as normal household waste. Keep Xeliac Test Pro out of the reach of children.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eStorage\u003c\/b\u003e\u003cbr\u003e Store all test components at room temperature (+8° + 25° C). The product must be used by the date indicated on the label.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eComponents\u003c\/b\u003e\u003cbr\u003e Aluminum pouch containing: - Finger prick lancet (Dir. 93\/42\/EEC CE0459 Vitrex Medical A\/S, Vasekaer 6-8. 2730 Herlev Denmark)\u003cbr\u003e - Pipette for blood drop collection\u003cbr\u003e - Single-dose diluent\u003cbr\u003e - Plaster (Dir. 93\/42\/EEC - Class 1 - PromoCare B.V. Gerardus Gullaan 14 NL-1217 LN Hilversum - The Netherlands) \u003cbr\u003e \u003cbr\u003e \u003cb\u003eCod.\u003c\/b\u003e 9124\u003c\/div\u003e","brand":"EUROSPITAL SpA","offers":[{"title":"Default Title","offer_id":45942167634187,"sku":"939224150","price":19.69,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_62151d7e-2e59-4333-ae23-11a2c06d5957.jpg?v=1727797966"},{"product_id":"contenitore-per-feci-sterile-prontex-diagnostic-box","title":"STERILE STOOL CONTAINER PRONTEX DIAGNOSTIC BOX","description":"\u003ch1\u003eDiagnostic \u003c\/h1\u003e \u003cb\u003eSTOOL CONTAINER\u003c\/b\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFeatures:\u003c\/b\u003e\u003cbr\u003e sterile container with spatula for coprological analysis. \u003cbr\u003e\u003cbr\u003e \u003cb\u003eCode\u003c\/b\u003e 19180","brand":"SAFETY SpA","offers":[{"title":"Default Title","offer_id":45942218850571,"sku":"908924424","price":1.35,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_63c31b94-4d19-4fb3-bef2-772182b58554.jpg?v=1727798552"},{"product_id":"family-drug-test-5-urine","title":"FAMILY DRUG TEST 5 URINE","description":"\u003ch1\u003e\n\n\u003cfont face=\"Arial\"\u003eFAMILY DRUG\u003c\/font\u003e\u003cbr\u003e \u003cfont face=\"Lucida\" handwriting\u003e\u003ci\u003etest\u003c\/i\u003e\u003c\/font\u003e\n\n\u003c\/h1\u003e \u003cdiv align=\"justify\"\u003e\n\n\u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e Urine drug test, immunoassay, lateral flow, for the qualitative detection of specific drugs and their metabolites in human urine, at the following cut-off concentrations:\u003cbr\u003e\u003cbr\u003e \u003ctable border=\"1cellspacing=0cellpadding=1\" width=\"400\"\u003e \u003ctr align=\"center\"\u003e\n\n\u003ctd\u003eTest\u003c\/td\u003e\n\n\u003ctd\u003eCalibrator\u003c\/td\u003e\n\n\u003ctd\u003eCut-off (ng\/ml)\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eCocaine\u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003eBenzoylecgonine\u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e300\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eMarijuana\u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003eMarijuana\u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e50\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eMethamphetamine\u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003eMethamphetamine\u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e1000\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eOpiates\u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003eMorphine\u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e2000\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eKetamine\u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003eKetamine\u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e1000\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003c\/table\u003e\n\n\u003cbr\u003e The test provides a preliminary result; a more specific alternative chemical method must be used to obtain a confirmatory analytical result. The preferred confirmatory method is Gas Chromatography\/Mass Spectrometry (GC\/MS). Clinical consideration and professional judgment are required for any drug of abuse test result, especially if preliminary results are positive.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eHow to use\u003c\/b\u003e\u003cbr\u003e \u003cu\u003eSpecimen collection and preparation\u003c\/u\u003e\u003cbr\u003e • Wash hands with neutral soap and warm water. Open the sealed package and remove the test.\u003cbr\u003e • Open the container cap and urinate directly into it. The sample volume must exceed the minimum urine level. Cap the container.\u003cbr\u003e \u003cbr\u003e \u003cu\u003ePerforming the test\u003c\/u\u003e\u003cbr\u003e The test must be at room temperature (10°C-30°C).\u003cbr\u003e 1. After urine collection, cap the container and place it on a flat surface.\u003cbr\u003e 2. Lift the label from right to left and read the result within 5 minutes. Do not read results after 5 minutes.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eInterpretation of results\u003c\/u\u003e\u003cbr\u003e \u003cb\u003ePOSITIVE (+)\u003c\/b\u003e A pink band is visible in each control zone. No colored band appears in the appropriate test zone. This indicates a positive result for the drug corresponding to that specific zone.\u003cbr\u003e \u003cb\u003eNEGATIVE (-)\u003c\/b\u003e A pink band is visible in each control zone in the appropriate test zone. This indicates that the concentration of the drug corresponding to that test zone is zero or below the detection limit of the test.\u003cbr\u003e \u003cb\u003eINVALID\u003c\/b\u003e If no colored band is visible in any of the control zones or if it is only visible in the test zones, the test is invalid. Another test must be performed to re-evaluate the sample.\u003cbr\u003e No meaning is attributed to the intensity of the color or the width of the line.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eLimitations\u003c\/u\u003e\u003cbr\u003e 1. This test has been developed exclusively for urine samples. The performance of this test using different samples has not been demonstrated.\u003cbr\u003e 2. Adulterated urine samples may produce erroneous results. Strong oxidizing agents such as bleach (hypochlorite) can oxidize drug analysis. If a sample is suspected of being adulterated, collect a new sample.\u003cbr\u003e 3. This test is a qualitative control. It is not designed to determine the quantitative concentration of drugs or the level of intoxication.\u003cbr\u003e 4. It is possible that technical or procedural errors, as well as other substances that interfere with the urine sample, may cause erroneous results.\u003cbr\u003e 5. A negative result does not necessarily indicate drug-free urine. Negative results can also be obtained when the drug is present but below the test cut-off level.\u003cbr\u003e 6. The test result does not distinguish between drugs of abuse and some medications.\u003cbr\u003e 7. Some foods or supplements may cause positive results.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e This kit is for external use only. Do not swallow.\u003cbr\u003e • Discard after use. The test cannot be used more than once.\u003cbr\u003e • Do not use beyond the expiration date.\u003cbr\u003e • Do not use the kit if the package is punctured or not properly sealed.\u003cbr\u003e • Keep out of reach of children.\u003cbr\u003e • Product not intended for diagnostic medical purposes.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eStorage\u003c\/b\u003e\u003cbr\u003e Store at a temperature of 4°C-30°C until the expiration date. Keep away from light, humidity and heat. Do not freeze.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Package containing: one test, one desiccant, one leaflet.\u003c\/div\u003e","brand":"NOI TEST Srl","offers":[{"title":"Default Title","offer_id":45942265446667,"sku":"921735256","price":16.16,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_97cd3aca-c979-41c6-98af-d09d2e2becee.jpg?v=1727798979"},{"product_id":"contenitore-per-urina-sterile-centrol-baby","title":"STERILE URINE CONTAINER CENTROL BABY","description":"\u003ch1\u003eBaby Centrol\u003c\/h1\u003e \u003cb\u003eSTERILE\u003c\/b\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFeatures:\u003c\/b\u003e\u003cbr\u003e PELD film for pediatric urine collection. \u003cbr\u003eSuitable for both sexes. The contact adhesive is guaranteed to be anti-allergenic.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCode.\u003c\/b\u003e 171","brand":"JONPLAST Srl","offers":[{"title":"Default Title","offer_id":45942362734859,"sku":"908196431","price":1.14,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_bfb48d71-f556-496b-8647-99167865f618.gif?v=1727799767"},{"product_id":"wellion-luna-25-strips-strisce-per-misurazione-glicemia","title":"WELLION LUNA 25 STRIPS GLUCOSE TEST STRIPS","description":"\u003ch2\u003ewellion\u003c\/h2\u003e\u003cdiv align=\"justify\"\u003e \u003ch1\u003eLUNA\u003cbr\u003e 25 GLU\u003c\/h1\u003e \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e Test strips for blood glucose measurement.\u003cbr\u003e Wellion LUNA blood glucose test strips are intended for measuring blood glucose levels in whole blood for self-monitoring with Wellion LUNA series meters at home and in clinical settings by healthcare professionals (in-vitro diagnostics).\u003cbr\u003e Wellion LUNA blood glucose test strips use electrochemical biosensor technology. A whole blood sample is automatically drawn into a reaction zone on the strip by capillary action, resulting in a stable sample volume. When glucose in the whole blood sample reacts with the reagent on the electrodes, Wellion LUNA series meters detect a current when a fixed potential is applied between the electrodes. The current is then converted into a blood glucose concentration reading.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eInstructions for use\u003c\/b\u003e\u003cbr\u003e Sample collection procedures\u003cbr\u003e A fresh capillary blood sample is required for use with Wellion LUNA blood glucose test strips. To ensure accurate results each time you test your blood glucose levels, follow the recommended procedures for obtaining a blood sample:\u003cbr\u003e - clean the chosen test site with warm soapy water, then rinse and dry thoroughly;\u003cbr\u003e - if using an alcohol swab, ensure the puncture site is completely dry before proceeding;\u003cbr\u003e - puncture the chosen site to draw blood. After wiping away the first drop of blood, you can gently massage or rub the area to collect the necessary amount of blood. Do not press excessively on the puncture site;\u003cbr\u003e - to obtain a sufficiently large drop of blood, you can adjust the lancing device to a deeper setting.\u003cbr\u003e \u003cbr\u003e How to perform the test\u003cbr\u003e 1. Remove one strip from the vial and immediately recap it.\u003cbr\u003e 2. Firmly insert the strip into the meter, which will automatically turn on.\u003cbr\u003e 3. Verify that the GLUC test mode symbol is at the top of the meter's LCD screen. If the test mode is not GLUC, insert a new strip.\u003cbr\u003e 4. Use the lancing device to obtain a correctly sized drop of blood. Refer to the user manual or instructions for finger-pricking.\u003cbr\u003e 5. The meter displays the blood drop symbol on the screen; gently touch the blood sample with the tip of the strip. The blood sample will be drawn into the strip's reaction area. When enough blood is present, the countdown will begin after an audible signal from the meter.\u003cbr\u003e 6. Read the test result when the countdown is complete. The result will be stored in the meter's memory.\u003cbr\u003e 7. Remove the strip from the meter, which will automatically turn off. The meter will also automatically turn off after 3 minutes of inactivity.\u003cbr\u003e \u003cbr\u003e Expected results\u003cbr\u003e Wellion LUNA series meters display blood glucose test results from 20 mg\/dL (1.1 mmol\/l) to 600 mg\/dL (33.3 mmol\/l). Expected blood glucose values for people without diabetes:\u003cbr\u003e - generally, the fasting glucose level for a non-diabetic adult is 70-105 mg\/dL (3.9-5.8 mmol\/l) before breakfast and 70-110 mg\/dL (3.9-6.1 mmol\/l) before lunch or dinner;\u003cbr\u003e - one and two hours after meals, normal blood glucose should be between 120-160 mg\/dL (6.7-8.9 mmol\/l) respectively;\u003cbr\u003e - between 2 and 4 AM, blood glucose should be above 70 mg\/dL (3.9 mmol\/l).\u003cbr\u003e \u003cbr\u003e Unexpected or uncertain results\u003cbr\u003e Blood glucose levels that are too low or too high could be symptomatic of serious diseases. If the blood glucose value is unusually high or low or does not reflect your subjective well-being, repeat the test with a new test strip. If the detected value does not conform to your well-being or if the blood glucose result is below 70 mg\/dL (3.9 mmol\/l) or above 180 mg\/dL (10.0 mmol\/l), you should contact your healthcare provider and follow therapeutic suggestions. If test results are unusual or inconsistent, check the following:\u003cbr\u003e - verify that the test strips have not expired;\u003cbr\u003e - check the performance of the meter and test strips by performing a control solution test;\u003cbr\u003e - verify that the blood sample completely fills the test area of the test strip.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e 1. Consult your doctor or healthcare provider before making any therapeutic changes based on test results obtained with the Wellion LUNA series meter.\u003cbr\u003e 2. For using Wellion LUNA blood glucose test strips with Wellion LUNA meters, it is recommended to collect whole blood from the fingertip.\u003cbr\u003e \u003cbr\u003e \u003cb\u003ePrecautions\u003c\/b\u003e\u003cbr\u003e 1. This system is for in-vitro diagnostics only.\u003cbr\u003e 2. Test strips of other brands are not approved for use with Wellion LUNA series meters; using test strips other than Wellion LUNA blood glucose test strips may generate inaccurate results.\u003cbr\u003e 3. Potential biological hazard. Healthcare professionals and others using this system on multiple individuals must be aware that all products or materials exposed to human blood can potentially transmit viral diseases, even after cleaning.\u003cbr\u003e 4. Do not use a Wellion LUNA series meter to perform a test until the control solution test result is within the control range. The system is not working correctly if you continue to get control solution test results outside the range.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eLimitations\u003c\/b\u003e\u003cbr\u003e Observe the following limitations to obtain accurate blood glucose test results with Wellion LUNA series meters and the strip:\u003cbr\u003e - for in-vitro diagnostics only (for external use only);\u003cbr\u003e - do not expose test strips to high humidity or direct sunlight. Do not freeze the strips;\u003cbr\u003e - Wellion blood glucose test strips are for single use only, do not reuse;\u003cbr\u003e - handle the strip with clean, dry hands; thoroughly clean and dry the puncture site for testing;\u003cbr\u003e - do not test with a mobile phone in use nearby; avoid electronic signal interference.;\u003cbr\u003e - high altitude effect: Wellion blood glucose test strips can be used at altitudes up to 3048 m without affecting test results. ;\u003cbr\u003e - hematocrit (Hct) range between 25-60% is acceptable. Hct below 25% may generate elevated results. Hct above 60% may generate reduced blood glucose values compared to the whole blood reference;\u003cbr\u003e - Wellion LUNA blood glucose test strips have not been validated for testing neonatal blood samples. Do not use test strips for testing on neonates;\u003cbr\u003e - the test strips react only with D-glucose and not with other sugars that may be present in the blood.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eComponents\u003c\/b\u003e\u003cbr\u003e Glucose oxidase: \u0026gt;5 units (Aspergillius Niger).\u003cbr\u003e Other components (buffers, mediator, surfactant, stabilizer, etc.): \u0026gt;0.2 mg \u003cb\u003eStorage\u003c\/b\u003e\u003cbr\u003e Store at room temperature between 4-30 °C (39-86 °F). Do not expose directly to sunlight and heat. After removing a strip, immediately close the vial. Use the strip immediately after removing it from the vial. Always store test strips in their original vial. Do not bend, cut, or curve the strips. Handle, remove, touch, and insert the strip gently with clean, dry hands.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCode\u003c\/b\u003e WELL612\u003c\/div\u003e","brand":"MED TRUST ITALIA Srl","offers":[{"title":"Default Title","offer_id":45942415261963,"sku":"926571466","price":10.08,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_d8229e4a-9f39-4b7c-bfe8-077291ba88f2.jpg?v=1727800042"},{"product_id":"test-celiachia-kit-1-pezzo","title":"CELIAC TEST KIT 1 PIECE","description":"\u003ch1\u003eMy\u003cbr\u003eTest\u003c\/h1\u003e \u003cdiv align=\"justify\"\u003e \u003ch2\u003eCeliac Disease\u003c\/h2\u003e \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e Rapid immunochromatographic test for the detection of anti-DGP antibodies of both IgA and IgG classes in whole blood for celiac disease screening.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eInstructions for use\u003c\/b\u003e\u003cbr\u003e 1) Wash hands with warm water and soap, rinse with clean water and dry, or use the provided cleansing wipe. Note: using warm water facilitates capillary blood collection as it induces vasodilation.\u003cbr\u003e 2) Prepare the necessary materials as follows: open the aluminum pouch, take out only the cassette and discard the desiccant sachet. Open the plastic bag containing the pipette. Open the vial by unscrewing the white cap, being careful not to drop it.\u003cbr\u003e 3) Carefully rotate the protective cap of the lancing device 360° without pulling it. Remove and discard the released cap.\u003cbr\u003e 4) Gently massage the chosen finger phalanx for the puncture (the side of the ring finger is recommended). It is important to massage from the palm of the hand towards the phalanx to improve blood flow. Press the lancing device, from the side where the cap was removed, against the fingertip.\u003cbr\u003e The tip of the lancing device automatically retracts safely after use. If the lancing device does not work correctly, use the second one provided. If the latter is not needed, it can be disposed of without special precautions.\u003cbr\u003e 5) Keeping your hand pointing downwards, massage your finger until a large drop of blood forms. It is important to massage from the palm of the hand towards the phalanx to improve blood flow.\u003cbr\u003e 6) Take the pipette without pressing the bulb. Two collection methods are suggested:\u003cbr\u003e – hold the pipette horizontally without pressing the bulb and bring it into contact with the drop of blood; the blood will enter automatically by capillarity. Remove the pipette when it reaches the black line. If there is not enough blood, continue massaging the finger until it reaches that line;\u003cbr\u003e - place the pipette on a clean, flat surface with the tip protruding, then bring the drop of blood into contact with the pipette; the blood will enter automatically by capillarity. Remove the finger when it reaches the black line. If there is not enough blood, continue massaging the finger until it reaches that line. Avoid, as much as possible, interrupting contact between the blood and the pipette to prevent air bubbles from forming.\u003cbr\u003e 7) Take the previously opened vial and immediately deposit the blood collected with the pipette into it. Press the pipette bulb 2 or 3 times and ensure all the blood has gone into the diluent solution. Then reposition the screw cap on the vial and mix well for at least 10 seconds.\u003cbr\u003e 8) Unscrew the blue cap from the dropper bottle (leave the white cap tightly screwed on).\u003cbr\u003e Deposit 3 drops into the well indicated on the cassette.\u003cbr\u003e 9) Wait 10 minutes and interpret the results.\u003cbr\u003e Negative result: only one colored line appears under the C (Control) mark. This result indicates that there are no anti-DGP antibodies in the blood or that their level is below the detectable limit of the test.\u003cbr\u003e Positive result: two colored lines appear in the reading window at the T (Test) and C (Control) marks. The intensity of the T line may be less than the C line. The test should therefore be considered positive regardless of the intensity of the T test band. This result indicates the presence of anti-DGP antibodies in the blood and therefore probable celiac disease. You should consult your doctor to continue the diagnostic process.\u003cbr\u003e Invalid result: no lines appear, or only one line appears under the T (Test) mark and not under the C (Control) mark. In this case, it is not possible to interpret the test result, which must be considered invalid; it is recommended to perform a new test.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e 1) Keep the test out of the reach of children.\u003cbr\u003e 2) Do not use the test after the expiration date shown on the package or if it is damaged.\u003cbr\u003e 3) Follow the procedure exactly, respecting the indicated quantities of blood and diluent.\u003cbr\u003e 4) Do not freeze.\u003cbr\u003e 5) Use the test and the lancing device only once.\u003cbr\u003e 6) The test is for external use only. Do not ingest.\u003cbr\u003e 7) In vitro diagnostic device for individual use.\u003cbr\u003e 8) Not recommended for use by people taking blood-thinning medications (anticoagulants) or people with hemophilia.\u003cbr\u003e 9) After use, dispose of all components according to current local regulations; ask your pharmacist for advice.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eStorage\u003c\/b\u003e\u003cbr\u003e Store the test components at a temperature between +4°C and +30°C.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Hermetically sealed aluminum protective pouch containing: 1 celiac test device and 1 desiccant sachet; 2 sterile lancing devices for self-puncture for blood collection; 1 dropper bottle containing enough celiac test diluent for 1 test; 1 plastic bag containing 1 pipette for blood collection; 1 antiseptic cleansing wipe for the skin and 1 instruction leaflet. \u003c\/div\u003e","brand":"COOPER CONSUMER HEALTH IT Srl","offers":[{"title":"Default Title","offer_id":45942417162507,"sku":"942423688","price":4.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_a03bd399-7eb0-41ae-bd14-2c2e4cfbcc98.jpg?v=1727800058"},{"product_id":"contenitore-per-urina-da-2500-ml-pharmamentis-con-tappo-a-vite-24-h","title":"2500 ML PHARMAMENTIS URINE CONTAINER WITH 24 H SCREW CAP","description":"\u003ch3\u003ePharmamentis\u003c\/h3\u003e\u003cdiv align=\"justify\"\u003e \u003ch1\u003eURINE CONTAINER\u003c\/h1\u003e \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e 24-hour urine collection container.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eStorage\u003c\/b\u003e\u003cbr\u003e Store at room temperature in a dry place, away from heat sources.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e 2,500 ml urine container. \u003c\/div\u003e","brand":"V.I.M. Srl","offers":[{"title":"Default Title","offer_id":45942502621451,"sku":"987741954","price":4.25,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_01365e21-c09b-4a96-8b5c-e5afb4133f7c.jpg?v=1727800952"},{"product_id":"screen-droga-test-10-droghe-test-antidroga-con-contenitore-urina","title":"SCREEN DRUG TEST 10 DRUGS DRUG TEST WITH URINE CUP","description":"\u003ch2\u003e\n\n\u003ci\u003eSCREEN\u003c\/i\u003e\u003cbr\u003e DRUG TEST\u003cbr\u003e \u003cbr\u003e URINE 10\u003c\/h2\u003e \u003cdiv align=\"justify\"\u003eInstructions for use for each test combination of the following drugs: methamphetamine, methadone, amphetamine, barbiturates, tricyclic antidepressants, phencyclidine, cocaine, marijuana, opiates, benzodiazepines.\u003cbr\u003e One-step test for the simultaneous qualitative determination of drugs and their metabolites in human urine.\u003cbr\u003e \u003cbr\u003e \u003cb\u003ePrecautions\u003c\/b\u003e\u003cbr\u003e • Product not intended for medical or diagnostic use.\u003cbr\u003e • Do not use beyond the expiration date.\u003cbr\u003e • Store the test strip panel in the sealed pouch until use.\u003cbr\u003e • All samples must be considered potentially hazardous and, therefore, must be handled with precautions related to potentially infectious products.\u003cbr\u003e • After use, the panel must be disposed of according to local regulations in force.\u003cbr\u003e Store in the sealed pouch at a temperature between 2° and 30°C.\u003cbr\u003e The test strip panel is stable until the expiration date indicated on the pouch label.\u003cbr\u003e The test strip panel must be stored in the sealed pouch until use.\u003cbr\u003e Do not freeze.\u003cbr\u003e Do not use beyond the expiration date.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eIntended Use and Summary\u003c\/b\u003e\u003cbr\u003e Screening test for the simultaneous determination of various drugs.\u003cbr\u003e The speed and sensitivity of immunoassay tests have led them to be considered the most accepted as screening tests in urine for the simultaneous detection of drugs of abuse.\u003cbr\u003e The one-step test strip panel (Urine) is a rapid lateral flow immunochromatographic test for the qualitative determination of the following drugs without the aid of instruments:\u003cbr\u003e \u003ctable border=\"1cellspacing=0cellpadding=1\" width=\"400\"\u003e \u003ctr\u003e\n\n\u003ctd\u003e\u003cb\u003eTest\u003c\/b\u003e\u003c\/td\u003e\n\n\u003ctd\u003e\u003cb\u003eCalibrator\u003c\/b\u003e\u003c\/td\u003e\n\n\u003ctd\u003e\u003cb\u003eCut-off (ng\/ml)\u003c\/b\u003e\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eMethamphetamine (MET\/MDMA)\u003c\/td\u003e\n\n\u003ctd\u003eD-Methamphetamine\u003c\/td\u003e\n\n\u003ctd\u003e 1,000\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eMethadone (MTD)\u003c\/td\u003e\n\n\u003ctd\u003e Methadone\u003c\/td\u003e\n\n\u003ctd\u003e 300\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eAmphetamine (AMP)\u003c\/td\u003e\n\n\u003ctd\u003e D-Amphetamine \u003c\/td\u003e\n\n\u003ctd\u003e1,000\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eBarbiturates (BAR)\u003c\/td\u003e\n\n\u003ctd\u003e Secobarbital \u003c\/td\u003e\n\n\u003ctd\u003e300\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eTricyclic Antidepressants (TCA)\u003c\/td\u003e\n\n\u003ctd\u003e Nortriptyline\u003c\/td\u003e\n\n\u003ctd\u003e 1,000\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003ePhencyclidine (PCP) \u003c\/td\u003e\n\n\u003ctd\u003ePhencyclidine \u003c\/td\u003e\n\n\u003ctd\u003e25\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eCocaine (COC) \u003c\/td\u003e\n\n\u003ctd\u003eBenzoylecgonine \u003c\/td\u003e\n\n\u003ctd\u003e300\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eMarijuana (THC) \u003c\/td\u003e\n\n\u003ctd\u003e11-nor-Δ9 -THC-9 COOH \u003c\/td\u003e\n\n\u003ctd\u003e50\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eOpiates (OPI)\u003c\/td\u003e\n\n\u003ctd\u003e Morphine\u003c\/td\u003e\n\n\u003ctd\u003e 2,000\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eBenzodiazepines (BZO) \u003c\/td\u003e\n\n\u003ctd\u003eOxazepam \u003c\/td\u003e\n\n\u003ctd\u003e300\u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\n\u003c\/table\u003e\n\n\u003cbr\u003e This test provides only preliminary analytical data.\u003cbr\u003e More specific chemical methods must be used to confirm the analytical result.\u003cbr\u003e Gas chromatography and mass spectrometry (GC\/MS) are considered preferential confirmatory methods.\u003cbr\u003e Any result for the determination of the presence of drugs of abuse must be correlated with clinical considerations and professional judgment, particularly when the preliminary result is positive.\u003cbr\u003e \u003cbr\u003e Rapid urine screening test that does not require the use of special instruments.\u003cbr\u003e The test uses antibodies to selectively detect high levels of specific substances in human urine.\u003cbr\u003e The residence times are approximate for each substance as they vary depending on frequency of use, body mass, age, health status, drug tolerance, and urine pH.\u003cbr\u003e The product detects the presence of narcotic substances in urine only after their metabolization.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCOCAINE (COC)\u003c\/b\u003e\u003cbr\u003e Cocaine is a potent central nervous system stimulant as well as a local anesthetic derived from the coca plant.\u003cbr\u003e The substance is often self-administered via inhalation or intravenous injection or by smoking the base substance.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eAMPHETAMINE (AMP)\u003c\/b\u003e\u003cbr\u003e Amphetamine is a substance also used for therapeutic purposes.\u003cbr\u003e The substance is often self-administered via inhalation or ingestion.\u003cbr\u003e High doses produce enhanced central nervous system stimulation and induce euphoria, alertness, appetite suppression, increased energy and strength.\u003cbr\u003e More acute reactions produce anxiety, paranoia, hallucinations and psychotic behavior.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eMETHAMPHETAMINE (MET\/MDMA)\u003c\/b\u003e\u003cbr\u003e Methamphetamine is a potent stimulant chemically related to amphetamine, but with a greater capacity for central nervous system stimulation.\u003cbr\u003e The substance is often self-administered via inhalation, smoking, or ingestion.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eMARIJUANA (THC)\u003c\/b\u003e\u003cbr\u003e Tetrahydrocannabinol is the active ingredient in cannabis.\u003cbr\u003e When smoked or taken orally, THC produces euphoria.\u003cbr\u003e Regular users experience short-term memory impairment and learning delays, and may also have transient episodes of confusion and anxiety.\u003cbr\u003e Relatively heavy long-term use may be associated with behavioral disorders.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eOPIATES (OPI)\u003c\/b\u003e\u003cbr\u003e The opiate class refers to any substance derived from the opium poppy, including natural compounds such as morphine, codeine, and semi-synthetic substances such as heroin.\u003cbr\u003e Opiates act on pain control by depressing the central nervous system.\u003cbr\u003e Withdrawal symptoms may include sweating, tremors, nausea, and irritability.\u003cbr\u003e Opiates can be taken orally or by intravenous, intramuscular, and subcutaneous injection.\u003cbr\u003e Users can also take the substance intravenously or by inhalation.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eMETHADONE (MTD)\u003c\/b\u003e\u003cbr\u003e Methadone is a narcotic analgesic prescribed for the treatment of severe to moderate pain and for the treatment of opiate addiction (heroin, Vicodin, Percocet, Morphine).\u003cbr\u003e Methadone is a long-acting analgesic that produces effects lasting from twelve to forty-eight hours.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eBARBITURATES (BAR)\u003c\/b\u003e\u003cbr\u003e Barbiturates are used in medicine as sedatives, hypnotics, and anticonvulsants.\u003cbr\u003e Barbiturates are almost always taken orally in the form of capsules or tablets.\u003cbr\u003e The effects resemble those of alcohol intoxication.\u003cbr\u003e Chronic use of Barbiturates leads to tolerance and physical dependence.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eBENZODIAZEPINES (BZO)\u003c\/b\u003e\u003cbr\u003e Benzodiazepines are frequently prescribed medications for the symptomatic treatment of anxiety and sleep disorders.\u003cbr\u003e They produce their effects through specific receptors involving a neurochemical called gamma-aminobutyric acid (GABA).\u003cbr\u003e Due to their greater safety and efficacy, benzodiazepines have replaced barbiturates in the treatment of anxiety and insomnia.\u003cbr\u003e Benzodiazepines are also used as sedatives before surgical and medical procedures and for the treatment of epileptic seizures and alcohol withdrawal.\u003cbr\u003e \u003cbr\u003e \u003cb\u003ePHENCYCLIDINE (PCP)\u003c\/b\u003e\u003cbr\u003e Phencyclidine, also known as PCP or Angel Dust, is a hallucinogen used in powder, capsule, and tablet form.\u003cbr\u003e The powder is inhaled or smoked after being mixed with marijuana or plant substances.\u003cbr\u003e PCP is commonly administered by inhalation but can also be used intravenously, intranasally, and orally.\u003cbr\u003e Following small doses, users think and act quickly and experience mood alterations from euphoria to depression.\u003cbr\u003e Self-destructive behavior is one of the effects of PCP.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eTRICYCLIC ANTIDEPRESSANTS (TCA)\u003c\/b\u003e\u003cbr\u003e TCAs (tricyclic antidepressants) are commonly used for the treatment of depressive disorders.\u003cbr\u003e TCA overdoses can cause profound depression, cardiotoxicity, and anticholinergic effects.\u003cbr\u003e TCA overdose is the leading cause of drug-related death.\u003cbr\u003e TCAs are taken orally or sometimes by injection.\u003cbr\u003e \u003cbr\u003e \u003cb\u003ePRINCIPLE\u003c\/b\u003e\u003cbr\u003e The one-step test strip panel (Urine) is a rapid immunochromatographic test based on the principle of competitive binding.\u003cbr\u003e Drugs that may be present in the urine sample compete with the corresponding conjugate for the same antibody binding sites.\u003cbr\u003e During the test, a urine sample migrates by capillarity along the membrane.\u003cbr\u003e If a drug is present in the urine sample at a concentration below its cut-off, it will not be able to saturate all the binding sites of the antibody-bound particles present in the strip.\u003cbr\u003e The antibody-bound particles will be captured by the immobilized conjugate, and a visible colored band will appear in the test band region of the corresponding strip.\u003cbr\u003e The colored band will not form in the corresponding area if the drug level is above its cut-off, as all binding sites of the corresponding antibodies will be saturated.\u003cbr\u003e A urine sample positive for the drug being tested will not cause the formation of the colored band due to drug competition, while a urine sample negative for the drug being tested or a sample containing a drug concentration below the cut-off will cause the formation of the colored band in the specific test area.\u003cbr\u003e As a procedural control, a colored band will appear in the control area, indicating that a correct amount of sample has been used and that membrane migration has occurred.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eREAGENTS\u003c\/b\u003e\u003cbr\u003e Each strip of the panel contains mouse monoclonal antibodies bound to particles and the corresponding.\u003cbr\u003e The one-step test strip panel (Urine) is a rapid lateral flow immunochromatographic test conjugated for each drug.\u003cbr\u003e Goat antibodies are used for the control band.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eSAMPLE COLLECTION AND PREPARATION\u003c\/b\u003e\u003cbr\u003e Collect the urine sample in a clean and dry container.\u003cbr\u003e Urine samples collected at any time of the day can be used.\u003cbr\u003e Urine samples with obvious precipitate must be centrifuged, filtered, or allowed to settle to obtain a clear sample for testing.\u003cbr\u003e Urine samples can be stored at 2-8°C for a maximum of 48 hours.\u003cbr\u003e For prolonged storage, samples can be frozen and stored at temperatures below -20°C.\u003cbr\u003e Before using frozen samples, they must be thawed and thoroughly homogenized.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eOPERATING PROCEDURE\u003c\/b\u003e\u003cbr\u003e 1. Before opening the pouch, bring it to room temperature.\u003cbr\u003e Remove the product from the pouch and use it as soon as possible.\u003cbr\u003e 2. Remove the cap from the strips.\u003cbr\u003e Immerse the product vertically, in the direction of the arrows, into the urine sample for at least 10\/15 seconds. Immerse the product up to the level of the wavy lines on the strips but not above them.\u003cbr\u003e 3. Replace the cap on the device and place the product horizontally on a flat, non-absorbent surface.\u003cbr\u003e Read the result after 5 minutes.\u003cbr\u003e Do not interpret the result after 10 minutes.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eINTERPRETATION OF RESULTS\u003c\/b\u003e\u003cbr\u003e Negative*: a colored band appears in the control region (C) and a second in the test region (T) for each drug, indicating a negative result.\u003cbr\u003e A negative result indicates that the concentration of the drug in question in the urine is below the detectable cut-off level for that specific drug.\u003cbr\u003e \u003cfont size=\"2\"\u003e*the shade of color in the test region (T) may vary, but any faint colored band should be considered negative.\u003c\/font\u003e\u003cbr\u003e Positive: a colored band appears in the control region (C) but not in the test region (T) for each drug, indicating a positive result.\u003cbr\u003e A positive result indicates that the concentration of the drug in question in the urine is above the detectable cut-off level for that specific drug.\u003cbr\u003e Invalid: no control band (C) appears.\u003cbr\u003e The most plausible causes for the absence of the control band may be insufficient sample volume or an incorrect analytical procedure.\u003cbr\u003e Recheck the procedure and repeat the test using a new panel.\u003cbr\u003e If the problem persists, immediately discontinue use of the kit and contact your local distributor.\u003cbr\u003e If the test result is positive, avoid aggressive behavior and calmly seek dialogue with the person concerned.\u003cbr\u003e Consult your doctor, a psychologist, or contact the relevant service in your area.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eQUALITY CONTROL\u003c\/b\u003e\u003cbr\u003e The test includes an internal control system consisting of the red band that appears in the control region (C).\u003cbr\u003e The appearance of this band confirms that the test has been performed correctly with sufficient sample volume, that membrane absorption was adequate, and the procedure was correct.\u003cbr\u003e Standard controls are not provided with the kit; however, it is recommended to test positive and negative controls, as good laboratory practice, to confirm the test procedure and verify its correct characteristics.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eLIMITATIONS\u003c\/b\u003e\u003cbr\u003e The test includes an internal control system consisting of the red band that appears in the control region (C).\u003cbr\u003e The appearance of this band confirms that the test has been performed correctly with sufficient sample volume, that membrane absorption was adequate, and the procedure was correct.\u003cbr\u003e Standard controls are not provided with the kit; however, it is recommended to test positive and negative controls, as good laboratory practice, to confirm the test procedure and verify its correct characteristics.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFORMAT\u003c\/b\u003e\u003cbr\u003e Kit containing:\u003cbr\u003e • 1 urine container.\u003cbr\u003e • 1 Urine Drug Test 10.\u003cbr\u003e • 1 instruction leaflet.\u003c\/div\u003e","brand":"SCREEN ITALIA Srl","offers":[{"title":"Default Title","offer_id":45942816243979,"sku":"927972327","price":18.33,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_8d389549-fbbd-4732-85c2-be9b3edce25c.jpg?v=1727804304"},{"product_id":"test-colesterolo-totale-accutrend-cholesterol-5-pezzi","title":"ACCUTREND CHOLESTEROL TOTAL CHOLESTEROL TEST 5 PIECES","description":"\u003ch1\u003eAccutrend Cholesterol\u003c\/h1\u003e \u003cb\u003eTEST STRIPS\u003c\/b\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eIndications:\u003c\/b\u003e\u003cbr\u003e for home self-monitoring of total cholesterol.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFeatures:\u003c\/b\u003e\u003cbr\u003e allows determination of total cholesterol in capillary blood in the range of 150-300 mg\/dl.\u003cbr\u003e The use of this strip, which works exclusively with the Accutrend GC device, is particularly useful for screening and preventing dysmetabolic diseases, to identify patients who unknowingly suffer from lipid metabolism disorders.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCode\u003c\/b\u003e 1418262 \/ 1418254","brand":"ROCHE DIAGNOSTICS SpA","offers":[{"title":"Default Title","offer_id":45942828761355,"sku":"907027383","price":34.4,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_925e7c15-ce70-476e-8aff-24ac9f4e8d57.jpg?v=1727804577"},{"product_id":"contenitore-per-feci-da-60ml-pharmamentis-con-tappo-a-vite","title":"60ml Stool Container PHARMAMENTIS with Screw Cap","description":"\u003ch1\u003eSTOOL CONTAINER\u003c\/h1\u003e \u003cdiv align=\"justify\"\u003e \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e Class A in vitro diagnostic medical device.\u003cbr\u003e Stool container with red screw cap. Intended exclusively for the collection and transport of biological samples for laboratory analysis, in the case of stool tests.\u003cbr\u003e Beta-ray sterile.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eComponents\u003c\/b\u003e\u003cbr\u003e Container: polypropylene.\u003cbr\u003e Cap: polyethylene.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e Do not place in contact with or near flames.\u003cbr\u003e Do not discard the product in the environment as it is not biodegradable.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eStorage\u003c\/b\u003e\u003cbr\u003e Store at room temperature in a dry place, away from heat sources.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Capacity: 60 ml\u003c\/div\u003e","brand":"V.I.M. Srl","offers":[{"title":"Default Title","offer_id":45942873948427,"sku":"985725985","price":0.75,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_f8779def-f6f4-4d8a-9f3d-5689aa066da9.jpg?v=1727805608"},{"product_id":"screen-droga-test-marijuana-test-antidroga-con-contenitore-urina","title":"SCREEN DRUG TEST MARIJUANA DRUG TEST WITH URINE CONTAINER","description":"927922\u003ch2\u003e\n\n\u003ci\u003eSCREEN\u003c\/i\u003e\u003cbr\u003e DRUG TEST\u003cbr\u003e \u003cbr\u003e Marijuana\u003c\/h2\u003e \u003cdiv align=\"justify\"\u003eInstructions for use for each test combination of the following drugs: amphetamine, benzodiazepine, cocaine, marijuana, methylenedioxymethamphetamine, ketamine, opiates, synthetic marijuana k2\/spice.\u003cbr\u003e Single-phase test for the simultaneous qualitative determination of drugs and their metabolites in human urine.\u003cbr\u003e \u003cbr\u003e \u003cb\u003ePrecautions\u003c\/b\u003e\u003cbr\u003e Product not intended for medical or diagnostic use.\u003cbr\u003e Do not use beyond the expiry date.\u003cbr\u003e Store the test strip panel in the sealed pouch until use.\u003cbr\u003e All samples must be considered potentially hazardous and, therefore, handled with the precautions for use related to potentially infectious products.\u003cbr\u003e After use, the panel must be disposed of according to local regulations in force.\u003cbr\u003e Store in the sealed pouch at a temperature between 2° and 30°C.\u003cbr\u003e The test strip panel is stable until the expiry date indicated on the pouch label.\u003cbr\u003e The test strip panel must be stored in the sealed pouch until use.\u003cbr\u003e Do not freeze.\u003cbr\u003e Do not use beyond the expiry date.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eIntended use and summary\u003c\/b\u003e\u003cbr\u003e Screening test for the simultaneous determination of various drugs.\u003cbr\u003e The speed and sensitivity of immunoassays have led them to be considered the most accepted as screening tests in urine for the simultaneous detection of drugs of abuse.\u003cbr\u003e The single-phase test strip panel (Urine) is a rapid lateral flow immunochromatographic test for the qualitative determination of the following drugs without the aid of instruments:\u003cbr\u003e \u003ctable border=\"1cellspacing=0cellpadding=1\" width=\"600\"\u003e \u003ctr align=\"center\"\u003e\n\n\u003ctd\u003e\u003cb\u003eTest\u003c\/b\u003e\u003c\/td\u003e\n\n\u003ctd\u003e\u003cb\u003eCalibrator\u003c\/b\u003e\u003c\/td\u003e \u003ctd\u003e\u003cb\u003eCut-off (ng\/ml)\u003c\/b\u003e\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eCocaine (COC)\u003cbr\u003e Amphetamine (AMP)\u003cbr\u003e Methylenedioxymethamphetamine (MDMA)\u003cbr\u003e Marijuana (THC)\u003cbr\u003e Opiates (OPI)\u003cbr\u003e Benzodiazepine (BZO)\u003cbr\u003e Ketamine (KET)\u003cbr\u003e Synthetic marijuana k2\/spice\u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003ebenzoylecgonine\u003cbr\u003e D-amphetamine\u003cbr\u003e D,L-methylenedioxymethamphetamine\u003cbr\u003e 11-nor-Δ\u003csup\u003e9\u003c\/sup\u003e-THC-9 COOH\u003cbr\u003e morphine\u003cbr\u003e Oxazepam\u003cbr\u003e Ketamine\u003cbr\u003e jwh-018 and jwh-073\u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e300\u003cbr\u003e 1,000\u003cbr\u003e 500\u003cbr\u003e 50\u003cbr\u003e 2,000\u003cbr\u003e 300\u003cbr\u003e 1,000\u003cbr\u003e 50\u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\n\u003c\/table\u003e \u003cbr\u003e This test only provides preliminary analytical data.\u003cbr\u003e More specific chemical methods must be used to confirm the analytical result.\u003cbr\u003e Gas chromatography and mass spectrometry (GC\/MS) are considered preferred confirmatory methods.\u003cbr\u003e Any result for the determination of the presence of drugs of abuse must be correlated with clinical considerations and professional judgment, particularly when the preliminary result is positive.\u003cbr\u003e It is a rapid urine screening test that does not require the use of special instruments.\u003cbr\u003e The test uses antibodies to selectively detect high levels of specific substances in human urine.\u003cbr\u003e \u003cbr\u003e The residence times are approximate for each substance as they vary based on frequency of use, body mass, age, health status, tolerance to narcotic substances and urine pH.\u003cbr\u003e The product detects the presence of narcotic substances in urine only after their metabolization.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eCOCAINE (COC)\u003c\/u\u003e\u003cbr\u003e Cocaine is a powerful central nervous system stimulant as well as a local anesthetic derived from the coca plant.\u003cbr\u003e The substance is often self-administered by inhalation or intravenous injection or by smoking the base substance.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eAMPHETAMINE (AMP)\u003c\/u\u003e\u003cbr\u003e Amphetamine is a substance also used for therapeutic purposes.\u003cbr\u003e The substance is often self-administered by inhalation or ingestion.\u003cbr\u003e High doses produce enhanced central nervous system stimulation and induce euphoria, alertness, appetite reduction, a sense of increased energy and strength.\u003cbr\u003e More acute reactions produce anxiety, paranoia, hallucinations and psychotic behavior.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eMETHYLENEDIOXYMETHAMPHETAMINE (MDMA)\u003c\/u\u003e\u003cbr\u003e Ecstasy is not a stimulant, although it shares with amphetamines the ability to increase blood pressure and heart rate.\u003cbr\u003e It produces some changes in perception such as increased sensitivity to light, difficulty focusing, blurred vision.\u003cbr\u003e The effect that occurs in practically everyone who takes this substance is to clench their jaw.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eMARIJUANA (THC)\u003c\/u\u003e\u003cbr\u003e Tetrahydrocannabinol is the active ingredient in cannabis.\u003cbr\u003e When smoked or taken orally, THC produces euphoria.\u003cbr\u003e Regular users have short-term memory impairment and delayed learning; they may also have transient episodes of confusion and anxiety.\u003cbr\u003e Relatively heavy long-term use may be associated with behavioral disorders.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eOPIATES (OPI)\u003c\/u\u003e\u003cbr\u003e The class of opiates refers to any substance derived from the opium poppy, including natural compounds such as morphine, codeine and semi-synthetic substances such as heroin.\u003cbr\u003e Opiates act on pain control by depressing the central nervous system.\u003cbr\u003e Withdrawal symptoms may include sweating, tremors, nausea and irritability.\u003cbr\u003e Opiates can be taken orally or by intravenous, intramuscular and subcutaneous injection.\u003cbr\u003e Users can also take the substance intravenously or by inhalation.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eBENZODIAZEPINE (BZO)\u003c\/u\u003e\u003cbr\u003e These are frequently prescribed drugs for the symptomatic treatment of anxiety, sleep disorders, epileptic seizures and alcohol withdrawal syndrome.\u003cbr\u003e Abrupt discontinuation can induce symptoms such as sleep disorders, gastrointestinal problems, loss of appetite, sweating, tremor, weakness, anxiety and changes in perception.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eKETAMINE (KET)\u003c\/u\u003e\u003cbr\u003e Ketamine is a dissociative anesthetic for human and veterinary use.\u003cbr\u003e It is marketed in Italy under the names Ketalar, Ketanest and Ketaset and in humans it is classified as a Class H drug and should only be used in a hospital setting by an anesthetist-resuscitator.\u003cbr\u003e Like all neuro-psychotropic drugs, it can be abused and used voluntarily, which is forbidden and sanctioned by law, as a narcotic substance.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eSYNTHETIC MARIJUANA K2\/SPICE (K2\/SPICE)\u003c\/u\u003e\u003cbr\u003e Synthetic Marijuana or K2 is a psychoactive herb and chemical product that, when consumed, mimics the effects of Marijuana.\u003cbr\u003e Most commonly known by the trade names K2 and Spice, both widely used to refer to any synthetic Marijuana product.\u003cbr\u003e \u003cbr\u003e \u003cb\u003ePrinciple\u003c\/b\u003e\u003cbr\u003e The single-phase test strip panel (Urine) is a rapid immunochromatographic test based on the principle of competitive binding.\u003cbr\u003e Drugs that may be present in the urine sample compete with the relevant conjugate for the same antibody binding sites.\u003cbr\u003e During the test, a urine sample migrates by capillarity along the membrane.\u003cbr\u003e A drug, if present in the urine sample, at a concentration lower than its cut-off, will not be able to saturate all the binding sites of the antibody-bound particles present in the strip.\u003cbr\u003e The antibody-bound particles will be captured by the immobilized conjugate and a visible colored band will appear in the test band area of the relevant strip.\u003cbr\u003e The colored band will not form in the relevant area if the drug level is higher than its cut-off, as all the binding sites of the relevant antibodies will be saturated.\u003cbr\u003e A urine sample positive for the drug under examination will not cause the formation of the colored band due to drug competition, while a urine sample negative for the drug under examination or a sample containing a drug concentration below the cut-off will cause the formation of the colored band in the specific test area.\u003cbr\u003e As a procedural control, a colored band will appear in the relevant area, indicating that a correct amount of sample has been used and that migration on the membrane has occurred.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eReagents\u003c\/b\u003e\u003cbr\u003e Each strip of the panel contains mouse monoclonal antibodies bound to particles and the corresponding.\u003cbr\u003e The single-phase test strip panel (Urine) is a rapid lateral flow immunochromatographic test conjugated for each drug.\u003cbr\u003e Goat antibodies are used for the control band.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eSample collection and preparation\u003c\/b\u003e\u003cbr\u003e Collect the urine sample in a clean and dry container.\u003cbr\u003e Urine samples collected at any time of day can be used.\u003cbr\u003e Urine samples with obvious presence of precipitate must be centrifuged, filtered or allowed to settle to obtain a clear sample on which to perform the test.\u003cbr\u003e Urine samples can be stored at a temperature of 2-8°C for a maximum of 48 hours.\u003cbr\u003e For prolonged storage, samples can be frozen and stored at a temperature below -20°C.\u003cbr\u003e Before using frozen samples, they must be thawed and thoroughly homogenized.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eInstructions for use\u003c\/b\u003e\u003cbr\u003e 1. Before opening the pouch, bring it to room temperature. Remove the product from the pouch and use it as soon as possible.\u003cbr\u003e 2. Remove the cap from the strips. Immerse the product vertically, in the direction of the arrows, into the urine sample for at least 10\/15 seconds. Immerse the product up to the level of the wavy lines on the strips but not above them.\u003cbr\u003e 3. Replace the cap on the device and place the product horizontally on a flat, non-absorbent surface. Read the result after 5 minutes. Do not interpret the result after 10 minutes.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eInterpretation of results\u003c\/b\u003e\u003cbr\u003e \u003cu\u003eNegative*:\u003c\/u\u003e a colored band appears in the control region (C) and a second in the test region (T) for each drug, indicating a negative result.\u003cbr\u003e A negative result indicates that the concentration of the drug in question in the urine is below the detectable cut-off level for that specific drug.\u003cbr\u003e \u003cfont size=\"2\"\u003e*the shade of color in the test region (T) may vary, but any faint colored band should be considered negative.\u003c\/font\u003e\u003cbr\u003e \u003cu\u003ePositive:\u003c\/u\u003e a colored band appears in the control region (C) but not in the test region (T) for each drug, indicating a positive result.\u003cbr\u003e A positive result indicates that the concentration of the drug in question in the urine is above the detectable cut-off level for that specific drug.\u003cbr\u003e \u003cu\u003eInvalid:\u003c\/u\u003e no control band (C) appears.\u003cbr\u003e The most plausible causes for the absence of the control band may be insufficient sample volume or incorrect analytical procedure.\u003cbr\u003e Recheck the procedure and repeat the test using a new panel.\u003cbr\u003e If the problem persists, immediately stop using the kit and contact your local distributor.\u003cbr\u003e If the test result is positive, avoid aggressive behavior and calmly seek dialogue with the person concerned.\u003cbr\u003e Seek advice from your doctor, a psychologist or contact the relevant service in your area.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eQuality control\u003c\/b\u003e\u003cbr\u003e The test includes an internal control system consisting of the red band that appears in the control region (C).\u003cbr\u003e The appearance of this band confirms that the test has been performed correctly with sufficient sample volume, that the membrane absorption was adequate and the procedure correct.\u003cbr\u003e Standard controls are not supplied with the kit; however, it is recommended to test positive and negative controls, as good laboratory practice, to confirm the test procedure and verify its correct characteristics.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eLimitations\u003c\/b\u003e\u003cbr\u003e 1. The single-phase test strip panel (Urine) provides only a preliminary qualitative analytical result. A second analytical method must be adopted. Gas chromatography and mass spectrometry (GC\/MS) are considered preferred confirmatory methods if the test result is positive.\u003cbr\u003e 2. It is possible that technical or procedural errors, as well as interfering substances present in the urine sample, may cause erroneous results.\u003cbr\u003e 3. It is possible that adulterating substances, such as bleach and\/or alum present in the urine sample, may cause erroneous results regardless of the analytical method used. If the presence of such substances is suspected, the test must be repeated with another urine sample.\u003cbr\u003e 4. A positive result indicates the presence of the drug or its metabolites but not the level of intoxication, the route of administration or the concentration in the urine.\u003cbr\u003e 5. A negative result does not necessarily mean that the urine sample is drug-free. A negative result can be obtained when the drug is present but at a concentration below the test's cut-off level.\u003cbr\u003e 6. The test cannot distinguish between the drug and a medicine containing the same substance; false positives can be caused by some drugs.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e • 1 urine container.\u003cbr\u003e • 1 Cocaine Drug Test.\u003cbr\u003e • instruction leaflet.\u003c\/div\u003e","brand":"SCREEN ITALIA Srl","offers":[{"title":"Default Title","offer_id":45942875029771,"sku":"911151696","price":8.11,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_397c1fd6-61f9-4144-8103-b0a80c790512.jpg?v=1727805635"},{"product_id":"screen-test-rapido-fsh-menopausa-urina-2-pezzi","title":"FSH\/MENOPAUSE RAPID URINE SCREEN TEST 2 PIECES","description":"\u003ch1\u003eSCREEN\u003cbr\u003e CHECK TEST\u003c\/h1\u003e \u003cb\u003eMenopause\u003c\/b\u003e\u003cbr\u003e \u003cbr\u003e \u003cdiv align=\"justify\"\u003e\n\n\u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e Rapid flow test for the qualitative detection of Follicle-Stimulating Hormone (FSH) in urine samples.\u003cbr\u003e For in vitro self-diagnostic use only.\u003cbr\u003e \u003cbr\u003e \u003cb\u003ePrecautions\u003c\/b\u003e\u003cbr\u003e - Do not use beyond the expiry date printed on the sealed packaging.\u003cbr\u003e - The test must remain in its sealed packaging until use.\u003cbr\u003e - Store in a dry place at 2-30°C or 36-86°F. Do not freeze.\u003cbr\u003e - Do not use if the packaging is torn or damaged.\u003cbr\u003e - For in vitro diagnostic use only.\u003cbr\u003e - Keep out of reach of children.\u003cbr\u003e - Do not open the test packaging until you are ready to start the test.\u003cbr\u003e - Use only once.\u003cbr\u003e - The used test must be disposed of according to local regulations.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eWhen to perform the test\u003c\/b\u003e\u003cbr\u003e If you still have your period every month, perform the first test during the first week of your cycle (days 2-7, considering day 1 as the first day of menstruation). If the result is negative but symptoms persist, repeat the test one week later.\u003cbr\u003e If you no longer have regular periods, perform the test at any time of the month and repeat it 1 week later.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eHow to use\u003c\/b\u003e\u003cbr\u003e Bring the test, urine sample, and\/or controls to room temperature (15-30°C) before testing.\u003cbr\u003e 1. Determine the day to perform the test.\u003cbr\u003e 2. Bring the packaging to room temperature before opening. Remove the test device from the sealed packaging and use it immediately within one hour.\u003cbr\u003e 3. Remove the cap from the device and hold the test so that the absorbent tip is placed in the urine stream or place the absorbent tip (=2\/3) in the urine sample in a clean container for at least 10-15 seconds.\u003cbr\u003e 4. Replace the cap on the test, then place it on a clean, stable surface with the test and control windows facing upwards, then immediately start the timer.\u003cbr\u003e 5. When the test starts to work, you may notice a slight color flowing through the results window.\u003cbr\u003e Read the results after 3 minutes. If no result appears, wait another minute. Do not read the results after 10 minutes.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eReading the results\u003c\/b\u003e\u003cbr\u003e POSITIVE: two visible lines appear and the one in the test region (T) is of equal or greater intensity than the one in the control region (C). A positive result indicates that the FSH level is higher than normal. Record the results and compare them with the table to interpret the results.\u003cbr\u003e NEGATIVE: two lines are visible, but the one in the test region (T) is lighter than the one in the control region (C) or there is no line in the test region (T). A negative result indicates that the FSH level is not elevated. Record the results and compare them with the table to interpret the results.\u003cbr\u003e INVALID: no control line appears. The most probable causes for the absence of the control line are insufficient volume or incorrect procedural techniques. Review the procedure and repeat the test with a new device. If the problem persists, stop using the kit immediately and contact your local distributor.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eTest interpretation\u003c\/b\u003e\u003cbr\u003e For women experiencing pre-menopause symptoms combined with irregular menstrual cycles:\u003cbr\u003e \u003ctable border=\"1cellspacing=0cellpadding=1\" width=\"400\"\u003e \u003ctr align=\"center\"\u003e\n\n\u003ctd\u003e1st Test\u003c\/td\u003e\n\n\u003ctd\u003e2nd Test\u003c\/td\u003e\n\n\u003ctd\u003eInterpretation\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003ePositive\u003c\/td\u003e\n\n\u003ctd\u003ePositive\u003c\/td\u003e\n\n\u003ctd\u003eProbable perimenopause. Discuss methods and therapies to promote health after menopause with your doctor.\u003cbr\u003e DO NOT stop contraception immediately.\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003ePositive\u003cbr\u003eor\u003cbr\u003eNegative\u003c\/td\u003e\n\n\u003ctd\u003eNegative\u003cbr\u003eor\u003cbr\u003ePositive\u003c\/td\u003e\n\n\u003ctd\u003eProbable early stage of perimenopause.\u003cbr\u003e DO NOT stop contraception immediately.\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eNegative\u003c\/td\u003e\n\n\u003ctd\u003eNegative\u003c\/td\u003e\n\n\u003ctd\u003eProbably not yet in perimenopause. If symptoms persist, repeat the test next month or investigate other possible causes for the symptoms.\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003c\/table\u003e \u003cbr\u003e For women experiencing pre-menopause symptoms WITHOUT a menstrual cycle in the previous 12 months:\u003cbr\u003e \u003ctable border=\"1cellspacing=0cellpadding=1\" width=\"400\"\u003e \u003ctr align=\"center\"\u003e\n\n\u003ctd\u003e1st Test\u003c\/td\u003e\n\n\u003ctd\u003eInterpretation\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003ePositive\u003c\/td\u003e\n\n\u003ctd\u003eMenopause almost certainly in progress. The test can be repeated. Discuss methods and therapies to promote health after menopause with your doctor.\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003c\/table\u003e \u003cbr\u003e \u003cb\u003eLimitations\u003c\/b\u003e\u003cbr\u003e There is a possibility that this test may produce false positive or false negative results. Consult your doctor before making any medical decisions. Invalid results may be caused by not following the instructions carefully. Review the instructions and\/or repeat the test with a new device. If the problem persists, stop using the kit immediately and contact your local distributor.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Box containing 2 pieces.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eBIBLIOGRAPHY:\u003c\/u\u003e\u003cbr\u003e 1. Turkington CA. The Perimenopause Sourcebook. Contemporary Books, New York, NY. 1998.\u003cbr\u003e 2. Perry S, O’Hanlan K. Natural Menopause: The Complete Guide. Reading, MA, Addison-Wesley, 1997.\u003cbr\u003e 3. Stanford, JL, Weiss NS, et al. Combined Estrogen and Progestin Hormone Replacement Therapy in Relation to Risk of Breast Cancer, J. Am. Med. Assoc. 1995; 274(2): 137-142.\u003cbr\u003e 4. Speroff L, Glass RH, Kase NG, Clinical Gynecologic Endocrinology and Infertility 5th Ed, Williams and Wilkins, Baltimore, MD. 1994; 588.\u003cbr\u003e 5. Jacobs DS, Demott DR, Grady HJ, Horvat RT, Huestis DW, Kasten BL, Laboratory Test Handbook 4th Ed, Lippincott Williams and Wilkins, Baltimore, MD. 1996\u003c\/div\u003e","brand":"SCREEN ITALIA Srl","offers":[{"title":"Default Title","offer_id":45943379427595,"sku":"912359256","price":12.6,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_74b41bbf-f494-40e4-b16f-71efa0498693.jpg?v=1727809563"},{"product_id":"screen-droga-test-saliva-6-droghe","title":"SALIVA DRUG TEST SCREEN 6 DRUGS","description":"\u003ch2\u003e\n\n\u003ci\u003eSCREEN\u003c\/i\u003e\u003cbr\u003e DRUG TEST\u003cbr\u003e \u003cbr\u003e SALIVA 6\u003c\/h2\u003e \u003cdiv align=\"Justify\"\u003eRapid screening test for the simultaneous, qualitative detection of amphetamine, methamphetamine, cocaine, opiates, marijuana, ecstasy and their metabolites in human saliva.\u003cbr\u003e \u003cbr\u003e \u003cb\u003ePrecautions\u003c\/b\u003e\u003cbr\u003e • Product not for medical or diagnostic use.\u003cbr\u003e • Do not use beyond the expiration date.\u003cbr\u003e • Keep the reactive strip panel in the sealed pouch until use.\u003cbr\u003e • Store in the sealed pouch until use.\u003cbr\u003e • Saliva is not classified as a biohazard unless it comes from a dental procedure.\u003cbr\u003e • Used collector and Card must be disposed of in accordance with current regulations.\u003cbr\u003e \u003cbr\u003e \u003cbr\u003e \u003cb\u003eIntended Use and Summary\u003c\/b\u003e\u003cbr\u003e Chromatographic immunoassay for the qualitative detection of multiple drugs and metabolites in saliva at the following cut-off concentrations:\u003cbr\u003e \u003ctable border=\"1cellspacing=0cellpadding=1\" width=\"400\"\u003e \u003ctr\u003e\n\n\u003ctd\u003e\u003cb\u003eTest\u003c\/b\u003e\u003c\/td\u003e\n\n\u003ctd\u003e\u003cb\u003eCalibrator\u003c\/b\u003e\u003c\/td\u003e\n\n\u003ctd\u003e\u003cb\u003eCut-off (ng\/ml)\u003c\/b\u003e\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eAmphetamine (AMP)\u003c\/td\u003e\n\n\u003ctd\u003eD-Amphetamine \u003c\/td\u003e\n\n\u003ctd\u003e40\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eMethamphetamine (MET)\u003c\/td\u003e\n\n\u003ctd\u003e D-Methamphetamine\u003c\/td\u003e\n\n\u003ctd\u003e 40\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eMarijuana (THC)\u003c\/td\u003e\n\n\u003ctd\u003e 11-nor-Δ9-THC-9 COOH \u003c\/td\u003e\n\n\u003ctd\u003e10\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eCocaine (COC)\u003c\/td\u003e\n\n\u003ctd\u003e Benzoylecgonine\u003c\/td\u003e\n\n\u003ctd\u003e 30\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eOpiates (OPI\/MOP)\u003c\/td\u003e\n\n\u003ctd\u003e Morphine \u003c\/td\u003e\n\n\u003ctd\u003e40\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eEcstasy (MDMA)\u003c\/td\u003e\n\n\u003ctd\u003e D,L-methylenedioxymethamphetamine \u003c\/td\u003e\n\n\u003ctd\u003e50\u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\n\u003c\/table\u003e\n\n\u003cbr\u003e This test only provides preliminary analytical data.\u003cbr\u003e More specific chemical methods must be used to confirm the analytical result.\u003cbr\u003e Gas chromatography and mass spectrometry (GC\/MS) are considered preferred confirmatory methods.\u003cbr\u003e Any result for the determination of the presence of drugs of abuse must be correlated with clinical considerations and professional judgment, particularly when the preliminary result is positive.\u003cbr\u003e \u003cbr\u003e Rapid urine screening test that does not require the use of special instruments.\u003cbr\u003e The test uses antibodies to selectively detect high levels of specific substances in human saliva.\u003cbr\u003e The detection windows are approximate for each substance as they vary based on frequency of use, body mass, age, health status, and tolerance to narcotic substances.\u003cbr\u003e The product detects the presence of narcotic substances in saliva only after their metabolization.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCOCAINE (COC)\u003c\/b\u003e\u003cbr\u003e Cocaine is a powerful central nervous system stimulant as well as a local anesthetic derived from the coca plant.\u003cbr\u003e The substance is often self-administered by inhalation or intravenous injection or by smoking the base substance.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eAMPHETAMINE (AMP)\u003c\/b\u003e\u003cbr\u003e Amphetamine is a substance also used for therapeutic purposes.\u003cbr\u003e The substance is often self-administered by inhalation or ingestion.\u003cbr\u003e High doses produce enhanced central nervous system stimulation and induce euphoria, alertness, decreased appetite, and a sense of increased energy and strength.\u003cbr\u003e More acute reactions produce anxiety, paranoia, hallucinations, and psychotic behavior.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eMETHAMPHETAMINE (MET\/MDMA)\u003c\/b\u003e\u003cbr\u003e Methamphetamine is a potent stimulant chemically related to amphetamine, but with a greater capacity for central nervous system stimulation.\u003cbr\u003e The substance is often self-administered by inhalation, smoking, or ingestion.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eMARIJUANA (THC)\u003c\/b\u003e\u003cbr\u003e Tetrahydrocannabinol is the active ingredient in cannabis.\u003cbr\u003e When smoked or taken orally, THC produces euphoria.\u003cbr\u003e Regular users experience short-term memory impairment and learning difficulties, and may also have transient episodes of confusion and anxiety.\u003cbr\u003e Long-term relatively heavy use may be associated with behavioral disorders.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eOPIATES (OPI)\u003c\/b\u003e\u003cbr\u003e The opiate class refers to any substance derived from the opium poppy, including natural compounds such as morphine, codeine, and semi-synthetic substances such as heroin.\u003cbr\u003e Opiates act on pain control by depressing the central nervous system.\u003cbr\u003e Withdrawal symptoms may include sweating, tremors, nausea, and irritability.\u003cbr\u003e Opiates can be taken orally or by intravenous, intramuscular, and subcutaneous injection.\u003cbr\u003e Users may also take the substance intravenously or by inhalation.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eECSTASY (MDMA)\u003c\/b\u003e\u003cbr\u003e Synthetic drug, first synthesized in 1914 by a German pharmaceutical company for the treatment of obesity.\u003cbr\u003e Frequent users report side effects such as increased muscle tension and sweating.\u003cbr\u003e MDMA is not a true stimulant, although it shares with amphetamines the ability to increase blood pressure and heart rate.\u003cbr\u003e MDMA produces some perceptual changes such as increased light sensitivity, difficulty concentrating, and blurred vision in some users.\u003cbr\u003e Its mechanism of action is thought to involve the release of the neurotransmitter serotonin.\u003cbr\u003e MDMA can also release dopamine, although it is commonly believed that this is a secondary effect of the substance (Nichols and Oberlender, 1990).\u003cbr\u003e The most obvious effect of MDMA, which potentially occurs in all who have taken a reasonable dose of the substance, is jaw clenching.\u003cbr\u003e The test for MDMA contained in the product provides a positive result when the concentration of MDMA in saliva exceeds 50 ng\/ml.\u003cbr\u003e \u003cbr\u003e \u003cb\u003ePRINCIPLE\u003c\/b\u003e\u003cbr\u003e It is an immunoassay based on the principle of competitive binding.\u003cbr\u003e Drugs that may be present in the oral fluid sample compete against their respective conjugates for binding sites on the specific antibody.\u003cbr\u003e During the test, a portion of the saliva sample migrates upwards by capillary action.\u003cbr\u003e A drug, if present in the oral fluid sample below the cut-off concentration, will not saturate the binding sites of this specific antibody.\u003cbr\u003e The antibody will therefore react with the drug-protein conjugate and a colored line will appear in the test region for the specific drug being tested. The presence of the drug above the cut-off concentration will saturate all antibody binding sites.\u003cbr\u003e Thus, the colored line will not form in the test region.\u003cbr\u003e A positive oral fluid sample will not generate a colored line in the specific test region of the strip due to drug competition, while a negative oral fluid sample for the drug will generate a line in the test region due to the absence of competition.\u003cbr\u003e For procedural control, a colored line will always appear in the control region, indicating that a correct sample volume has been dispensed and that the membrane has been wet.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eREAGENTS\u003c\/b\u003e\u003cbr\u003e The test contains membrane strips coated with drug-protein conjugates (purified bovine albumin) on the test line, a goat polyclonal antibody against gold-protein conjugate on the control line, and an impregnated pad containing colloidal gold particles coated with a mouse monoclonal antibody specific for Amphetamine, Methamphetamine, Cocaine, Opiates, Δ9-thc-cooh, Methadone, Ecstasy and Synthetic Marijuana.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eSTORAGE AND STABILITY\u003c\/b\u003e\u003cbr\u003e Store in the original sealed package at 2-30°C.\u003cbr\u003e The test is stable until the expiration date printed on the package.\u003cbr\u003e The test must remain in the sealed package until use.\u003cbr\u003e Do not freeze.\u003cbr\u003e Do not use beyond the expiration date.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eSAMPLE COLLECTION AND PREPARATION\u003c\/b\u003e\u003cbr\u003e The oral fluid sample should be collected using the collector provided with the kit.\u003cbr\u003e Follow the detailed instructions below.\u003cbr\u003e Do not use other collection devices for analysis.\u003cbr\u003e Oral fluid can be collected at any time of day.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eINSTRUCTIONS FOR USE\u003c\/b\u003e\u003cbr\u003e Bring the test, sample and\/or controls to room temperature (15-30°C) before testing.\u003cbr\u003e Instruct the donor not to put anything in their mouth, including food, drink, gum, or tobacco, for at least 10 minutes before collection.\u003cbr\u003e 1. Bring the package to room temperature before opening. Remove the test from the sealed package and use within one hour.\u003cbr\u003e 2. Remove the test cap and insert the absorbent pad into the mouth, under the tongue, to collect saliva until the control line appears. Remove the test.\u003cbr\u003e 3. Place the test on a clean, flat surface. See illustration below. 4. Read the results after 10 minutes. Do not read the results after 1 hour.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eINTERPRETATION OF RESULTS\u003c\/b\u003e\u003cbr\u003e Negative*: all test bands appear. One colored line must be in the control region (C), while the other must be adjacent to the test region (Substance\/T). A negative result indicates that the substance concentration is below the detectable level or absent.\u003cbr\u003e \u003cfont size=\"2\"\u003e*the shade in the test region (Substance\/T) varies, but even a weakly colored line should be considered negative\u003c\/font\u003e\u003cbr\u003e Positive: only one colored line appears in the control region (C). No test band appears in the test region (Substance\/T). A positive result indicates that the substance concentration is above the detectable level.\u003cbr\u003e Invalid: no control line appears. The most probable reasons for the control line not appearing are insufficient sample volume or incorrect procedural techniques. Check the procedure and repeat the test using a new card.\u003cbr\u003e If the test result is positive, avoid aggressive behavior and calmly seek dialogue with the person concerned. Seek advice from your doctor, a psychologist, or contact the relevant service in your area.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eQUALITY CONTROL\u003c\/b\u003e\u003cbr\u003e A procedural control is included in the test.\u003cbr\u003e The line that appears in the control region (C) is considered an internal procedural control.\u003cbr\u003e It confirms that a sufficient sample volume has been used, adequate membrane wetting, and correct procedural technique.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eLIMITATIONS\u003c\/b\u003e\u003cbr\u003e 1. The test only provides a preliminary qualitative analytical result. A secondary analytical method is required to confirm the result. The recommended confirmatory method is gas chromatography\/mass spectrometry (GC\/MS).\u003cbr\u003e 2. A positive test result does not indicate the concentration of the substance in the sample or the route of administration.\u003cbr\u003e 3. A negative result may not necessarily indicate a drug-free sample. Negative results can be obtained when the drug is present below the test's cut-off level.\u003cbr\u003e 4. Technical or procedural errors, as well as interfering substances present in the saliva sample, may cause erroneous results.\u003cbr\u003e 5. This test does not distinguish between drugs of abuse and certain medications.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFORMAT\u003c\/b\u003e\u003cbr\u003e • 1 swab.\u003cbr\u003e • 1 Saliva Drug Test 6.\u003cbr\u003e • package insert.\u003c\/div\u003e","brand":"SCREEN ITALIA Srl","offers":[{"title":"Default Title","offer_id":45943652614411,"sku":"911151645","price":16.58,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_219b46ba-410c-40a3-8e89-3b83188b8752.jpg?v=1727810649"},{"product_id":"etiltest-alcol-test-saliva-1-pezzo","title":"ALCOHOL TEST SALIVA ALCOHOL TEST 1 PIECE","description":"\u003ch1\u003eALCOHOL TEST\u003cbr\u003e \u003cfont size=\"4\"\u003eSALIVA ALCOHOL TEST\u003c\/font\u003e\n\n\u003c\/h1\u003e Rapid Etil Test is an enzymatic test for the rapid and safe detection of the presence of alcohol (alc) (ethyl alcohol\/ethanol) in saliva and other liquid samples. By analyzing the saliva sample, the concentration of alcohol in the blood can be determined.\u003cbr\u003e This enzymatic analysis provides a qualitative result, meaning the test shows whether or not alcohol is present in the samples.\u003cbr\u003e The analysis detects an ethanol concentration of 0.1% or 10 mg\/dL, which is indicated by a light green-grey color of the reactive pad or test pad. The green color becomes more intense as the alcohol concentration in the sample increases. Therefore, in the presence of alcohol in the sample, Etil Test determines a color change ranging from light green-grey for an alcohol concentration of 0.1%, to a slightly more intense green for a medium concentration, up to a dark green-grey color if the alcohol concentration approaches 1.50%.\u003cbr\u003e We recommend using this visual test only as a qualitative test, as the human eye's discrimination ability can lead to errors in quantitative results.\u003cbr\u003e Measures 5 levels of alcohol in the body: 0.00 g\/l - 0.20 g\/l - 0.50 g\/l - 0.80 g\/l - 1.50 g\/l.\u003cbr\u003e The Etil Test consists of a plastic stick whose end is covered with a reactive pad. The pad, upon contact with alcohol solutions, rapidly changes color with shades from green to blue, depending on the amount of alcohol contained in the liquid. The reactive pad reacts based on a solid-phase chemical synthesis.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eHow to use\u003c\/b\u003e\u003cbr\u003e 1. Do not put anything in your mouth for fifteen (15) minutes before starting the test. This warning includes non-alcoholic beverages, tobacco products, coffee, breath mints, food, etc.\u003cbr\u003e 2. Bring the sealed pouch to room temperature (15-30°C) to avoid moisture condensation on the reactive pad.\u003cbr\u003e 3. If analyzing liquid samples other than saliva, ensure that these liquids are at room temperature before proceeding with the test.\u003cbr\u003e 4. Open the package and remove the stick. Observe the reactive pad located at the end of the stick. The pad should be light cream in color. A stick with a dark brown or stained reactive pad should be discarded.\u003cbr\u003e 5. Saturate the reactive pad with the liquid or with saliva collected from the mouth or a spittoon. Start the timer immediately.\u003cbr\u003e 6. After two (2) minutes, observe the color change (if any) on the reactive pad. If the pad turns green or dark green-grey, it means that the test has detected the presence of alcohol and the result is positive. Results obtained after more than 3 minutes may be incorrect.\u003cbr\u003e 7. Estimate the approximate blood alcohol concentration by comparing the color of the reactive pad with the color scale on the test package. We recommend using the visual test only as a qualitative test.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eInterpretation of results\u003c\/b\u003e\u003cbr\u003e After 2 minutes, read the color of the reactive pad. Do not compare the result of the stick with other color scales. Use only the color scale provided on the package. The reaction occurs more slowly in saliva than in other aqueous solutions.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eLimitations\u003c\/b\u003e\u003cbr\u003e If, after ingesting food, beverages or anything else, you do not wait at least 15 minutes before performing the test, the results could be incorrect due to the possible contamination of saliva with interfering substances.\u003cbr\u003e Etil Test has been designed and calibrated to be interpreted 2 minutes after wetting the reactive pad. If you wait more than 2 minutes, the results shown may be incorrect or false positive results may occur.\u003cbr\u003e Etil Test can be used to detect the presence of alcohol in fluids other than saliva. However, if used in this way, the color scale on the package cannot be used as a reference.\u003cbr\u003e If alcohol is present in the fluid, the pad will take on a color ranging from light green-grey to black or cocoa, as the alcohol concentration increases. If the pad is immersed in pure alcohol, the pad will color slightly or not at all, due to the absence of water which is necessary for the coloring reaction to occur.\u003cbr\u003e When analyzing beverages, the result can only be considered positive if the pad turns very dark brown.\u003cbr\u003e Etil Test is very sensitive to alcohol. Alcohol vapors often present in the air are sometimes detected by Etil Test.\u003cbr\u003e Alcohol vapors are often present in many public places and inside homes. Alcohol is found in many household cleaning products such as disinfectants, deodorants, and glass cleaners. If the presence of alcohol vapors is suspected, the test should be performed in an area where these vapors are not present (outdoors, for example).\u003cbr\u003e Note: the person reading the test results cannot be colorblind.\u003cbr\u003e \u003cbr\u003e\u003cb\u003eControls\u003c\/b\u003e\u003cbr\u003e The integrity of the Etil Test can be qualitatively verified by using a solution prepared by adding 4 drops of 40% vol distilled liquor to a glass of water.\u003cbr\u003e With this solution, the coloring should correspond to the window equal to or greater than 0.04% (darker).\u003cbr\u003e The color reaction with alcohol in saliva occurs more slowly and with less intense coloring than with alcohol in aqueous solutions.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFeatures\u003c\/b\u003e\u003cbr\u003e Specificity: ethyl test will react in the presence of methyl, ethyl, and allyl alcohol. Etil Test will not produce any reaction with alcohols containing 5 or more carbon atoms, nor with glycine, glycerol, or serine.\u003cbr\u003e This property derives from the specificity of the alcohol oxidase enzyme extracted from yeast.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eInteractions\u003c\/b\u003e\u003cbr\u003e The following substances may interfere with the Etil Test stick if liquid samples other than saliva are used:\u003cbr\u003e \u003cu\u003eColor-intensifying agents:\u003c\/u\u003e\u003cbr\u003e - Peroxide.\u003cbr\u003e - Strong oxidizing agents.\u003cbr\u003e - (common in detergents, stripping agents, and bleaches).\u003cbr\u003e \u003cu\u003eColor-inhibiting agents:\u003c\/u\u003e\u003cbr\u003e Reducing agents:\u003cbr\u003e - Ascorbic acid.\u003cbr\u003e - Tannic acid.\u003cbr\u003e - Pyrogallol.\u003cbr\u003e - Mercaptans and tosylates.\u003cbr\u003e - Oxalic acid.\u003cbr\u003e - Uric acid.\u003cbr\u003e - Bilirubin.\u003cbr\u003e - L-dopamine.\u003cbr\u003e - L-methyldopamine.\u003cbr\u003e - Metampyrone.\u003cbr\u003e The aforementioned substances are usually not present in saliva in quantities sufficient to interfere with the test. However, it is necessary that they are not introduced into the mouth within 15 minutes prior to the test.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e - Single use.\u003cbr\u003e - Product not intended for medical or diagnostic purposes.\u003cbr\u003e - Do not use after the expiration date.\u003cbr\u003e - Allow the reactive pad to absorb enough liquid to completely saturate it.\u003cbr\u003e - Do not eat, drink, or smoke while samples or the kit are being handled.\u003cbr\u003e - Do not use the test if the pouch is damaged.\u003cbr\u003e - Bring reagents to room temperature (15-30°C) before use.\u003cbr\u003e - Do not touch the reactive pad on the stick to avoid contamination.\u003cbr\u003e - Avoid cross-contamination between samples by using a new collection container for each sample.\u003cbr\u003e - Not for medical or diagnostic use.\u003cbr\u003e - Handle all samples as if they contain infectious agents. During the test, observe precautions against microbiological risks and follow standard procedures for proper sample disposal.\u003cbr\u003e - Leave the stick in the sealed pouch until it is used.\u003cbr\u003e - Observe the test result after 2-3 minutes.\u003cbr\u003e - Humidity and high temperatures can affect test results.\u003cbr\u003e - Do not perform the test in an atmosphere containing alcohol.\u003cbr\u003e - Pure alcohol can give false results.\u003cbr\u003e - Pay attention to possible cross-reactivities.\u003cbr\u003e - We recommend using the visual test only as a qualitative test.\u003cbr\u003e - The person reading the results cannot be colorblind.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eStorage\u003c\/b\u003e\u003cbr\u003e The test kit should be stored in the refrigerator or at room temperature (2-30°C) in the sealed pouch, according to the product's shelf life.\u003cbr\u003e Bring the stick to room temperature to prevent moisture condensation on the reactive pad.\u003cbr\u003e \u003cbr\u003e \u003cb\u003e Composition\/Ingredient information\u003c\/b\u003e\u003cbr\u003e Complete kit composition:\u003cbr\u003e - Test strip: contains a filter paper pad with alcohol oxidase, peroxidase, 3,3,5,5-tetramethylbenzidine (TMB), and TRIS-HCl buffer in a dry state.\u003cbr\u003e - The test strip consists of: PE catalyst, filter paper reagent pad.\u003cbr\u003e - Other components: aluminum pouch, hygroscopic silica gel.\u003cbr\u003e Harmful components:\u003cbr\u003e none.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Pack of 1 piece.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCode.\u003c\/b\u003e CALC1S","brand":"NOI TEST Srl","offers":[{"title":"Default Title","offer_id":45943681974539,"sku":"930864792","price":1.78,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_11e73a70-8258-4f1b-93ba-addeeabd927b.jpg?v=1727810743"},{"product_id":"screen-droga-test-5-droghe-test-antidroga-con-contenitore-urina","title":"SCREEN DRUG TEST 5 DRUGS DRUG TEST WITH URINE CONTAINER","description":"\u003ch2\u003e\n\n\u003ci\u003eSCREEN\u003c\/i\u003e\u003cbr\u003e DRUG TEST\u003cbr\u003e \u003cbr\u003e URINE 5\u003c\/h2\u003e \u003cdiv align=\"justify\"\u003eInstructions for use for each test combination of the following drugs: amphetamine, methamphetamine, cocaine, marijuana, and opiates.\u003cbr\u003e One-step test for the simultaneous qualitative determination of drugs and their metabolites in human urine.\u003cbr\u003e \u003cbr\u003e \u003cb\u003ePRECAUTIONS\u003c\/b\u003e\u003cbr\u003e Product not intended for medical or diagnostic use.\u003cbr\u003e • Do not use beyond the expiration date.\u003cbr\u003e • Store the test strip panel in the sealed pouch until use.\u003cbr\u003e • All samples must be considered potentially hazardous and, therefore, must be handled with the precautions related to potentially infectious products.\u003cbr\u003e • After use, the panel must be disposed of according to current local regulations.\u003cbr\u003e Store in the sealed pouch at a temperature between 2° and 30°C.\u003cbr\u003e The test strip panel is stable until the expiration date indicated on the pouch label.\u003cbr\u003e The test strip panel must be stored in the sealed pouch until use.\u003cbr\u003e Do not freeze.\u003cbr\u003e Do not use beyond the expiration date.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eINTENDED USE AND SUMMARY\u003c\/b\u003e\u003cbr\u003e Screening test for the simultaneous determination of various drugs.\u003cbr\u003e The speed and sensitivity of immunological tests have led them to be considered the most accepted as screening tests in urine for the simultaneous detection of drugs of abuse.\u003cbr\u003e The one-step test strip panel (Urine) is a rapid lateral flow immunochromatographic test for the qualitative determination of the following drugs without the aid of instruments.\u003cbr\u003e \u003cbr\u003e \u003ctable border=\"1cellspacing=0cellpadding=1\" width=\"400\"\u003e \u003ctr\u003e\n\n\u003ctd\u003e\u003cb\u003eTest\u003c\/b\u003e\u003c\/td\u003e\n\n\u003ctd\u003e\u003cb\u003e Calibrator\u003c\/b\u003e\u003c\/td\u003e\n\n\u003ctd\u003e\u003cb\u003e Cut-off (ng\/ml)\u003c\/b\u003e\u003c\/td\u003e \u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eCocaine (COC)\u003c\/td\u003e\n\n\u003ctd\u003e benzoylecgonine\u003c\/td\u003e\n\n\u003ctd\u003e 300\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eAmphetamine (AMP)\u003c\/td\u003e\n\n\u003ctd\u003e D-amphetamine \u003c\/td\u003e\n\n\u003ctd\u003e1,000\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003e Methamphetamine (mAMP) \u003c\/td\u003e\n\n\u003ctd\u003eD-methamphetamine\u003c\/td\u003e\n\n\u003ctd\u003e 1,000\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eMarijuana (THC) \u003c\/td\u003e\n\n\u003ctd\u003e11-nor-Δ9-THC-9 COOH\u003c\/td\u003e\n\n\u003ctd\u003e50\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eOpiates (OPI) \u003c\/td\u003e\n\n\u003ctd\u003emorphine\u003c\/td\u003e\n\n\u003ctd\u003e 2,000\u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\n\u003c\/table\u003e\n\n\u003cbr\u003e This test only provides preliminary analytical data. More specific chemical methods must be used to confirm the analytical result.\u003cbr\u003e Gas chromatography and mass spectrometry (GC\/MS) are considered preferred confirmatory methods.\u003cbr\u003e Any result for the determination of the presence of drugs of abuse must be correlated with clinical considerations and professional judgment, particularly when the preliminary result is positive.\u003cbr\u003e Rapid urine screening test that does not require the use of special instruments.\u003cbr\u003e The test uses antibodies to selectively detect high levels of specific substances in human urine.\u003cbr\u003e Retention times are approximate for each substance as they vary depending on frequency of use, body mass, age, health status, tolerance to narcotic substances, and urine pH.\u003cbr\u003e It detects the presence of narcotic substances in urine only after their metabolism.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eCOCAINE (COC)\u003c\/u\u003e\u003cbr\u003e Cocaine is a potent central nervous system stimulant as well as a local anesthetic derived from the coca plant.\u003cbr\u003e The substance is often self-administered by inhalation or intravenous injection or by smoking the base substance.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eAMPHETAMINE (AMP)\u003c\/u\u003e\u003cbr\u003e Amphetamine is a substance also used for therapeutic purposes.\u003cbr\u003e The substance is often self-administered by inhalation or ingestion.\u003cbr\u003e High doses produce enhanced central nervous system stimulation and induce euphoria, alertness, reduced appetite, and a feeling of increased energy and strength.\u003cbr\u003e More acute reactions produce anxiety, paranoia, hallucinations, and psychotic behavior.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eMETHAMPHETAMINE (mAMP)\u003c\/u\u003e\u003cbr\u003e Methamphetamine is a powerful stimulant chemically related to amphetamine, but with a greater capacity for central nervous system stimulation.\u003cbr\u003e The substance is often self-administered by inhalation, smoking, or ingestion.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eMARIJUANA (THC)\u003c\/u\u003e\u003cbr\u003e Tetrahydrocannabinol is the active ingredient in cannabis.\u003cbr\u003e When smoked or taken orally, THC produces euphoria.\u003cbr\u003e Habitual users experience short-term memory impairment and learning difficulties, and may also have transient episodes of confusion and anxiety.\u003cbr\u003e Long-term, relatively heavy consumption may be associated with behavioral disorders.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eOPIATES (OPI)\u003c\/u\u003e\u003cbr\u003e The opiate class refers to any substance derived from the opium poppy, including natural compounds such as morphine, codeine, and semi-synthetic substances like heroin.\u003cbr\u003e Opiates act on pain control by depressing the central nervous system.\u003cbr\u003e Withdrawal symptoms may include sweating, tremors, nausea, and irritability.\u003cbr\u003e Opiates can be taken orally or by intravenous, intramuscular, and subcutaneous injection.\u003cbr\u003e Users may also take the substance intravenously or by inhalation.\u003cbr\u003e \u003cbr\u003e \u003cb\u003ePRINCIPLE\u003c\/b\u003e\u003cbr\u003e The one-step test strip panel (Urine) is a rapid immunochromatographic test based on the principle of competitive binding.\u003cbr\u003e Drugs that may be present in the urine sample compete with the corresponding conjugate for the same antibody binding sites.\u003cbr\u003e During the test, a urine sample migrates by capillarity along the membrane.\u003cbr\u003e A drug, if present in the urine sample at a concentration below its cut-off, will not be able to saturate all binding sites of the antibody-bound particles present in the strip.\u003cbr\u003e The antibody-bound particles will be captured by the immobilized conjugate, and a visible colored band will appear in the test band region of the corresponding strip.\u003cbr\u003e The colored band will not form in the corresponding area if the drug level is above its cut-off, as all binding sites of the corresponding antibodies will be saturated.\u003cbr\u003e A urine sample positive for the drug being tested will not cause the formation of the colored band due to drug competition, while a urine sample negative for the drug being tested or a sample containing a drug concentration below the cut-off will cause the formation of the colored band in the specific test area.\u003cbr\u003e As a procedural control, a colored band will appear in the corresponding area, indicating that a correct amount of sample has been used and that migration on the membrane has occurred.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eREAGENTS\u003c\/b\u003e\u003cbr\u003e Each strip of the panel contains mouse monoclonal antibodies bound to particles and the corresponding.\u003cbr\u003e The one-step test strip panel (Urine) is a rapid lateral flow immunochromatographic test conjugated for each drug.\u003cbr\u003e Goat antibodies are used for the control band.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eSAMPLE COLLECTION AND PREPARATION\u003c\/b\u003e\u003cbr\u003e Collect the urine sample in a clean and dry container.\u003cbr\u003e Urine samples collected at any time of day can be used.\u003cbr\u003e Urine samples with obvious precipitate must be centrifuged, filtered, or allowed to settle to obtain a clear sample for testing.\u003cbr\u003e Urine samples can be stored at 2-8°C for a maximum of 48 hours.\u003cbr\u003e For prolonged storage, samples can be frozen and stored at temperatures below -20°C.\u003cbr\u003e Before using frozen samples, they must be thawed and thoroughly homogenized.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eOPERATING PROCEDURE\u003c\/b\u003e\u003cbr\u003e 1. Before opening the pouch, bring it to room temperature.\u003cbr\u003e Remove the product from the pouch and use it as soon as possible.\u003cbr\u003e 2. Remove the caps from the strips. Dip the product vertically, in the direction of the arrows, into the urine sample for at least 10\/15 seconds. Dip the product up to the level of the wavy lines on the strips but not above them.\u003cbr\u003e 3. Replace the cap on the device and place the product horizontally on a flat, non-absorbent surface. Read the result after 5 minutes. Do not interpret the result after 10 minutes.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eINTERPRETATION OF RESULTS\u003c\/b\u003e\u003cbr\u003e Negative*: A colored band appears in the control region (C) and a second in the test region (T) for each drug, indicating a negative result. A negative result indicates that the concentration of the drug in question in the urine is below the detectable cut-off level for that specific drug.\u003cbr\u003e \u003cfont size=\"2\"\u003e*the shade of color in the test region (T) may vary, but any faint colored band should be considered negative.\u003c\/font\u003e\u003cbr\u003e Positive: A colored band appears in the control region (C) but not in the test region (T) for each drug, indicating a positive result. A positive result indicates that the concentration of the drug in question in the urine is above the detectable cut-off level for that specific drug.\u003cbr\u003e Invalid: No control band (C) appears. The most plausible causes for the absence of the control band may be an insufficient sample volume or incorrect analytical procedure.\u003cbr\u003e Recheck the procedure and repeat the test using a new panel. If the problem persists, stop using the kit immediately and contact your local distributor.\u003cbr\u003e If the test result is positive, avoid aggressive behavior and calmly seek dialogue with the person concerned.\u003cbr\u003e Seek advice from your doctor, a psychologist, or contact the relevant service in your area.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eQUALITY CONTROL\u003c\/b\u003e\u003cbr\u003e The test includes an internal control system consisting of the red band that appears in the control region (C).\u003cbr\u003e The appearance of this band confirms that the test has been performed correctly with a sufficient sample volume, that membrane absorption was adequate, and the procedure was correct.\u003cbr\u003e Standard controls are not provided with the kit; however, it is recommended to test positive and negative controls, as good laboratory practice, to confirm the test procedure and verify its correct characteristics.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eLIMITATIONS\u003c\/b\u003e\u003cbr\u003e 1. The one-step test strip panel (Urine) only provides a preliminary qualitative analytical result. A second analytical method is required. Gas chromatography and mass spectrometry (GC\/MS) are considered preferred confirmatory methods if the test result is positive.\u003cbr\u003e 2. Technical or procedural errors, as well as interfering substances present in the urine sample, may cause incorrect results.\u003cbr\u003e 3. Adulterants, such as bleach and\/or alum present in the urine sample, may cause erroneous results regardless of the analytical method used. If the presence of such substances is suspected, the test should be repeated with another urine sample.\u003cbr\u003e 4. A positive result indicates the presence of the drug or its metabolites but not the level of intoxication, the route of administration, or the concentration in the urine.\u003cbr\u003e 5. A negative result does not necessarily mean that the urine sample is drug-free. A negative result can be obtained when the drug is present but at a concentration below the test's cut-off level.\u003cbr\u003e 6. The test cannot distinguish between the drug and a medication containing the same substance; false positives may be caused by certain medications.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFORMAT\u003c\/b\u003e\u003cbr\u003e • 1 urine container.\u003cbr\u003e • 1 Drug Test Urine 5.\u003cbr\u003e • 1 instruction leaflet.\u003c\/div\u003e","brand":"SCREEN ITALIA Srl","offers":[{"title":"Default Title","offer_id":45943692263691,"sku":"911151633","price":15.42,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_4b23667a-e0bd-418c-b1da-7633cc5df813.jpg?v=1727810769"},{"product_id":"screen-droga-test-cocaina-test-antidroga-con-contenitore-urina","title":"SCREEN DRUG TEST COCAINE DRUG TEST WITH URINE CONTAINER","description":"\u003ch2\u003e\n\n\u003ci\u003eSCREEN\u003c\/i\u003e\u003cbr\u003e DRUG TEST\u003cbr\u003e \u003cbr\u003e Cocaine\u003c\/h2\u003e \u003cdiv align=\"justify\"\u003eInstructions for use for each test combination of the following drugs: amphetamine, benzodiazepine, cocaine, marijuana, methylenedioxymethamphetamine, ketamine, opiates, synthetic marijuana k2\/spice.\u003cbr\u003e One-step test for the simultaneous qualitative determination of drugs and their metabolites in human urine.\u003cbr\u003e \u003cbr\u003e \u003cb\u003ePrecautions\u003c\/b\u003e\u003cbr\u003e Product not intended for medical or diagnostic use.\u003cbr\u003e Do not use beyond the expiration date.\u003cbr\u003e Store the test strip panel in the sealed pouch until use.\u003cbr\u003e All samples must be considered potentially hazardous and therefore handled with the precautions related to potentially infectious products.\u003cbr\u003e After use, the panel must be disposed of according to local regulations in force.\u003cbr\u003e Store in the sealed pouch at a temperature between 2° and 30°C.\u003cbr\u003e The test strip panel is stable until the expiration date indicated on the pouch label.\u003cbr\u003e The test strip panel must be stored in the sealed pouch until use.\u003cbr\u003e Do not freeze.\u003cbr\u003e Do not use beyond the expiration date.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eIntended Use and Summary\u003c\/b\u003e\u003cbr\u003e Screening test for the simultaneous determination of several drugs.\u003cbr\u003e The speed and sensitivity of immunoassays have made them considered the most accepted as screening tests in urine for the simultaneous detection of drugs of abuse.\u003cbr\u003e The one-step test strip panel (Urine) is a rapid lateral flow immunochromatographic test for the qualitative determination of the following drugs without the aid of instruments:\u003cbr\u003e \u003ctable border=\"1cellspacing=0cellpadding=1\" width=\"600\"\u003e \u003ctr align=\"center\"\u003e\n\n\u003ctd\u003e\u003cb\u003eTest\u003c\/b\u003e\u003c\/td\u003e\n\n\u003ctd\u003e\u003cb\u003eCalibrator\u003c\/b\u003e\u003c\/td\u003e \u003ctd\u003e\u003cb\u003eCut-off (ng\/ml)\u003c\/b\u003e\u003c\/td\u003e\n\n\n\u003c\/tr\u003e \u003ctr\u003e\n\n\u003ctd\u003eCocaine (COC)\u003cbr\u003e Amphetamine (AMP)\u003cbr\u003e Methylenedioxymethamphetamine (MDMA)\u003cbr\u003e Marijuana (THC)\u003cbr\u003e Opiates (OPI)\u003cbr\u003e Benzodiazepine (BZO)\u003cbr\u003e Ketamine (KET)\u003cbr\u003e Synthetic Marijuana k2\/spice\u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003eBenzoylecgonine\u003cbr\u003e D-Amphetamine\u003cbr\u003e D,L-Methylenedioxymethamphetamine\u003cbr\u003e 11-nor-Δ\u003csup\u003e9\u003c\/sup\u003e-THC-9 COOH\u003cbr\u003e Morphine\u003cbr\u003e Oxazepam\u003cbr\u003e Ketamine\u003cbr\u003e JWH-018 and JWH-073\u003c\/td\u003e\n\n\u003ctd align=\"center\"\u003e300\u003cbr\u003e 1,000\u003cbr\u003e 500\u003cbr\u003e 50\u003cbr\u003e 2,000\u003cbr\u003e 300\u003cbr\u003e 1000\u003cbr\u003e 50\u003c\/td\u003e\n\n\n\u003c\/tr\u003e\n\n\n\u003c\/table\u003e \u003cbr\u003e This test provides only preliminary analytical data.\u003cbr\u003e More specific chemical methods must be used to confirm the analytical result.\u003cbr\u003e Gas chromatography and mass spectrometry (GC\/MS) are considered preferential confirmatory methods.\u003cbr\u003e Any result for the determination of the presence of drugs of abuse must be correlated with clinical considerations and professional judgment, particularly when the preliminary result is positive.\u003cbr\u003e It is a rapid urine screening test that does not require the use of special instruments.\u003cbr\u003e The test uses antibodies to selectively detect high levels of specific substances in human urine.\u003cbr\u003e \u003cbr\u003e Retention times are approximate for each substance as they vary depending on frequency of use, body mass, age, health status, tolerance to narcotic substances, and urine pH.\u003cbr\u003e The product detects the presence of narcotic substances in urine only after their metabolization.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eCOCAINE (COC)\u003c\/u\u003e\u003cbr\u003e Cocaine is a potent central nervous system stimulant and local anesthetic derived from the coca plant.\u003cbr\u003e The substance is often self-administered by inhalation or intravenous injection, or by smoking the base substance.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eAMPHETAMINE (AMP)\u003c\/u\u003e\u003cbr\u003e Amphetamine is a substance also used for therapeutic purposes.\u003cbr\u003e The substance is often self-administered by inhalation or ingestion.\u003cbr\u003e High doses produce enhanced central nervous system stimulation and induce euphoria, alertness, appetite reduction, a sense of increased energy and strength.\u003cbr\u003e More acute reactions produce anxiety, paranoia, hallucinations, and psychotic behavior.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eMETHYLENEDIOXYMETHAMPHETAMINE (MDMA)\u003c\/u\u003e\u003cbr\u003e Ecstasy is not a stimulant, although it shares with amphetamines the ability to increase blood pressure and heart rate.\u003cbr\u003e It produces some changes in perception such as increased light sensitivity, difficulty focusing, blurred vision.\u003cbr\u003e The effect that occurs in almost everyone who takes this substance is jaw clenching.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eMARIJUANA (THC)\u003c\/u\u003e\u003cbr\u003e Tetrahydrocannabinol is the active ingredient in cannabis.\u003cbr\u003e When smoked or taken orally, THC produces euphoria.\u003cbr\u003e Regular users experience short-term memory impairment and learning difficulties, and may also have transient episodes of confusion and anxiety.\u003cbr\u003e Long-term relatively heavy use may be associated with behavioral disorders.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eOPIATES (OPI)\u003c\/u\u003e\u003cbr\u003e The opiate class refers to any substance derived from the opium poppy, including natural compounds such as morphine, codeine, and semi-synthetic substances like heroin.\u003cbr\u003e Opiates act on pain control by depressing the central nervous system.\u003cbr\u003e Withdrawal symptoms may include sweating, tremors, nausea, and irritability.\u003cbr\u003e Opiates can be taken orally or by intravenous, intramuscular, and subcutaneous injection.\u003cbr\u003e Users may also take the substance intravenously or by inhalation.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eBENZODIAZEPINE (BZO)\u003c\/u\u003e\u003cbr\u003e These are frequently prescribed medications for the symptomatic treatment of anxiety, sleep disorders, epileptic seizures, and alcohol withdrawal syndrome.\u003cbr\u003e Abrupt discontinuation can induce symptoms such as sleep disturbances, gastrointestinal issues, loss of appetite, sweating, tremors, weakness, anxiety, and changes in perception.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eKETAMINE (KET)\u003c\/u\u003e\u003cbr\u003e Ketamine is a dissociative anesthetic for human and veterinary use.\u003cbr\u003e It is marketed in Italy under the names Ketalar, Ketanest, and Ketaset, and in human medicine it is classified as a Class H drug and should only be used in a hospital setting by an anesthesiologist-resuscitator.\u003cbr\u003e Like all neuro- and psycholeptic drugs, it can be abused and used for recreational purposes, which is prohibited and penalized by law, as a narcotic substance.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eSYNTHETIC MARIJUANA K2\/SPICE (K2\/SPICE)\u003c\/u\u003e\u003cbr\u003e Synthetic Marijuana or K2 is a psychoactive herb and a chemical product that, when consumed, mimics the effects of Marijuana.\u003cbr\u003e Most commonly known by the trade names K2 and Spice, both widely used to refer to any synthetic Marijuana product.\u003cbr\u003e \u003cbr\u003e \u003cb\u003ePrinciple\u003c\/b\u003e\u003cbr\u003e The one-step test strip panel (Urine) is a rapid immunochromatographic test based on the principle of competitive binding.\u003cbr\u003e Drugs that may be present in the urine sample compete with their respective conjugate for the same antibody binding sites.\u003cbr\u003e During the test, a urine sample migrates by capillarity along the membrane.\u003cbr\u003e A drug, if present in the urine sample at a concentration below its cut-off, will not be able to saturate all binding sites of the antibody-bound particles present on the strip.\u003cbr\u003e The antibody-bound particles will be captured by the immobilized conjugate and a colored band will appear in the test band area of the respective strip.\u003cbr\u003e The colored band will not form in the respective area if the drug level is above its cut-off, as all binding sites of the respective antibodies will be saturated.\u003cbr\u003e A urine sample positive for the tested drug will not cause the formation of the colored band due to drug competition, while a urine sample negative for the tested drug or a sample containing a drug concentration below the cut-off will cause the formation of the colored band in the specific test area.\u003cbr\u003e As a procedural control, a colored band will appear in the control area, indicating that a correct amount of sample was used and that membrane migration occurred.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eReagents\u003c\/b\u003e\u003cbr\u003e Each strip of the panel contains mouse monoclonal antibodies bound to particles and the corresponding.\u003cbr\u003e The one-step test strip panel (Urine) is a rapid lateral flow immunochromatographic test conjugated for each drug.\u003cbr\u003e Goat antibodies are used for the control band.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eSample Collection and Preparation\u003c\/b\u003e\u003cbr\u003e Collect the urine sample in a clean and dry container.\u003cbr\u003e Urine samples collected at any time of day can be used.\u003cbr\u003e Urine samples with obvious presence of precipitate must be centrifuged, filtered, or allowed to settle to obtain a clear sample for testing.\u003cbr\u003e Urine samples can be stored at a temperature of 2-8°C for a maximum of 48 hours.\u003cbr\u003e For prolonged storage, samples can be frozen and stored at a temperature below -20°C.\u003cbr\u003e Before using frozen samples, they must be thawed and thoroughly homogenized.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eProcedure for use\u003c\/b\u003e\u003cbr\u003e 1. Before opening the pouch, bring it to room temperature. Remove the product from the pouch and use it as soon as possible.\u003cbr\u003e 2. Remove the cap from the strips. Immerse the product vertically, in the direction of the arrows, into the urine sample for at least 10\/15 seconds. Immerse the product up to the wavy lines on the strips but not above them.\u003cbr\u003e 3. Replace the cap on the device and place the product horizontally on a flat, non-absorbent surface. Read the result after 5 minutes. Do not interpret the result after 10 minutes.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eInterpretation of Results\u003c\/b\u003e\u003cbr\u003e \u003cu\u003eNegative*:\u003c\/u\u003e A colored band appears in the control region (C) and a second one in the test region (T) for each drug, indicating a negative result.\u003cbr\u003e A negative result indicates that the concentration of the drug in question in the urine is below the detectable cut-off level for that specific drug.\u003cbr\u003e \u003cfont size=\"2\"\u003e*the color intensity in the test region (T) may vary, but any faint colored band should be considered negative.\u003c\/font\u003e\u003cbr\u003e \u003cu\u003ePositive:\u003c\/u\u003e A colored band appears in the control region (C) but not in the test region (T) for each drug, indicating a positive result.\u003cbr\u003e A positive result indicates that the concentration of the drug in question in the urine is above the detectable cut-off level for that specific drug.\u003cbr\u003e \u003cu\u003eInvalid:\u003c\/u\u003e No control band (C) appears.\u003cbr\u003e The most plausible causes for the absence of the control band may be insufficient sample volume or incorrect analytical procedure.\u003cbr\u003e Recheck the procedure and repeat the test using a new panel.\u003cbr\u003e If the problem persists, immediately discontinue use of the kit and contact your local distributor.\u003cbr\u003e If the test result is positive, avoid aggressive behavior and calmly seek dialogue with the person concerned.\u003cbr\u003e Consult your doctor, a psychologist, or contact the relevant service in your area.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eQuality Control\u003c\/b\u003e\u003cbr\u003e The test includes an internal control system consisting of the red band that appears in the control region (C).\u003cbr\u003e The appearance of this band confirms that the test was performed correctly with a sufficient sample volume, that membrane absorption was adequate, and the procedure was correct.\u003cbr\u003e Standard controls are not provided with the kit; however, it is recommended to test positive and negative controls, as good laboratory practice, to confirm the test procedure and verify its correct characteristics.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eLimitations\u003c\/b\u003e\u003cbr\u003e 1. The one-step test strip panel (Urine) provides only a preliminary qualitative analytical result. A second analytical method is required. Gas chromatography and mass spectrometry (GC\/MS) are considered preferential confirmatory methods and are the recommended confirmatory methods if the test is positive.\u003cbr\u003e 2. It is possible that technical or procedural errors, as well as interfering substances present in the urine sample, may cause erroneous results.\u003cbr\u003e 3. It is possible that adulterants, such as bleach and\/or alum present in the urine sample, may cause erroneous results regardless of the analytical method used. If the presence of such substances is suspected, the test should be repeated with another urine sample.\u003cbr\u003e 4. A positive result indicates the presence of the drug or its metabolites but not the level of intoxication, the route of administration, or the concentration in the urine.\u003cbr\u003e 5. A negative result does not necessarily mean that the urine sample is drug-free. A negative result can be obtained when the drug is present but at a concentration below the test's cut-off level.\u003cbr\u003e 6. The test is unable to distinguish between the drug and a medication containing the same substance; false positives may be caused by some medications.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e • 1 urine container.\u003cbr\u003e • 1 Cocaine Drug Test.\u003cbr\u003e • insert.\u003c\/div\u003e","brand":"SCREEN ITALIA Srl","offers":[{"title":"Default Title","offer_id":45943819632907,"sku":"911151672","price":8.05,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_a81b5cbe-b103-47a3-b052-ff8eccdcab9c.jpg?v=1727811235"},{"product_id":"contenitore-urina-provetta-medipresteril","title":"URINE CONTAINER + MEDIPRESTERIL TUBE","description":"\u003ch1\u003eURINE CONTAINER + MEDIPRESTERIL TEST TUBE\u003cdiv align=\"justify\"\u003eSterile container for urine sampling and vacuum test tube.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e 120 ml container + 10 ml test tube.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCode.\u003c\/b\u003e P0405\u003c\/div\u003e\n\n\n\u003c\/h1\u003e","brand":"CORMAN SpA","offers":[{"title":"Default Title","offer_id":45944174838027,"sku":"926562810","price":1.19,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_d13cc269-7c87-46cc-aad0-44c497fb4be8.jpg?v=1727813151"},{"product_id":"test-autodiagnostico-one-step-strep-a-rilevazione-qualitativa-antigene-streptococco-a-in-tamponi-faringei","title":"ONE STEP STREP A SELF-TEST QUALITATIVE DETECTION OF STREPTOCOCCUS A ANTIGEN IN THROAT SWABS","description":"\u003ch2\u003eWondfo\u003c\/h2\u003e \u003ch1\u003eStreptococcus A\u003c\/h1\u003e \u003cdiv align=\"justify\"\u003e \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e Immunological lateral flow test for the qualitative detection of group A streptococcal antigen from pharyngeal swab samples to aid in the early diagnosis of group A Streptococcus infection.\u003cbr\u003e When the sample is added to the sample well, capillary action causes the sample to migrate across the membrane. When group A streptococcal antigen levels in the samples are equal to or greater than the cut-off, a visible colored line appears in the test zone, indicating a positive result. The absence of such a colored line in the Test (T) zone suggests a negative result. If the test has been performed correctly, a colored line will appear in the control (C) zone as a procedural control.\u003cbr\u003e For in vitro self-diagnostic use.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eInstructions for use\u003c\/b\u003e\u003cbr\u003e \u003cu\u003eSample collection and preparation\u003c\/u\u003e\u003cbr\u003e Collect the sample with the sterile pharyngeal swab provided in the kit. Hold the tongue down with a tongue depressor. Swab the back of the pharynx, tonsils, and other inflamed areas. Avoid touching the tongue, cheeks, and teeth with the swab.\u003cbr\u003e The test should ideally be performed immediately after sample collection.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eTest procedure\u003c\/u\u003e\u003cbr\u003e Bring the device and extraction reagents to room temperature (10 °C-30 °C) before performing the test.\u003cbr\u003e Add 4 drops of extraction reagent A and 4 drops of reagent B to the respective extraction tube and mix thoroughly.\u003cbr\u003e Place the sample extraction swab into the tube. Shake the swab ten times. Leave the swab in the tube for one minute. Then remove the swab while squeezing the head of the swab against the inside of the tube as you remove it to eliminate as much liquid as possible from the swab. Discard the swab.\u003cbr\u003e Cap the tube and mix the contents by gently shaking.\u003cbr\u003e The sample must be tested immediately.\u003cbr\u003e Remove the test from the sealed foil pouch by tearing at the notch and place the test on a clean, dry, flat surface. Add 3 drops of mixed liquid sample from the tube to the sample well (depicting an arrow) of the test cassette by inverting and squeezing the tube.\u003cbr\u003e Wait 10 minutes and read the results. Do not read the results after 15 minutes.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eReading the results\u003c\/u\u003e\u003cbr\u003e POSITIVE: If two colored lines are visible in both the test zone (T) and the control area (C), the result is positive. This indicates that a Group A Strep infection may be present and you should consult your doctor.\u003cbr\u003e \u003cbr\u003e NEGATIVE: If only one colored line appears in the control zone (C) and no colored line appears in the test zone (T), the result is negative. This indicates that the concentration of Group A Streptococcus antigen is at or below the test's detection limit.\u003cbr\u003e \u003cbr\u003e INVALID: No line visible or only one line visible in the test zone (T) but not in the control zone (C). This is an indication of a procedural error and\/or that the test reagent has deteriorated. Repeat the test with a new kit. If the test still proves invalid, please contact the distributor or the store where the product was purchased, providing the lot number.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e This kit is for in vitro self-diagnostic use only.\u003cbr\u003e Do not ingest.\u003cbr\u003e Do not interchange caps between reagents.\u003cbr\u003e Do not use the test beyond the expiration date.\u003cbr\u003e Keep out of reach of children.\u003cbr\u003e Do not use the test if the pouch is punctured or not well sealed.\u003cbr\u003e Discard after use. The test is single-use.\u003cbr\u003e Avoid contact of reagents A and B with eyes, sensitive mucous membranes, membranes, cuts, abrasions, etc. If these reagents come into contact with skin or eyes, rinse thoroughly with water.\u003cbr\u003e Do not eat, drink, or smoke in the area where samples are located and where the test will be performed.\u003cbr\u003e Protective gloves should be worn when handling the sample. Wash hands thoroughly after the procedure.\u003cbr\u003e The used device, swab, and extraction tube should be treated as infectious waste and therefore disposed of in biohazard containers.\u003cbr\u003e The results of this test should not be used to determine pharyngitis infections, as pharyngitis can be caused by organisms other than group A streptococcus. This test provides no information on pharyngitis other than that caused by type A streptococcal infection.\u003cbr\u003e A negative result may occur due to an insufficient amount of sample collected or if an insufficient amount of reagent A and B is added. If symptoms persist, always consult your doctor.\u003cbr\u003e Excess blood or mucus in the collected sample could interfere with the test's performance and could generate a false positive result. Do not touch the tongue, cheeks, teeth, or any bleeding areas of the mouth with the swab during the sample collection phase.\u003cbr\u003e Confirm test results with a diagnosis exclusively from a doctor after evaluating all clinical and laboratory results.\u003cbr\u003e The test should be performed by parents or another adult family member on all minors under 16 years of age.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eStorage\u003c\/b\u003e\u003cbr\u003e Store at 4-30 °C in the sealed package until the expiration date.\u003cbr\u003e Keep away from sunlight, moisture, and heat. Do not freeze.\u003cbr\u003e Preferably open the pouch just before performing the test.\u003cbr\u003e Validity of unopened packaging: 24 months.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e The kit contains:\u003cbr\u003e 1. individually sealed pouch containing: test device and desiccant pouch;\u003cbr\u003e 2. extraction tube;\u003cbr\u003e 3. sterile pharyngeal swab;\u003cbr\u003e 4. extraction reagent A (1 ml);\u003cbr\u003e 5. extraction reagent B (1 ml);\u003cbr\u003e 5. leaflet with instructions for use.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCode\u003c\/b\u003e 101129\u003c\/div\u003e","brand":"GAMMADIS FARMACEUTICI Srl","offers":[{"title":"Default Title","offer_id":45944255152395,"sku":"987479437","price":11.95,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_46e211d0-d9c9-467a-936f-50dcae2450cd.jpg?v=1727814197"},{"product_id":"wellion-luna-10-strips-strisce-per-misurazione-colesterolo","title":"WELLION LUNA 10 STRIPS CHOLESTEROL TEST STRIPS","description":"\u003ch1\u003eWellion\u003c\/h1\u003e \u003ch2\u003e Luna\u003c\/h2\u003e \u003cdiv align=\"justify\"\u003e\n\n\u003cb\u003e Description\u003c\/b\u003e\u003cbr\u003e Wellion LUNA test strips are high-tech products. The strips have been manufactured in several layers containing electrodes that have been placed using a sophisticated procedure. During the measurement, a certain amount of current is produced, which is calculated into a cholesterol result displayed on the screen. For cholesterol measurement, auto-coding technology facilitates the measurement. The end, where the blood is drawn into the reaction zone with the help of sip-in technology, has a sufficient distance from the meter to prevent contamination of the meter with blood. For use with the Wellion LUNA meter.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e \u003cbr\u003ePack of 10 pieces.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCode.\u003c\/b\u003e WELL610CHOL\u003c\/div\u003e","brand":"MED TRUST ITALIA Srl","offers":[{"title":"Default Title","offer_id":45944284938507,"sku":"925606840","price":24.92,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_91d5dab8-d32f-438f-a72a-cae118f3fd64.jpg?v=1727814545"},{"product_id":"borsa-prontex-diagnostic-bag-sterile-femminile-19120","title":"PRONTEX DIAGNOSTIC BAG STERILE FEMALE 19120","description":"\u003ch1\u003eDiagnostic \u003c\/h1\u003e \u003cb\u003eFEMALE BAG\u003c\/b\u003e\u003cbr\u003e\u003cbr\u003e Sterile bag with anatomical adhesive rim for collecting children's urine.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCode\u003c\/b\u003e 19120","brand":"SAFETY SpA","offers":[{"title":"Default Title","offer_id":45944319443211,"sku":"908893922","price":0.75,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_dbf2e4b1-10a3-4add-a7c4-c9bd64882565.jpg?v=1727814939"},{"product_id":"test-rapido-per-rilevazione-droghe-nellurina","title":"RAPID DRUG TEST FOR URINE","description":"\u003ch1\u003eRapid Urine Drug Test\u003c\/h1\u003e \u003cb\u003eURINE TEST\u003c\/b\u003e\u003cbr\u003e\u003cbr\u003e \u003cb\u003eIndications:\u003c\/b\u003e\u003cbr\u003e A rapid test for the qualitative detection of drugs in urine. This is a single-phase lateral flow immunoassay that works by detecting the presence of catabolites derived from the metabolism of these substances in the urine. Since it uses 6 to 10 different parameters (Multidrug), it can diagnose the use of almost all drugs of abuse (D.O.A.).\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFeatures:\u003c\/b\u003e\u003cbr\u003e The test is simple and very quick to use, requiring no diagnostic instruments.\u003cbr\u003e The parameters used are as follows: methadone, cocaine, cannabis, benzodiazepine, morphine, barbiturates, PCP, amphetamine, methamphetamine, tricyclics, opiates, ecstasy, buprenorphine.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCode\u003c\/b\u003e MB106ITP","brand":"DI.RA.LAB. Srl","offers":[{"title":"Default Title","offer_id":45944426004747,"sku":"911125363","price":15.37,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_6debd5ce-f4ee-479a-898f-b3350c4d9497.jpg?v=1727815898"},{"product_id":"screen-test-rapido-antigeni-helicobacter-pylori-feci-umane","title":"RAPID SCREEN TEST FOR HELICOBACTER PYLORI ANTIGENS IN HUMAN STOOL","description":"\u003ch1\u003eSCREEN\u003cbr\u003e CHECK TEST\u003c\/h1\u003e \u003cb\u003eH. Pylori Antigen\u003c\/b\u003e\u003cbr\u003e \u003cbr\u003e \u003cdiv align=\"justify\"\u003e\n\n\u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e CE 0123 In vitro diagnostic medical device. \u003cbr\u003e Rapid test for the qualitative detection of Helicobacter pylori (H. pylori) antigens in human faeces.\u003cbr\u003e For in-vitro self-diagnostic use only.\u003cbr\u003e \u003cbr\u003e \u003cb\u003ePrecautions\u003c\/b\u003e\u003cbr\u003e 1. For in-vitro self-diagnostic use only.\u003cbr\u003e 2. Do not eat, drink, or smoke in the area where samples or kits are handled.\u003cbr\u003e 3. Store in a dry place at 2-30°C (36-86°F), avoiding areas with excessive humidity. If the sealed packaging is damaged or open, please do not use the test.\u003cbr\u003e 4. Use a clean container to collect the faecal sample.\u003cbr\u003e 5. Carefully observe the indicated times.\u003cbr\u003e 6. Use the test only once.\u003cbr\u003e 7. Do not disassemble or touch the test window on the stand.\u003cbr\u003e 8. The kit must not be frozen or used beyond the expiry date printed on the packaging.\u003cbr\u003e 9. After use, all components should be discarded with normal household waste.\u003cbr\u003e 10. Keep out of reach of children.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eInstructions for use\u003c\/b\u003e\u003cbr\u003e 1. Wash hands with soap and rinse with clean water.\u003cbr\u003e 2. For faecal sample collection: The faecal sample should be collected on the faecal collection sheet or in a clean container. Please use the faecal collection sheet, avoiding sample contamination by taking due precautions to ensure that the sample or the side of the paper containing the sample does not come into contact with other contaminating objects, including bathroom products.\u003cbr\u003e 3. To analyse faecal samples: Unscrew the cap of the sample collection tube, then randomly pierce the collected sample with the applicator into the faecal sample at at least 3 different points. Do not shake the faecal sample. Screw the cap back on and secure it onto the collection tube, then shake the sample collection tube vigorously to mix the sample and the extraction buffer.\u003cbr\u003e 4. Bring the package to room temperature before opening. Remove the test device from the sealed package and use it as soon as possible. Best results are obtained if the test is performed immediately after opening the package.\u003cbr\u003e 5. Open the cap on the sample collection tube and break off the tip. Invert the tube and dispense 2 full drops of the extracted sample into the sample well (S) on the test device, then start the timer. Avoid trapping air bubbles in the sample well (S).\u003cbr\u003e 6. Read the results at 10 minutes. Do not read the results after 20 minutes.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eReading results\u003c\/b\u003e\u003cbr\u003e POSITIVE*: Two lines appear. Both the T (Test) and C (Control) lines appear. This result indicates the presence of H. pylori antigen in the faeces and a doctor should be consulted.\u003cbr\u003e NEGATIVE: A coloured line appears in the control region (C). No line appears in the test region (T). This result indicates that the presence of H. pylori antigen in the faeces could not be detected.\u003cbr\u003e INVALID: The control line does not appear. The most likely reasons for the control line not appearing are insufficient sample volume or incorrect procedural techniques. Review the procedure and repeat the test with a new kit. If the problem persists, stop using the kit immediately and contact your local distributor.\u003cbr\u003e *The colour intensity in the test region (T) varies depending on the concentration of H. pylori antigen present in the sample. Therefore, any shade of colour of the test line (T) should be considered positive.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eLimitations\u003c\/b\u003e\u003cbr\u003e 1. The H. pylori antigen (Faeces) test is for in-vitro diagnostic use only. The test should only be used for the detection of H. pylori antigens in faecal samples. This qualitative test does not allow for the determination of either the quantitative value or the growth rate of H. pylori antigen concentration.\u003cbr\u003e 2. The H. pylori antigen (Faeces) test will only indicate the presence of H. pylori in the sample and should not be used as the sole criterion to establish that H. pylori is the causative agent of peptic or duodenal ulcers.\u003cbr\u003e 3. As with all diagnostic tests, all results must be interpreted in conjunction with other clinical information available to the physician.\u003cbr\u003e 4. If the test result is negative and clinical symptoms persist, further testing using other clinical methods is recommended. A negative result does not in any way rule out the possibility of an H. pylori infection.\u003cbr\u003e 5. Following certain antibiotic treatments, the concentration of H. pylori antigens may fall below the minimum detection level of the test. Therefore, diagnosis during antibiotic treatment should be made with caution.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eStorage\u003c\/b\u003e\u003cbr\u003e The kit can be stored at room temperature or refrigerated (2-30°C).\u003cbr\u003e The test is stable until the expiry date printed on the sealed package.\u003cbr\u003e The test must remain in the sealed package until use.\u003cbr\u003e DO NOT FREEZE. Do not use beyond the expiry date. \u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Pack containing 1 piece.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eBIBLIOGRAPHY:\u003c\/u\u003e\u003cbr\u003e 1. Marshall, BJ, McGechie, DB, Rogers, PAR and Glancy, RG. Pyloric Campylobacter infection and gastroduodenal disease. Med. J. Australia. (1985), 149: 439-44.\u003cbr\u003e 2. Soll, AH. Pathogenesis of peptic ulcer and implications for therapy. New England J. Med. (1990), 322: 909-16.\u003cbr\u003e 3. Hazell, SL, et al. Campylobacter pylori is and gastritis I: Detection of urease as a marker of bacterial colonization and gastritis. Amer. J. Gastroenterology. (1987), 82(4): 292-96.\u003cbr\u003e 4. Cutler AF. Testing for Helicobacter pylori in clinical practice. Am j. Med. 1996; 100:35S-41S.\u003cbr\u003e 5. Anand BS, Raed AK, Malaty HM, et al. Loe point prevalence of peptic ulcer in normal individual with Helicobacter pylori infection. Am J Gastroenterol. 1996,91:1112-1115.\u003c\/div\u003e","brand":"SCREEN ITALIA Srl","offers":[{"title":"Default Title","offer_id":45944597840139,"sku":"926819172","price":10.93,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_28af5e2f-f947-47fd-b12a-6292d7398e3e.jpg?v=1727817587"},{"product_id":"screen-test-rapido-screen-test-celiachia-per-rilevazione-intolleranza-glutine-1-pezzo","title":"RAPID SCREEN TEST CELIAC DISEASE SCREEN TEST FOR GLUTEN INTOLERANCE 1 PIECE","description":"\u003ch2\u003eSCREEN CHECK TEST\u003c\/h2\u003e \u003ch1\u003eCeliac Disease Screen Test\u003c\/h1\u003e \u003cdiv align=\"justify\"\u003e \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e An immunochromatographic rapid test that can be used as an aid in the diagnosis of gluten intolerance. It detects IgA anti-transglutaminase (tTG) antibodies from a whole blood sample.\u003cbr\u003e If IgA anti-tTGA antibodies are present, they bind to anti-IgA antibodies (mouse IgG) labelled with colloidal gold and to tTG (derived from the lysis of red blood cells by the dilution buffer). The tTG binds this complex to the static protein line (test line) and produces a visible reddish line. The test also includes a control system consisting of a reference line.\u003cbr\u003e The test result must be confirmed by a doctor who can discuss the possibility of a gluten-free diet with the patient.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eHow to use\u003c\/b\u003e\u003cbr\u003e Before starting the test, bring the cassette and the sample dilution buffer to room temperature (15 °C to 27 °C). Open the container with the sample dilution buffer by removing the lid and place it vertically on the table.\u003cbr\u003e \u003cbr\u003e Unscrew the grey cap of the automatic lancet by twisting it until it loosens. Then, twist it at least two more times. Only then can it be removed; otherwise, its function is not guaranteed. The lancet can only be used once. Press the lancet with the round opening against the side of the clean fingertip and push the trigger.\u003cbr\u003e Open the plastic container and carefully remove the glass capillary tube. Squeeze a drop of blood from the fingertip. Hold the glass capillary tube horizontally in the drop of blood until the capillary tube is completely filled. Use the included plaster as needed.\u003cbr\u003e Place the filled glass capillary tube in the container with the sample dilution buffer and close tightly with the lid. Shake the container a few times until the blood in the capillary tube has completely mixed with the solution. Before removing the lid from the container, wait for the liquid to collect at the bottom of the container. Then open the container lid.\u003cbr\u003e Open the cassette's foil pouch just before use. Remove the test cassette and place it on a flat surface. With the pipette, draw a few drops of the diluted sample. Hold the pipette with the diluted sample vertically over the sample well (S) and pour exactly 5 drops into it. Ensure that no liquid is spilled onto the result window, marked with T and C. After applying the drops, do not touch or move the test cassette.\u003cbr\u003e Once the 5 drops have been added, read the result after 10-15 minutes. Low values may not be detected before 10 minutes have passed, and false positive results may occur after more than 15 minutes.\u003cbr\u003e \u003cbr\u003e \u003cu\u003eInterpretation of results\u003c\/u\u003e\u003cbr\u003e POSITIVE: a light or dark red line appears at the control line (C) and a light or dark red line appears at the test line (T).\u003cbr\u003e The test shows that IgA antibodies associated with gluten intolerance have been detected in the blood sample. The detection of these antibodies very likely indicates the presence of gluten intolerance. For a definitive diagnosis, consult your doctor.\u003cbr\u003e \u003cbr\u003e NEGATIVE: a light to dark red line appears at the control line (C) and no red line appears at the test line (T).\u003cbr\u003e The test shows that no IgA antibodies indicating gluten intolerance are detectable in the blood sample. Therefore, the presence of gluten intolerance can be virtually ruled out. In case of gastrointestinal discomfort or other symptoms, further diagnostic investigation by a doctor is necessary.\u003cbr\u003e \u003cbr\u003e INVALID: no red line appears at the control line (C) or only a red line appears at the test line (T).\u003cbr\u003e The test was not performed correctly and is invalid. Check that you have followed all instructions for use exactly. Perform a new test with a new blood sample.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e The test is for external use only.\u003cbr\u003e Do not ingest test components. Avoid skin and eye contact with the sample diluent buffer.\u003cbr\u003e Keep the test out of reach of children. \u003cbr\u003e The product can only be used until the expiry date printed on the product itself.\u003cbr\u003e If the instructions for use are not followed correctly and in detail, the test results may be inaccurate. The final diagnosis must be made by a doctor.\u003cbr\u003e Do not use the test if the packaging is damaged. Do not use damaged test components.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eStorage\u003c\/b\u003e\u003cbr\u003e Do not expose the test to direct sunlight or frost. Do not freeze. Store in a dry place at a temperature between 10 °C and 27 °C.\u003cbr\u003e Shelf life with intact packaging: 24 months.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e The kit contains:\u003cbr\u003e - 1 test cassette;\u003cbr\u003e - 1 pipette;\u003cbr\u003e - 1 glass capillary tube;\u003cbr\u003e - 1 bottle of solution with sample dilution buffer;\u003cbr\u003e - 1 sterile lancet;\u003cbr\u003e - 1 alcohol swab;\u003cbr\u003e - 1 plaster;\u003cbr\u003e - 1 instruction leaflet;\u003cbr\u003e - 1 translated information sheet.\u003c\/div\u003e","brand":"SCREEN ITALIA Srl","offers":[{"title":"Default Title","offer_id":45945310085387,"sku":"987315823","price":14.87,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_841582b9-f850-4c4b-b061-8b7119c2eef0.jpg?v=1727819578"},{"product_id":"test-antigenico-rapido-covid-19-autodiagnostico-determinazione-qualitativa-antigeni-sars-cov-2-in-tamponi-nasali-mediante-immunocromatografia","title":"COVID-19 RAPID ANTIGEN SELF-TEST QUALITATIVE DETECTION OF SARS-COV-2 ANTIGENS IN NASAL SWABS BY IMMUNOCHROMATOGRAPHY","description":"\u003ch1\u003eSARS-CoV-2 Antigen Rapid Test\u003c\/h1\u003e \u003cdiv align=\"justify\"\u003e \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e A rapid test intended for the qualitative detection of SARS-CoV-2 antigen (nucleocapsid protein) found in nasal cavity (anterior nasal) samples from individuals with suspected COVID-19 infection. The test kit is intended for self-testing or home testing.\u003cbr\u003e This test employs immune lateral chromatography technology. When the test sample contains SARS-CoV-2, the SARS-CoV-2 antigen will react with the antibody coated on the test line (T) causing a red band to appear in the test line area (T); when the SARS-CoV-2 content in the test sample is too low or non-existent, no red band appears in the test line area (T). Regardless of whether the test sample contains SARS-CoV-2, a red band will appear in the quality control line area (C), which is the basis for judging whether the test is effective.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eInstructions for use\u003c\/b\u003e\u003cbr\u003e 1. Use the test kit at room temperature (15°C-30°C). If the kit has been previously stored in a cool place (temperature below 15°C), equilibrate to 15°C-30°C for 30 minutes before testing.\u003cbr\u003e 2. Prepare a timer, tissues, hand sanitizer\/soap and warm water.\u003cbr\u003e 3. Wash hands thoroughly (at least 20 seconds) with soap and warm water\/hand sanitizer. Then dry hands.\u003cbr\u003e 4. Check the components in the box and ensure there is no damage or breakage.\u003cbr\u003e Sample collection:\u003cbr\u003e 1. Take out the sample extraction tube; unscrew the cap of the tube.\u003cbr\u003e 2. Place the extraction tube on the stand (attached to the box) to prevent liquid spills.\u003cbr\u003e 3. Tear the swab package from the stick end and take out the swab.\u003cbr\u003e 4. Insert the soft head of the swab into the nostril less than 1 inch; gently rotate the swab against the nasal wall with moderate force at least five times; use the same swab to repeat the collection procedure in the other nostril.\u003cbr\u003e Sample processing:\u003cbr\u003e 1. Take out the extraction tube, immerse the soft head of the swab in the extraction solution and submerge it in the liquid.\u003cbr\u003e 2. Firmly press the soft head of the swab against the inner wall of the extraction tube and rotate the swab clockwise or anti-clockwise about 10 times.\u003cbr\u003e 3. Push the swab head along the inner wall of the sample extraction tube below the liquid in the tube as much as possible, then remove the swab.\u003cbr\u003e 4. Tighten the tube cap for standby.\u003cbr\u003e Sample testing:\u003cbr\u003e 1. Tear open the aluminum foil pouch, take out the test card and place it horizontally on the test bench.\u003cbr\u003e 2. Disconnect the cap of the sample addition hole of the extraction tube.\u003cbr\u003e 3. Gently squeeze the extraction tube and drop 2 drops of liquid into the sample well of the test card.\u003cbr\u003e 4. Start timing, read the test results at 15 minutes. Do not read before 15 minutes or after 30 minutes.\u003cbr\u003e 5. After the test is completed, place all kit materials in the biohazard waste bag and dispose of them according to local biohazard waste disposal policy.\u003cbr\u003e 6. Rinse hands thoroughly for at least 20 seconds with soap and warm water\/hand sanitizer.\u003cbr\u003e Negative: The quality control line (C line) appears as a red band, while the test line (T line) does not appear as a red band.\u003cbr\u003e Positive: Both the quality control line (C line) and the test line (T line) appear as red bands.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e 1. For in vitro diagnostic use only.\u003cbr\u003e 2. To be used with nasal cavity (anterior nasal) swab samples.\u003cbr\u003e 3. For the detection of SARS-CoV-2 proteins only, not for detecting other viruses or pathogens.\u003cbr\u003e 4. Individuals under 18 years of age must be tested with the assistance of a legal guardian or authorized person.\u003cbr\u003e 5. Keep the test kit or kit components out of reach of children and pets before and after use.\u003cbr\u003e 6. The test card package contains a desiccant, do not eat.\u003cbr\u003e 7. The sample extraction solution in the extraction tube contains chemical components. Direct contact should be avoided and eating is prohibited. If the solution comes into contact with skin, mucous membranes or eyes, rinse with plenty of water. Please contact your family doctor or a professional or seek medical advice if necessary.\u003cbr\u003e 8. The use of gloves and other protective equipment is recommended when performing tests.\u003cbr\u003e 9. Test kits must be stored according to the storage conditions required in the instructions for use. It is forbidden to use a test kit that has not been stored as required.\u003cbr\u003e 10. Do not use the test kit beyond the expiration date.\u003cbr\u003e 11. Do not use kit components that have been opened or altered.\u003cbr\u003e 12. Leave the test card sealed in the aluminum foil pouch until just before use. Do not use if the pouch is damaged or opened.\u003cbr\u003e 13. Disposable swabs are sterile products. Do not use if the swab package is damaged or opened.\u003cbr\u003e 14. Swab use must strictly follow the instructions for use; otherwise, it may cause nasal cavity bleeding, swab breakage and retention, and other risks.\u003cbr\u003e 15. Do not immerse the swab in extraction solution or other liquid before collecting the sample with disposable swabs.\u003cbr\u003e 16. Do not touch the soft tip of the swab when handling the swab sample.\u003cbr\u003e 17. Proper sample collection and handling are crucial for accurate results.\u003cbr\u003e 18. Do not mix components from different kit lots.\u003cbr\u003e 19. All kit components are single-use items. Do not use with multiple samples. Do not reuse the test kit or used kit components.\u003cbr\u003e 20. Before deciding to implement relevant therapeutic or management decisions, it is recommended to communicate with family doctors or professionals. Do not take medicine privately or take any action that could endanger yourself.\u003cbr\u003e 21. Used test components and samples can be placed in plastic bags along with normal household waste. If the test result is positive, carefully dispose of waste components and relevant samples and thoroughly clean and disinfect the work surface to ensure hygiene. If there are special waste requirements in local laws and regulations, they must be strictly observed.\u003cbr\u003e 22. Do not eat, drink or smoke in the area where samples or test kits are handled.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eStorage\u003c\/b\u003e\u003cbr\u003e Store between 2°C and 30°C, in a dry place away from direct sunlight (do not freeze the kit or its components).\u003cbr\u003e Shelf life unopened: 12 months.\u003cbr\u003e Shelf life after opening: 60 minutes.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Main kit components:\u003cbr\u003e - Test device.\u003cbr\u003e - Extraction tube.\u003cbr\u003e - Disposable swab.\u003cbr\u003e - Biohazard waste bag.\u003cbr\u003e - Instructions for use. \u003c\/div\u003e","brand":"DIDOFA' Srl","offers":[{"title":"Default Title","offer_id":45945462096139,"sku":"983776713","price":1.56,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_b3ab457c-5a5f-40e6-b482-555ea9839be9.jpg?v=1727819985"},{"product_id":"borsa-prontex-diagnostic-bag-sterile-maschile","title":"PRONTEX DIAGNOSTIC MALE STERILE BAG","description":"\u003ch1\u003eDiagnostic \u003c\/h1\u003e \u003cb\u003eMALE URINE COLLECTION BAG\u003c\/b\u003e\u003cbr\u003e\u003cbr\u003e Sterile bag with an anatomical adhesive border for collecting urine from children.\u003cbr\u003e\u003cbr\u003e \u003cb\u003eCode\u003c\/b\u003e 19140","brand":"SAFETY SpA","offers":[{"title":"Default Title","offer_id":45945977569547,"sku":"908893946","price":0.75,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_83f500dc-ee2a-41cb-a4f6-3cfdc9a3b3f4.jpg?v=1727822394"},{"product_id":"screen-alcol-test-saliva","title":"SALIVA ALCOHOL TEST SCREEN","description":"\u003ch1\u003eSCREEN\u003cbr\u003e ALCOHOL TEST\u003c\/h1\u003e \u003cdiv align=\"justify\"\u003e\n\n\u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e Detects the presence of alcohol in the body via saliva.\u003cbr\u003e Disposable breathalyzer that measures the concentration of alcohol in the blood.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eHow to use\u003c\/b\u003e\u003cbr\u003e Before performing the test, bring it to a temperature between 15°C and 30°C.\u003cbr\u003e Insert the plastic stick into your mouth with the swab end for 10 seconds, wait 2 minutes to see the color of the swab.\u003cbr\u003e If alcohol is present in the body, the test swab will change color. Compare the color of the swab with the results scale on the back of the package.\u003cbr\u003e Detected gradients: 0.00 g\/l – 0.20 g\/l – 0.50 g\/l – 0.80 g\/l – 1.50 g\/l.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e Keep out of reach of children. Do not dispose of the container in the environment.\u003cbr\u003e Product not intended for medical or diagnostic use.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eStorage\u003c\/b\u003e\u003cbr\u003e Store at temperatures between 2°C and 30°C.\u003cbr\u003e Shelf life of unopened package: 18 months.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Pack containing 1 disposable test.\u003cbr\u003e\n\n\u003c\/div\u003e","brand":"SCREEN ITALIA Srl","offers":[{"title":"Default Title","offer_id":45946122797323,"sku":"912400696","price":1.31,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_7e2be888-9f20-464d-b7ad-293c1c5a2114.jpg?v=1727823723"},{"product_id":"provetta-conica-per-urina-da-12ml-pharmamentis","title":"PHARMAMENTIS 12ML CONICAL URINE TUBE","description":"\u003ch1\u003eCONICAL URINE TUBE\u003c\/h1\u003e \u003cdiv align=\"justify\"\u003e \u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e Class A in vitro diagnostic medical device.\u003cbr\u003e Conical urine tube made of polypropylene with a white cap. Product intended exclusively for the collection and transport of biological samples for laboratory analysis, in the case of urine tests.\u003cbr\u003e Beta-ray sterilized.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eComponents\u003c\/b\u003e\u003cbr\u003e Container: polypropylene.\u003cbr\u003e Cap: polyethylene.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e Do not place near flames or sources of ignition.\u003cbr\u003e Do not discard the product into the environment as it is not biodegradable.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eStorage\u003c\/b\u003e\u003cbr\u003e Store at room temperature in a dry place, away from heat sources.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Capacity: 12 ml\u003c\/div\u003e","brand":"V.I.M. Srl","offers":[{"title":"Default Title","offer_id":45946350862603,"sku":"985725997","price":0.75,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_20c6efd1-9a3b-4a91-9c9e-b8f8f81ba242.jpg?v=1727824983"},{"product_id":"strisce-misurazione-glicemia-glucomen-areo-sensor-50-pezzi","title":"GLUCOMEN AREO SENSOR BLOOD GLUCOSE TEST STRIPS 50 PIECES","description":"\u003ch1\u003eGlucoMen\u003cbr\u003e areo \u003ci\u003eSensor\u003c\/i\u003e\n\u003c\/h1\u003e \u003cdiv align=\"justify\"\u003e\n\u003cb\u003eDescription\u003c\/b\u003e\u003cbr\u003e In vitro diagnostic medical device.\u003cbr\u003e Sensors for the quantitative determination of glucose levels in fresh capillary whole blood; they are to be used exclusively with the GlucoMen areo 2K instrument.\u003cbr\u003e The sensors are designed for monitoring and self-testing of blood glucose levels in people with diabetes mellitus; they can also be used in hospital settings by medical and healthcare professionals.\u003cbr\u003e They are not intended for use in the diagnosis or screening of diabetes or for use in neonates.\u003cbr\u003e Do not change your treatment based on test results without first consulting your doctor or healthcare professional.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eGeneral characteristics\u003c\/b\u003e\u003cbr\u003e \u003ctable border=\"1cellspacing=0cellpadding=1\" width=\"500\"\u003e \u003ctr\u003e\n\u003ctd\u003e\u003cb\u003eBlood Glucose Measurement\u003c\/b\u003e\u003c\/td\u003e\n\u003ctd align=\"center\"\u003especificity for beta-D-glucose in blood\u003c\/td\u003e\n\u003c\/tr\u003e \u003ctr\u003e\n\u003ctd\u003e\u003cb\u003eEnzymatic composition (per cm\u003csup\u003e2\u003c\/sup\u003e) of a test strip for blood glucose measurement\u003c\/b\u003e\u003c\/td\u003e\n\u003ctd align=\"Center\"\u003e- glucose oxidase (from \u003ci\u003eAspergillus niger\u003c\/i\u003e), 3.5%\u003cbr\u003e - mediator: hexacyanoferrate (III) ion, 17.5%\u003cbr\u003e - non-reactive substances, 79%\u003c\/td\u003e\n\u003c\/tr\u003e \u003ctr\u003e\u003ctd colspan=\"2\"\u003e\u003cb\u003eUnit of measurement\u003c\/b\u003e\u003c\/td\u003e\u003c\/tr\u003e \u003ctr\u003e\n\u003ctd\u003eGlucose\u003c\/td\u003e\n\u003ctd align=\"Center\"\u003emg\/dL (not modifiable)\u003c\/td\u003e\n\u003c\/tr\u003e \u003ctr\u003e\u003ctd colspan=\"2\"\u003e\u003cb\u003eMeasurement range\u003c\/b\u003e\u003c\/td\u003e\u003c\/tr\u003e \u003ctr\u003e\n\u003ctd\u003eGlucose\u003c\/td\u003e\n\u003ctd align=\"Center\"\u003e20-600 mg\/dL\u003c\/td\u003e\n\u003c\/tr\u003e \u003ctr\u003e\u003ctd colspan=\"2\"\u003e\u003cb\u003eResponse time\u003c\/b\u003e\u003c\/td\u003e\u003c\/tr\u003e \u003ctr\u003e\n\u003ctd\u003eGlucose\u003c\/td\u003e\n\u003ctd align=\"Center\"\u003e5 seconds\u003c\/td\u003e\n\u003c\/tr\u003e \u003ctr\u003e\u003ctd colspan=\"2\"\u003e\u003cb\u003eSample volume\u003c\/b\u003e\u003c\/td\u003e\u003c\/tr\u003e \u003ctr\u003e\n\u003ctd\u003eGlucose\u003c\/td\u003e\n\u003ctd align=\"Center\"\u003e0.5 microL\u003c\/td\u003e\n\u003c\/tr\u003e \u003ctr\u003e\u003ctd colspan=\"2\"\u003e\u003cb\u003eHematocrit acceptability range\u003c\/b\u003e\u003c\/td\u003e\u003c\/tr\u003e \u003ctr\u003e\n\u003ctd\u003eGlucose\u003c\/td\u003e\n\u003ctd align=\"Center\"\u003eautomatically corrects the measurement based on hematocrit (10-70%)\u003c\/td\u003e\n\u003c\/tr\u003e \u003ctr\u003e\n\u003ctd\u003e\u003cb\u003eCorrelation\u003c\/b\u003e\u003c\/td\u003e\n\u003ctd align=\"Center\"\u003eplasma equivalent\u003c\/td\u003e\n\u003c\/tr\u003e \u003ctr\u003e\n\u003ctd\u003e\u003cb\u003eSample\u003c\/b\u003e\u003c\/td\u003e\n\u003ctd align=\"Center\"\u003efresh capillary whole blood\u003c\/td\u003e\n\u003c\/tr\u003e \u003ctr\u003e\n\u003ctd\u003e\u003cb\u003eSensor coding\u003c\/b\u003e\u003c\/td\u003e\n\u003ctd align=\"Center\"\u003eauto-coding\u003c\/td\u003e\n\u003c\/tr\u003e \u003ctr\u003e\n\u003ctd\u003e\u003cb\u003eHygiene\u003c\/b\u003e\u003c\/td\u003e\n\u003ctd align=\"Center\"\u003eautomatic test strip ejection via dedicated eject button\u003c\/td\u003e\n\u003c\/tr\u003e \u003ctr\u003e\n\u003ctd\u003e\u003cb\u003eSampling\u003c\/b\u003e\u003c\/td\u003e\n\u003ctd align=\"Center\"\u003eautomatic blood sample aspiration by capillarity\u003c\/td\u003e\n\u003c\/tr\u003e \u003ctr\u003e\n\u003ctd\u003e\u003cb\u003eUse of alternative sites (AST)\u003c\/b\u003e\u003c\/td\u003e\n\u003ctd align=\"Center\"\u003eallowed (palm of hand and forearm)\u003c\/td\u003e\n\u003c\/tr\u003e \u003ctr\u003e\n\u003ctd\u003e\u003cb\u003eOperating environment\u003c\/b\u003e\u003c\/td\u003e\n\u003ctd align=\"Center\"\u003etemperature range: 5-45°C\u003cbr\u003e humidity: 20%-90% (non-condensing)\u003c\/td\u003e\n\u003c\/tr\u003e \u003c\/table\u003e \u003cbr\u003e \u003cb\u003eInstructions for use\u003c\/b\u003e\u003cbr\u003e 1. Insert a new GlucoMen areo Sensor (white color) into the sensor insertion slot. The drop symbol will start flashing on the display and the glucose symbol Glu will appear in the bottom left corner. If nothing appears on the display, remove the sensor, reinsert it into the slot, and wait for the drop symbol to start flashing.\u003cbr\u003e For information on how to use the lancing device, please read its instructions for use.\u003cbr\u003e 2. Hold the end of the sensor in contact with the blood drop until the control window fills. A beep will then sound (if enabled) and the display will show a countdown.\u003cbr\u003e 3. Read the test results. A beep will announce the appearance of the test result on the screen with the glucose symbol Glu.\u003cbr\u003e 4. To remove the sensor, press the eject button. The device will turn off.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eWarnings\u003c\/b\u003e\u003cbr\u003e Keep the instrument, sensors, and other components out of reach and sight of children. Small parts can pose a choking hazard.\u003cbr\u003e Handle the vial and sensors with clean, dry hands.\u003cbr\u003e Dispose of the vial and used sensors in accordance with local regulations.\u003cbr\u003e Handling blood can be dangerous: exercise extreme caution when handling blood, sensors, lancets, and the instrument.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eStorage\u003c\/b\u003e\u003cbr\u003e Store the sensor vial in a dry place, at a temperature of 4-30°C. Do not freeze. Avoid heat and direct sunlight.\u003cbr\u003e Store all unused sensors in their original vial and, after removing one, close the cap tightly to preserve their quality. Do not transfer sensors to other containers.\u003cbr\u003e Do not use sensors beyond their expiration date.\u003cbr\u003e Do not use sensors more than 12 months after first opening their vial. It is recommended to write the disposal date (first opening date + 12 months) on the label.\u003cbr\u003e Sealed strips have a shelf life of 24 months from the manufacturing date.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eFormat\u003c\/b\u003e\u003cbr\u003e Pack of 50 sensors.\u003cbr\u003e \u003cbr\u003e \u003cb\u003eCod.\u003c\/b\u003e 49198\u003c\/div\u003e","brand":"A.MENARINI DIAGNOSTICS","offers":[{"title":"Default Title","offer_id":45946601242891,"sku":"939605046","price":25.31,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/4683\/0859\/files\/GetDoc_4690e09a-e609-4c44-938b-b0fbd8a546df.jpg?v=1727828036"},{"product_id":"cartina-rilevatrice-ph-15-pezzi","title":"PH INDICATOR PAPER 15 PIECES","description":"\u003ch1\u003ePH TEST STRIPS 15 PIECES\u003c\/h1\u003e","brand":"NAMED Srl","offers":[{"title":"Default Title","offer_id":45946830160139,"sku":"976102210","price":6.05,"currency_code":"EUR","in_stock":true}]}],"url":"https:\/\/farmaonline24.it\/en\/collections\/analisi.oembed?page=5","provider":"FarmaOnline24","version":"1.0","type":"link"}