You will not be allowed to compare more than 4 products at a time
View compareDescription
SCREEN
Strep A
Description
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.
When the sample is added to the dedicated well, capillary action causes the sample to migrate through the membrane. When the levels of Strep A antigen in the samples are at 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.
For in vitro self-testing.
Instructions for use
Sample collection and preparation
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.
The test should ideally be performed immediately after sample collection.
Performing the test
Bring the device and extraction reagents to room temperature (10-30 °C) before performing the test.
Add 4 drops of extraction reagent A and 4 drops of reagent B to the respective extraction tube and mix thoroughly.
Place the extraction swab in the tube. Agitate 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. Discard the used swab.
Remove the test from the sealed foil pouch, tearing at the notch, and place the test on a clean, dry, flat surface.
Add 3 drops of extracted sample into the sample well on the test cassette.
Wait 10 minutes and read the results. Do not read the results after 15 minutes.
Interpretation of results
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 recommended to consult your doctor.
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.
INVALID: No colored line appears, or only a 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.
Warnings
For in vitro self-testing use only.
Do not ingest.
Do not swap caps between reagents.
Do not use the test beyond the expiry date.
Keep out of reach of children.
Do not use the test if the packaging is perforated or not well sealed.
The test is single-use: discard after use.
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.
Do not eat, drink, or smoke in the area where samples are handled and where the test is performed.
The used device, swab, and extraction tube should be treated as infectious waste and therefore disposed of in biohazard waste containers.
Storage
Store at 4-30 °C. Keep away from sunlight, moisture, and heat. Do not freeze.
Shelf life unopened: 24 months.
Format
The kit contains:
- 1 sealed pouch (containing a test device and a desiccant sachet);
- 1 extraction tube;
- 1 sterile throat swab;
- extraction reagents A and B;
- instruction leaflet.
Code W039P0001
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.
When the sample is added to the dedicated well, capillary action causes the sample to migrate through the membrane. When the levels of Strep A antigen in the samples are at 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.
For in vitro self-testing.
Instructions for use
Sample collection and preparation
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.
The test should ideally be performed immediately after sample collection.
Performing the test
Bring the device and extraction reagents to room temperature (10-30 °C) before performing the test.
Add 4 drops of extraction reagent A and 4 drops of reagent B to the respective extraction tube and mix thoroughly.
Place the extraction swab in the tube. Agitate 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. Discard the used swab.
Remove the test from the sealed foil pouch, tearing at the notch, and place the test on a clean, dry, flat surface.
Add 3 drops of extracted sample into the sample well on the test cassette.
Wait 10 minutes and read the results. Do not read the results after 15 minutes.
Interpretation of results
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 recommended to consult your doctor.
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.
INVALID: No colored line appears, or only a 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.
Warnings
For in vitro self-testing use only.
Do not ingest.
Do not swap caps between reagents.
Do not use the test beyond the expiry date.
Keep out of reach of children.
Do not use the test if the packaging is perforated or not well sealed.
The test is single-use: discard after use.
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.
Do not eat, drink, or smoke in the area where samples are handled and where the test is performed.
The used device, swab, and extraction tube should be treated as infectious waste and therefore disposed of in biohazard waste containers.
Storage
Store at 4-30 °C. Keep away from sunlight, moisture, and heat. Do not freeze.
Shelf life unopened: 24 months.
Format
The kit contains:
- 1 sealed pouch (containing a test device and a desiccant sachet);
- 1 extraction tube;
- 1 sterile throat swab;
- extraction reagents A and B;
- instruction leaflet.
Code W039P0001



