AMPOULE
Mefar2000

Class IIa medical device.
Intended for use in administering aerosolized medication to patients. Administration must be subject to a medical prescription defining the type of medication, the doses to be administered, and the duration of treatment.

Instructions for use
To avoid the risk of microbial contamination, components must be cleaned and disinfected after each therapy and before use, carefully following the instructions listed.
Cleaning
The ampoule, mouthpiece, and nasal piece with connector must be washed with hot water using a little non-abrasive detergent and rinsed under running water. Once all parts have been cleaned, they can be dried with a soft cloth or a hairdryer, then stored.
Disinfection
The ampoule, mouthpiece, nasal piece with connector, and the end of the tube, after being washed, can be immersed in a cold disinfectant solution (such as a 5.25% sodium hypochlorite solution), following the manufacturer's instructions (attention: consult the warnings to ensure that the disinfectant solution is compatible with the material of which the kit is made). It is possible to disinfect the components of the kit, excluding the end of the tube, by boiling them in water for 10 min.
Sterilization
Sterilization is possible for the kit components, with the exception of the end of the tube, in an autoclave at 121°C for 15 min. (preferably not exceeding 30 min.).

Technical specifications:
Minimum supply pressure: 1.5 bar (150 kPa)
Maximum supply pressure: 3 bar (300 kPa)
Air flow at minimum pressure: 7 l/min
Air flow at maximum pressure: 15 l/min
Medication delivery at minimum pressure: 0.20 ml/min
Medication delivery at maximum pressure: 0.45 ml/min
MMAD at minimum pressure: 2.5 µm
MMAD at maximum pressure: 1.9 µm
Maximum capacity: 8 ml

Components
Ampoule, mouthpiece, and nasal piece (with relevant connector): polycarbonate.
Aerosol tube end: PVC.
No natural latex detected.
No phthalates detected.

Format
1 piece.

Code 471130