WATER
Mefar 2000

Medical device class IIa.
It is intended to be used for the administration of aerosol drugs to the patient. The administration must be the subject of a prescription that defines the type of drug, the doses to be administered and the duration of treatment.

Mode of use
To avoid any risk of microbial contamination, the components must be cleaned and disinfected, after each therapy and before use, following carefully the instructions listed.
Cleaning
The amp, the mouthpiece and the nasal with the fitting, must be washed with hot water using a little non-abrasive detergent and rinse under running water. When all parts have been cleaned can be dried with a soft cloth or with a hair dryer so they can be rested.
Disinfection
The amp, the mouthpiece, the nasal with the fitting and the tube terminal, after being washed, can be immersed in a cold disinfectant solution (e.g. a 5.25% solution of hypochlorite sodium), following the instructions indicated by the manufacturer (be careful to consult the warnings verifying that the disinfectant solution is compatible with the material of which the kit is constituted). it is possible to disinfect the components of the kit excluding the tube terminal by boiling them in water for 10 min.
Sterilization
The sterilization . possible for the components of the kit except for the tube terminal in 121°C autoclave for a time of 15 min. (preferably not exceed 30 min.).

Technical specifications:
Minimum feeding pressure: 1.5 bar (150 kPa)
Maximum feeding pressure: 3 bars (300 kPa)
Minimum pressure air flow: 7 l/min
Maximum pressure air flow: 15 l/min
Drug delivery at minimum pressure: 0.20 ml/min
Drug 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
Ampolla, mouthpiece, and nasal (with its connection): polycarbonate.
Terminal tube aerosol: PVC.
There is no natural latex.
Phthalates are not detected.

Format
1 piece.

Cod. 471130