FLAEM Baby Mask Mode D'emploi page 10

towel. Alternatively, dry them with a jet of hot air (for example, from a hair dryer).
STERILIZATION: The accessories that can be sterilized are (M0,M1,M2,R)
Device: Fractionated vacuum overpressure steam steriliser in accordance with EN 13060.
Implementation: Wrap every single part to be treated with a sterile barrier system or
packaging in accordance with Norm EN 11607. Place the packed components in the steam
steriliser. Run the sterilisation cycle according to the operating instructions of the device by
selecting a temperature of 134°C and a time of 10 minutes first.
Storage: Store the sterilised parts as per the instructions for use of either the sterile barrier
system or packaging.
The sterilisation procedure is validated in its conformity to ISO 17665-1.
At the end of each use store the accessories in a dry place away from dust.
INTERACTIONS
The materials used that come into contact with medications have been tested with a wide
range of medications. However, due to the variety and continuous evolution of medication,
the possibility of a chemical interaction cannot be excluded. We recommend that once the
medication has been opened you should use it as soon as possible and avoid prolonged
contact of the medication with the nebulizer.
Use only Flaem originals accessories.
MODEL: M0= B014 - M1=B015 - M2=B016 - R=B002 The applied parts of type BF are: (M0, M1, M2)
SYMBOLS
EC Marking medical ref. Dir 93/42 EEC
and subsequent updates
In compliance with: European Standard
EN 10993-1 ''Biological Evaluation
of medical devices'' and European
Directive 93/42/EEC "Medical Devices. "
Phthalate-free. In compliance with:
Reg. (EC) no. 1907/2006
PACKAGING DISPOSAL
04 Product packaging bag and Tube packaging bag
LDPE
Check the instructions for use
Manufacturer
LOT
Lot Number
8