Trudell Medical International AeroEclipse XL Manuel De L'utilisateur page 11

†
Neodisher Mediclean forte 0.5% and Neodisher
equipment used for thermal disinfection should conform to DIN EN ISO 15883.
5.1.2 RECOMMENDED PROCEDURE: MANUAL CLEANING AND DISINFECTION
CAUTION: The AEROECLIPSE* XL BAN (and its accessories) are not suitable for treatment with
disinfectants based on quaternary ammonium compounds. Quaternary ammonium compounds tend to
become concentrated in plastic materials, which can cause incompatibility reactions in patients.
approximately 50°C warm water and clean thoroughly with a brush. This process should take approximately
5 minutes.
for 15 minutes.
and leave to air dry thoroughly on a clean, dry and absorbent surface.
5.2 STERILIZATION
Your nebulizer (excluding tubing) may be sterilized using the following validated procedures. If another
procedure is used, its effectiveness must be validated. Hospital hygiene standards should be followed.
disinfected following instructions in Section 5.1.
(disposable sterilization packaging) conforming to DIN EN ISO 11607. Packaging size should be no smaller
than 70 mm x 120 mm.
NOTE: When placing the nebulizer components in the sterilization packaging, the
portion of the NEBULIZER TOP
where it can become bent (as shown).
5.2.1 RECOMMENDED PROCEDURE: STEAM STERILIZATION
Autoclave the reusable AEROECLIPSE* XL BAN following the autoclave manufacturer's instructions
preferably with fractionated pre-vacuum – in accordance with DIN EN 285 or DIN EN 13060 (type B).
†
Z for neutralization (Dr. Weigert, Hamburg). The
†
basic 4% disinfectant (Bode Chemie, Hamburg).
should be positioned in the packaging so it is not bent or pressed into corners
†
EndoCleaner 0.5% and
†
EndoCleaner 0.5% cleaning agent in
WHITE CYLINDER
9
†
basic 4%
EN