IV. 6. Accessories
The accessories used with OSIRIS 2 must:
• be oxygen compatible,
• be biocompatibles,
• conform to the general requirements of EN 60601-1 and of directive 93/42/CEE,
• and not be antistatic or conductors of electricity.
The use of accessories which do not conform to the above descriptions releases Air Liquide Medical Systems from
any responsibility in the event of an incident.
Accessories referenced by Air Liquide Medical Systems or included in the batch of accessories delivered with the
equipment conform to these requirements.
Electromedical apparatus associated or used with OSIRIS 2 must conform to the requirements of the directive 93/42/
CEE (medical equipment).
The apparatus is delivered with:
1 transportation case
3 single-use patient circuits
1 NiMH battery pack
1 mains/charger adapter
1 adult mask
1 child's mask
1 3 m O
tube with fixed connector
2
Optional accessories:
1 stand for OSIRIS 2
1 autoclavable patient circuit
1 autoclavable expiratory valve
20 single-use patient circuits
1 articulated arm, chrome
1 wheeled base
1 Ambulance compatible wall-support
IV. 7. Waste disposal
All waste products coming from OSIRIS 2 (the patient circuit, etc.) must be disposed of according to the appropriate
procedures of the hospital.
IV. 8. Disposal of equipment
To protect the environment, all equipment disposal must be made according to the appropriate procedures of the hospital.
Besides, traceability being imposed by the C marking, it is obligatory to communicate the disposed equipment's serial
number to Air Liquide Medical Systems technical department.
KF006500
KY564600
KY564800
KM030000
KM030100
BF030200
KA004600
KG018700
KY133900
KG020300
KB005200
KB005000
KY581900
YL024400 - V 2.1 - 10/2012
EN
17