Product And Function Description - GCE MEDIEJECT II Mode D'emploi

OPERATING CONDITIONS
EN
Before initial use the product shall be kept in its original packaging.
GCE recommends use of the original packaging (including internal sealing
bag and caps) if the product is withdraw from operation (for transport and
storage). Statutory laws, rules and regulations for medical gases, accident
prevention and environmental protection must be observed.
4. PERSONNEL INSTRUCTIONS
The Medical Devices Directive 93/42/EEC states that product provider
must ensure that all personnel handling the product are provided with the
operating instructions & performance data.
Do not use the product without properly familiarization of the product
and its safe operation as defined in this Instruction for use. Ensure user
is aware of particular information and knowledge required for the gas
in use.

5. PRODUCT AND FUNCTION DESCRIPTION

MediEject II suction ejector includes 3 basic variants:
• MediEject II with probe*
• MediEject II T-slide
•
•
• MediEject II Rail clamp*
•
•
* according to national standards
It mainly consists of a probe connector (gas source side) (A), an integrated
push-pull on/off valve and control handwheel (B), a vacuum indicator (C), a
hose nipple (patient side) (D) and silencer (E).
A. Probe Connector (medical pipeline or mobile gas source side)
The product is fitted to the medical gas pipeline system or mobile gas
source by a oxygen/air type male probe. The probe is directly mounted on
the ejector or on the hose via rail mounting system.
-10/+40 °C
10/70 %
950/1100 mbar
with NIST
with HOSE and probe*
with NIST
with HOSE and probe*
STORAGE AND TRANSPORT
CONDITIONS
-20/+60 °C
10/100 %
600/1200 mbar
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