Before initial use, the product should be kept in its original packaging. GCE
recommends the use of the original packaging (including internal sealing
bag and caps) if the product is withdrawn from operation (for transport, stor-
age).
Statutory laws, rules, and regulations for medical gases, accident preven-
EN
tion, and environmental protection must be observed.
OPERATING CONDITIONS
In case of storage at a temperature below +5°C, do not operate the prod-
uct until it has been allowed to increase its temperature to a minimum of
+5°C.
4. PERSONNEL INSTRUCTIONS AND TRAINING
According to Medical Devices Directive 93/42/EEC, the product provider
must ensure that all personnel handling the product are provided with the
operating instructions & performance data and are fully trained to carry out
that operation. Trainees need to be supervised by an experienced person.
Do not use the device without being trained. Training can be only done by
a person with an appropriate education, experience and knowledge that
has been also trained by the manufacturer.
For further information about training programs, please contact GCE.
5. PRODUCT DESCRIPTION
Fig. 1: Complex version of panel for exposed mounting
The inlet connection port (A) is intended for connection of a source of medi-
cal gas (e.g., pressure regulator, pressure regulator integrated with cylinder
valve, etc.) via a flexible hose. The gas may come to the panel directly or
through the source cylinder switch (B).
The outlet from the panel is realized by the quick couplers (C) or by directly
connected MediFlow® selector outlet (G). The gas pressure indicator (D) is
an indicator of internal panel pressure. Gas from the medical gas pipeline
system is entering through the inlet connector (A).
It is possible to connect other parts of ambulance gas supply system via the
flexible hoses connected to the outlet (E).
+5/+40°C
10/100%
600/1200 mbar
4/191
STORAGE AND TRANSPORT
-30/+70°C
10/100%
600/1200 mbar