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ENGLISH
INSTRUCTION FOR USE: AMBULANCE PANEL II
1. FOREWORD
GCE Ambulance Panels are medical devices classified as class IIb accord-
ing to the Medical Device Directive 93/42/EEC.
Their Compliance with essential requirements of 93/42/EEC Medical De-
vice Directive is based upon EN ISO 1789 standard.

2. INTENDED USE

Ambulance panels are designed for use as an integral part of ambulances.
When connected to the source of medical gas (e.g. regulator, pressure
regulator integrated with cylinder valve) then can be used as a terminal unit
and allow the connection and gas supply of different medical devices, e.g.
flowmeter, resuscitator, ventilator, suction ejector. They are intended for ad-
ministration of the following medical gases in the treatment, management,
diagnostic, evaluation and care of the patient:
oxygen
air for breathing
nitrous oxide
specified mixtures of the gases listed
vacuum
Ambulance panels are not intended for the driving of surgical tools.
Working pressure of Ambulance Panel is from 4 to 5 bar for medical gases
and ≤ 40 kPa (expressed as absolute pressure) for vacuum.
3. OPERATIONAL, TRANSPORT AND STORAGE
SAFETY REQUIREMENTS
Keep the product and its associated equipment away from:
• Heat sources and sun light,
• Flammable materials
• Oil or grease (especially be careful in use of hand cream)
• Water
• Dust
The product and its associated equipment must be prevented from fall-
ing over.
Always maintain oxygen cleanliness standards,
Use only the product and its associated equipment in a well ventilated
area.
O2
AIR
N2O
e.g. O2+N2O
VAC
3/191
EN

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