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ENGLISH
INSTRUCTION FOR USE: MEDICONNECT DUOLINE
1. FOREWORD
MEDICONNECT-DUOLINE are medical devices classifi ed as class IIa medi-
cal devices according to the Medical Device Directive 93/42/EEC. Their
compliance with the requirements of the 93/42/EEC Medical Device Direc-
tive is based upon the EN ISO 5359 standard.
2. INTENDED USE
MEDICONNECT-DUOLINE are intended for the transfer of medical gases
or vacuum, and/or the connection of two medical products (e.g. a pressure
regulator with an emergency ventilator).
3. OPERATIONAL, TRANSPORT AND STORAGE
SAFETY REQUIREMENTS
Keep the product and its associated equipment away from:
• All sources of heat
• Flammable materials
• Oil or grease (including all hand creams)
• Water
• Dust.
Always maintain oxygen cleanliness standards.
Use only the product and its associated equipment in a well ventilated
area.
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.
OPERATING CONDITIONS
-10/+40 °C
5/95%
STORAGE AND TRANSPORT
CONDITIONS
-10/+40 °C
5/95%
3/96
EN
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