Classifications
In accordance with IEC 60601-1
−
Class I and internally powered equipment - the type of protection against electric shock.
−
Type BF or CF equipment. The degree of protection against electric shock is indicated by a
symbol on each parameter module.
−
Equipment is not suitable for use in the presence of a flammable anesthetic mixture with
air or with oxygen or nitrous oxide.
−
Continuous operation according to the mode of operation.
−
Portable Monitor
In accordance with IEC 60529
−
IP21 - degree of protection against harmful ingress of water.
In accordance with EU Medical Device Directive
−
IIb.
In accordance with CISPR 11:
−
Group 1 Class A;
•
Group 1 contains all ISM (Industrial, scientific and medical) equipment in which there
is intentionally generated and/or used conductively coupled radio-frequency energy
which is necessary for the internal functioning of the equipment itself.
•
Class A equipment is equipment suitable for use in all establishments other than
domestic and those directly connected to a low-voltage power supply network
which supplies buildings used for domestic purposes.
Trademarks
Listed below are GE Medical Systems
Information Technologies
and GE Healthcare Finland Oy
trademarks used in this document. All other product and company names contained herein
are the property of their respective owners.
Datex, Ohmeda, DINAMAP, Trim Knob, Unity Network, CARESCAPE, EK-Pro, TruSignal, Entropy,
GE Healthcare, GE Medical system, General Electric Company.
Содержание B20
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Страница 27: ...2 System description ...
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