PROTEUS XR/a
GE MEDICAL SYSTEMS
Operator Manual
REV 11
DIRECTION 2259724-100
v
ELECTROMAGNETIC COMPATIBILITY (EMC)
This product conforms with IEC 60601-1-2:2001 EMC standard for medical devices.
Note
:
This equipment generates, uses, and can radiate radio frequency energy. The
equipment may cause or subject to radio frequency interference with other
medical and non–medical devices and radio communications. To provide
reasonable protection against such interference, the Proteus XR/a System (32,
50, 65, 80kW) complies with emissions limits for a Group 1, Class A Medical
Devices and has applicable immunity level as stated in EN 60601-1-2:2001.
However, there is no guarantee that interference will not occur in a particular
installation. Special precautions and other information regarding EMC provided
in the accompanying documents of this equipment shall be observed during
installation and operation of this equipment.
Note
:
If this equipment is found to cause interference (which may be determined by
switching the equipment on and off), the user (or qualified service personnel)
should attempt to correct the problem by one or more of the following
measure(s):
•
Reorient or relocate the affected device(s).
•
Increase the separating space between the equipment and the affected
device.
•
Power the equipment from a source different from that of the affected
device.
•
Consult the point of purchase or service representative for further
suggestions.
Use of accessories, transducers, cables and other parts other than those
specified by the manufacturer of this equipment may result in increased
emissions or decreased immunity of the equipment. The manufacturer is not
responsible for any interference caused either by the use of interconnect
cables other than those recommended, or by unauthorized changes or
modifications to this equipment. Unauthorized changes or modifications could
void the user’s authority to operate the equipment.
WARNING
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