FujiFilm Drypix 5000, Operation Manual

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1-5
006-240-20 2004.03
Introduction
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1.5 Electromagnetic Compatibility (EMC)
This equipment has been tested and found to comply with the limits for medical devices to
the EN60601-1-2:1993, Medical Device Directive 93/42/EEC.
These limits are designed to provide reasonable protection against harmful interference in a
typical medical installation.
This equipment generates, uses and can radiate radio frequency energy and, if not installed
and used in accordance with the instructions, may cause harmful interference to other
devices in the vicinity.
However, there is no guarantee that interference will not occur in a particular installation.
If this equipment does cause harmful interference to other devices, which can be
determined by tuning the equipment off and on, the user is encouraged to try to correct the
interference by one or more of the following measures:
• Reorient or relocate the receiving device.
• Increase the separation between the equipment.
• Connect the equipment into an outlet on a circuit different from that to which the other
device(s) are connected.
Consult the manufacturer or field service technician for help.
1.5.1 Classification
1) According to the type of protection against electrical shock
CLASS 1 EQUIPMENT
2) According to the degree of protection against electric shock
NO APPLIED PART
3) Protection against harmful ingress of water
IPXO
4) According to the degree of safety of application in the presence of a flammable anesthetics
mixture with air or with oxygen or nitrous oxide.
Equipment not suitable for use in the presence of a flammable anesthetics mixture with air
or with oxygen or nitrous oxide.
5) According to the mode of operation
CONTINUOUS OPERATION