Allied Healthcare ResusciTIMER 매뉴얼 - 페이지 6
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페이지 인쇄§
Internally powered device.
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IP20 degree of protection against ingress of water.
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Equipment not suitable for use in presence of a flammable anesthetic mixture with air or with oxygen or
nitrous oxide.
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Suitable for continuous operation.
This equipment has been tested and found to comply with the EMC limits for the Medical Device Directive 93/42/ECN
(EN 55011 and EN 60601-1-2). These limits are designed to provide reasonable protection against harmful interference
in a typical medical installation. The equipment generates, uses and can radiate radio frequency energy and, if not
installed and used in accordance with these 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 with other devices, which can be determined by turning the equipment off and on, the user is
encouraged to try to correct the interference by one or more of the following measures:
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Reorient or relocate the receiving device
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Increase the separation between the equipment
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Connect the equipment into an outlet on a circuit different from that to which the other device(s) is
connected.
Consult the manufacturer or field service technician for help
Degree of protection against electric shock: Type BF
Caution, Consult accompanying documents
% Relative Humidity: 0 to 90%
Temperature Range: -20°F to 140°F
On/Off
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