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SAFETY INFORMATION
Safety Standard
Medical Device Classification
Classification by protection type against Electric
Shock
Classification according to the degree of protection
against ingress of water or particulate matter
Mode of operation
Environment of Use
Applied Part
Regulations
Safety and Electromagnetic Compatibility Information
This equipment has been tested and found to comply with the limits for medical devices in IEC 60601-1-2. 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. If not installed and used in accordance with the
instructions, it 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 turning 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 equipment.
•
Increase the separation between the equipment.
•
Connect the equipment into an outlet on a circuit different from that to which the other devices are connected.
•
Contact manufacturer or authorized agent for help.
Class I equipment and Internally Powered Equipment
IP41
Continuous Operation
This equipment is not suitable for use in the presence of
flammable anesthetic or oxygen.
Type : BF Type, Location : Front of Detector (only for
effective area)
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