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Chapter 13. UL /EN Statement
This equipment has been tested and found to comply with the limits for medical devices in IEC/EN
60601-1-2
and FCC/CE. 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 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 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.
-
Type of protection against electric shock: Class I equipment
- Degree of protection against electric shock: Not classified - no applied parts
- Classification according to the degree of protection against ingress of water as detailed in the current
edition of IEC 529: IPX0, ordinary equipment
- This equipment is not suitable for use in the presence of flammable anesthetics or oxygen
- Mode of operation: continuous operation