Terumo CDI 550, Operator'S Manual

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system specifications appendix b B-7
Classifications: This equipment is Type CF and Class 1. Classified
by Underwriters Laboratories with respect to electric
shock, fire and mechanical hazards only in accor-
dance with UL 60601-1 <5P30>
In accordance with UL 60601-1: This equipment has
been tested and found to comply with the limits for
medical devices to the IEC 60601-1-2:2014. 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 follow-
ing 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 of the receiving device for
help.