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16. Any person who connects external
equipment to signal input and signal output
ports or other connectors has formed a
system and is therefore responsible for the
system to comply with the requirements of
IEC 60601-1. If in doubt, contact a qualified
Biomedical technician or your local
representative.
17. This equipment has been tested and found
to comply with the Class A limits for medical
devices to the 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 and, if not installed and
used in accordance with the instructions,
may cause harmful interference to other
device(s) 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:
(a) Reorient or relocate the receiving
device.
(b) Increase the separation between the
equipment.
(c) Connect the equipment into an outlet on
a circuit different from that to which the
other devices are connected.
(d) Consult the manufacturer or field service
technician for help.
This unit was not evaluated for use with
electrosurgical devices which access the
site via the same endoscope as the light
source and camera. The unit must be re-
evaluated prior to use with electrosurgical
devices when they will operate through the
same endoscope as the light source and
camera.
18. After each use, thoroughly clean unit and
accessories (See “Cleaning and
Sterilizing”).
NOTES:
1. Observe all national waste management
regulations.
2. Do not dispose of WEEE as unsorted
municipal waste.
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