Arthrex AR-3200-1018, Инструкция по эксплуатации

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4. For the protection of the patient it is
essential that the Synergy Laser Light
Source to Synergy
ID
endoscopic video
system interconnection is complete and
the Synergy
ID
endoscopic video system is
able to activate the Synergy Laser Light
Source in fluorescence mode PRIOR to
administration of patient anesthesia.
5. Only the physician can evaluate the
clinical factors involved with each patient
and determine if the use of this device is
indicated. The physician must determine
the specific technique and procedure that
will accomplish the desired clinical effect.
6. This device and its accessories are to be
used only by physicians and medical
assistants under the direction of a
physician with appropriate technical
qualifications.
7. Use of accessories and cables other than
those specified or provided by the
manufacturer of this equipment could
result in increased electromagnetic
emissions or decreased electromagnetic
immunity of this equipment and result in
improper operation. This device shall only
be used with original and manufacturer’s
accessories and replacement parts. Use
of other parts or materials may degrade
device safety.
8. Do not use in the presence of flammable
anesthetics, gases, disinfecting
agents, cleaning solutions, or
any material susceptible to
ignition due to electrical
sparking.
9. Equipment grounding is vital for safe
operation. Plug the power cord into a
properly earthed mains supply outlet
whose voltage and frequency
characteristics are compatible with those
listed on the unit or in this manual. Do not
use plug adapters or extension cords;
such devices defeat the safety ground and
could cause injury.
10. This equipment should not share an
electrical outlet or grounding with life
supporting or life sustaining equipment.
11. If one or more mains powered units are
connected simultaneously to one socket
by the means of a distribution box, the
sum of the individual leakage currents
may exceed the tolerated limits.
12. For the protection of service personnel,
and for safety during transportation, all
devices and accessories that are returned
for repair must be prepared for shipment
as described in “
Returning the Device”
of this manual. The manufacturer has the
right to refuse to carry out repairs if the
product is contaminated.
13. This equipment/system may cause radio
interference or may disrupt the operation
of nearby equipment. It may be necessary
to take mitigation measures, such as re-
orienting or relocating the Synergy Laser
Light Source or shielding the location.
14. NOT for use in an Oxygen Rich
Environment.
15. NO Modifications of this equipment are
allowed.
16. Connecting any equipment that has not
been supplied as part of this ME System
to Multiple Socket Outlets may result in
increased leakage currents. Use an IEC
Approved Isolation Transformer to isolate
any such interconnections from the ME
System.
17. Risk of burns!
Light Engines emit large amounts of light and
thermal energy. (Note: activation of the
Synergy Laser Light Source is controlled by
the Synergy
ID
system.) As a result:
• Always keep the Synergy ID LED Light
Engine in the STANDBY mode when not
in use. This, in turn, will keep the
Synergy Laser Light Source off. The
endoscope light guide connection can
get extremely hot as result of high
intensity light, giving rise to high
temperatures in front of the light
emission window which may cause
severe burns.
• Surface temperatures of the insertion
portion of the endoscope as well as light
guide connectors on the Synergy
ID
Camera Control Unit (CCU), the
Synergy Laser Light Source, and the
endoscope rise during use.