10. Use only manufacturer's specified compatible accessories and peripheral equipment. Use of
non-approved equipment may cause loss of function.
11. Before each use, check the outer surface of this equipment to be used to ensure that there
are no rough surfaces, sharp edges, or protrusions that can cause injury.
12. Avoid dropping the camera system or rough handling. The camera system contains sensitive
components prone to damage by mechanical shock.
13. This device complies with the IEC 60601-1 safety standard. When peripherals are connected
to this device, a Medical Electrical (ME) System is formed and the system should be evaluated
for conformance to IEC 60601-1 safety standards. When used with other equipment, the
leakage currents may be additive. The person creating the ME system is responsible to
comply with the applicable safety regulations and safety standards for their location. Connect
only IEC 60601-1 approved equipment to this device. Never touch peripheral equipment
connections on this device and the patient at the same time. This can create a risk of shock
to the patient.
14. Do not use the equipment in the prescence of flammable liquids, gases, or other materials
susceptible to ignition due to electrical sparking.
15. This equipment generates and radiates RF energy which may affect the normal function of
nearby installed equipment. Equipment that generates and radiates RF energy may affect
the normal function of the HD Camera System. When choosing a location for the HD Camera
System, consult the "Electromagnetic Compatibility" section of this manual to ensure proper
function with other installed equipment.
Cautions
To prevent improper use and/or damage to this device, please note the following cautions:
1. Carefully unpack this unit and check if any damage occurred during shipment. If damage is
detected, refer to the Warranty and Return Policy section of this manual.
2. This equipment generates heat and uses cooling fans during normal use. To reduce the risk
of overheating and possible loss of function and/or damage to the equipment, install the
equipment in a well-ventilated space within the operating conditions listed herein.
3. There is a risk of damage to the equipment if the equipment is subjected to cleaning or
sterilization methods not approved be the manufacturer. To reduce risk of loss of funtion
and/or damage to the equipment, only use the approved cleaning and sterilization methods
described herein.
4. High frequency surgical devices may cause interference with the video image displayed on
the surgical monitor. To reduce this risk, high frequency devices and imaging equipment
should be located on separate supply circuits.
5. There are no user serviceable parts inside the console or camera heads. There are hazardous
voltages present inside the console. Do not remove the cover. Return the device to the
manufacturer for service.
NOTE:
The warranty is void if any of these warnings or cautions are disregarded
LIT-239 SUNOPTIC SURGICAL
Rev. B
®
Page 6 of 210
(English)