Equipment Connection - Cuda surgical LLS-2000 Gebrauchsanleitung

2. WARNINGS/CAUTIONS
Caution
practitioner.
Caution
to rain or moisture. Refer all servicing to qualified personnel only.
Caution
oxygen or nitrous oxide.
Caution
cellular phone near the light source.
Caution
have been certified according to IEC 60601-1 for medical equipment and IEC 60601-2-18 for
endoscopic equipment.
Caution
statements of suitability for any purpose.
Caution
equipment. Additional information processing equipment connected to the LED Light Source, a
Medical System and the operator must determine that all equipment complies with the appropriate
end-product standards (such as IEC 60950 or IEC 60065 and the Standard for Medical System, IEC
60601-1-1).
Caution
cable into the unit before turning on the power. When light is not required at the surgical site, the
intensity control should be should be set to the fully dimmed position. If it becomes necessary to
remove the fiber optic cable without turning the unit off, turn the intensity control to the fully dimmed
position.

EQUIPMENT CONNECTION

Caution
CONDUCTIVE CABLE. It should not have conductive shielding or any other conductive connection
between the patient and equipment. Such connection will impair safety of the equipment. It must be
rinsed free of soaking/disinfectant solution and dried before plugging into the LED light source
receptacle. Ensure the optical surface is clean before engaging into the light source.
Caution
unacceptable risk. If this determination is made arrangements should be taken to reduce the risk.
LIT168NR CUDA
(English)
Federal law restricts this device to sale by or on the order of a licensed
To prevent fire or electric shock, do not open or expose the LED light source unit
Not suitable for use in presence of flammable anesthetic mixture with air or with
To prevent any potential electro-magnetic interference, do not use any kind of
This product should be used only with type BF endoscopic instruments which
This symbol indicates type BF equipment.
User must not alter this device in any fashion. Doing so voids all warranties and
All devices connecting to the LED Light Source must be classified as medical
Always set the intensity control to the minimum level and insert the fiberoptic
User is responsible for determining if interruption of light output will create an
®
SURGICAL
-
The fiber optic cable must be
Date of Revision:08/08/14
a NON-
Rev. C
Page 4 of 65