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2. WARNINGS

To prevent fire or electric shock, do not open or expose the light source unit to rain or
moisture. Refer all servicing to qualified personnel only.
Not suitable for use in presence of flammable anesthetic mixture with air or with oxygen
or nitrate oxide.
This product should be used only with type BF endoscopic instruments which have
been certified according to IEC 601-1 for medical equipment and IEC 601-2-18 for
endoscopic equipment.
This symbol indicates type BF equipment
Caution
!
This product is not provided as sterile.
All devices connecting to the Illuminator must be classified as medical equipment.
Additional information processing equipment connected to the Illuminator, 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
!
Light source can cause permanent eye damage if viewed directly with unprotected eye.
To reduce the chance of eye damage, ser the intensity control always to the minimum
level and insert the fiberoptic cable into the unit before turning on the power.
!
Caution EQUIPMENT CONNECTION
The fiberoptic cable must be
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 light source
receptacle. Ensure the optical surface is clean before engaging into the light source.
®
LIT091 CUDA
SURGICAL
(English)
!
a NON-CONDUCTIVE CABLE.
It should not have
Rev. G
Page 4 of 60

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