Sunoptic Surgical; Contraindications - Sunoptic Surgical SSLW-0100 Manuel D'utilisation

PLEASE READ BEFORE USE
Failure to follow these instructions could render the device unusable and void any
warranty.
DEVICE DESCRIPTION/DEVICE CLASSIFICATION
SSLW-0100 Light Wand – Class II US FDA, Class lla EU

SUNOPTIC SURGICAL

when coupled to
SURGICAL fiberoptic light guides can be used with quartz halogen, metal halide, or
®
xenon light sources.
INTENDED USE
This device is designed to illuminate a surgical site by relaying light from a fiberoptic light
source on to the desired site. SUNOPTIC SURGICAL
high transmittance, peak efficiency.

CONTRAINDICATIONS

This device has no contraindications that of which we have knowledge.
WARNINGS & PRECAUTIONS
The user of this product should be thoroughly familiar and trained in use and
care of the product. Use caution to treat SUNOPTIC SURGICAL
would any fine optical device.
SUNOPTIC SURGICAL
sterilized before use. See instructions for cleaning and sterilization
Always inspect the light guide for any evidence of damage prior to use. Pay
particular attention to optical surfaces looking for scratches or dings
Use caution to treat SUNOPTIC SURGICAL
optical device
For use with 300 watt xenon light source be sure light source is filtering at least
90% of Infrared Radiation to prevent high heat
The user of this product should be thoroughly familiar and trained in use and
care of the product
LIT154 SUNOPTICS SURGICAL
(English)
®
fiberoptic light guides are designed to deliver maximum light
a medical grade
®
light guides are provided non-sterile and must be
®
fiberoptic light source.
® light guides are medical grade,
® light guides as you
® light guides as you would any fine
SUNOPTICS
Rev. B
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