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TABLE OF CONTENTS

2

Indication for Use  

 

 2 

 

Care and Maintenance 

 

 6 

General Warnings  

 

 

 Troubleshooting 

 

   6 

Assembly  

 

 

 3-4 

 

Luxtec Equipment Warranty   

 7 

Adjustments    

 

 4-5 

 

Luxtec Cable Warranty  

 

 7 

Replacement Part Numbers    5 

 

Repair and Return  

 

 

 7 

INDICATION FOR USE

This fiber optic light guide system is designed 
to deliver illumination from a high intensity 
light source to a surgical headlight for surgical 
site illumination, either standard or minimally 
invasive. While the cable light source 
endfittings are compatible with all light 
sources, brightness and spot quality vary with 
specific types of light sources.  The xenon 

UltraLite systems perform best with Luxtec 
xenon light sources. 
 

Any light source used with this cable should 
have a maximum output of 0.25W IR at the 
cable port to prevent cable and/or headlight 
damage during use.

 

GENERAL WARNINGS

The user of this product should be thoroughly familiar 
and trained in the use and care of this product. 
 
The user should carefully study this manual before 
making any attempt to use the product clinically.  
Instructions should be followed specifically, with 
special attention given to warnings and cleaning 
instructions. This manual should also be available to 
the surgical team during a procedure. 
 
Follow the instructions in the operating manuals of 
other manufacturer’s equipment when they are use in 
conjunction with this product. 
 
Before every procedure, carefully inspect the light 
guide cable to ensure it has been properly maintained, 
cleaned and sterilized (if compatible), and that it is 
fully functional. 
 
Any light source used with this cable should have a 
maximum output of 0.25W IR at the cable port to 
prevent cable and/or headlight damage during use. 
 

Light sources use high intensity lamps, which 
produce heat as well as brilliant light.  The high 
brightness produced by the light source and the light 
output of the light guide cable can cause burns. 
Care should be taken to follow the maintenance and 
cleaning instructions.  Excessive bending of the cable 
should be avoided. 
Use care not to point the light guide directly at the 
eye while in operation.  The brilliant light output can 
cause severe eye discomfort. 
 

FIRE HAZARD: DO NOT DRAPE OR 
COVER THE LIGHT SOURCE OR THE 
LIGHT GUIDE WHILE IT IS OPERATING.  
DO NOT PLACE THE LIGHT GUIDE ON A 
DRAPE WHILE IT IS OPERATING. 
 
CAUTION: The metal portions of the cable at 
the light source get hot during operation.  
Allow components to cool outside of the light 
source for at least 5 minutes before touching.

 

Summary of Contents for UltraLife

Page 1: ...UltraLite Headlight Operation and Service Manual ENGLISH...

Page 2: ...ng instructions This manual should also be available to the surgical team during a procedure Follow the instructions in the operating manuals of other manufacturer s equipment when they are use in con...

Page 3: ...to curve gently around the shape of the headband All illustrations are representative and may not reflect your actual model and accessories HEADBAND properly supported Remove the cable from the module...

Page 4: ...burns Figure 3 SWEATBAND HEADBAND Fiber optic cable Cable Clips Headlight module Joystick Headlight module Joystick Fiber optic cable Cable Clips Figure 4 HEADBAND SWEATBAND Cable Clip Cable Clips Ad...

Page 5: ...ralite 2 bifurcated cable Ultralite module and extended linkage AX 1375 BIF SL Headband with Ultralite 2 bifurcated cable and Ultralite module AX 1385 BIF SL Sweatband with Ultralite 2 bifurcated cabl...

Page 6: ...e the cables in sterilization trays for additional protection Any inadvertent cut or puncture to the silicone tube will render the cable unsafe It should be taken out of service immediately Cleaning M...

Page 7: ...romptly reports such a defect to LUXTEC in writing 2 If requested by LUXTEC customer returns equipment to LUXTEC with shipping charges pre paid and 3 Upon inspection LUXTEC finds the cable to be defec...

Page 8: ...s the Essential Requirements specified in Annex 1 of the Medical Device Directive MDD 99 Hartwell Street West Boylston MA 01583 USA Telephone 1 800 325 8966 US only or 1 508 835 9700 Facsimile 1 508 8...

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