Dräger VarioLux User Manual

Instructions for use VarioLux 17
English
Reprocessing
Safety instructions
Information on reprocessing
Follow the national infection prevention policies and reprocessing
regulations.
Follow the infection prevention policies and reprocessing
regulations of the health-care facility.
Classifications for reprocessing
Classification of medical devices
The classification depends on the intended use of the medical
device. The risk of infection transmission through the application
of the product to the patient without proper reprocessing is the
basis of the Spaulding classification.
WARNING
Risk due to inappropriately reprocessed products
Products must be reprocessed, otherwise there is an in-
creased risk of infection.
– Follow the infection prevention policies and reprocess-
ing regulations of the health-care facility.
– Follow the national infection prevention policies and re-
processing regulations.
– Use validated procedures for reprocessing.
Follow the manufacturer's instructions for cleaning agents
and disinfectants.
CAUTION
Risk due to faulty products
Signs of wear, e.g., cracks, deformation, discoloration, or peel-
ing, may occur with reprocessed products.
Check the products for signs of wear and replace them if neces-
sary.
CAUTION
Risk of burns
Before reprocessing, switch the light off and let it cool down to
room temperature.
Classification Explanation
Non-critical Components that come into contact only
with skin that is intact
Semi-critical Components that carry breathing gas or
come into contact with mucous mem-
branes or pathologically altered skin
Critical Components that penetrate skin or mu-
cous membranes or come into contact
with blood

Dräger VarioLux Specifications

General

Brand	Dräger
Model	VarioLux
Category	Medical Equipment
Language	English