Dräger Oxylog VE300 Instrucciones De Uso página 18

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Reprocessing
7 Reprocessing
7.1 Safety information
Risk due to inappropriately reprocessed products
Reusable products must be reprocessed, otherwise there is an increased risk of infection.
► Follow the infection prevention policies and reprocessing regulations of the health-care
► Follow the national infection prevention policies and reprocessing regulations.
► Use validated procedures for reprocessing.
► Reprocess reusable products after every use.
► Follow the manufacturer's instructions for cleaning agents, disinfectants, and
Risk due to faulty products
Signs of wear, e.g., cracks, deformation, discoloration, or peeling, may occur with
reprocessed products.
► Check the products for signs of wear and replace them if necessary.
7.2 Reprocessing procedures
The device holder is categorized as a non-critical product.
The following reprocessing procedures are permitted:
–
–
For information on the disinfection procedure and the approved disinfectants, refer to the
Oxylog VE300 instructions for use.
8 Disposal
8.1 Disposal of the product
At the end of its useful life, dispose of the product in accordance with the applicable legal
provisions.
9 Technical data
9.1 Safety information
Risk of patient injury and damage to the device
The device may not function properly or may fail outside the specified ambient and supply
conditions.
► Only use the device under the specified ambient and supply conditions.
18
WARNING
facility.
reprocessing devices.
CAUTION
Manual cleaning
Disinfection by wiping
WARNING
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Instructions for use Device holder for Oxylog VE300