6 Reprocessing instructions | Perseus A500
Reprocessing
3.2 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 (e.g., concerning the reprocessing cycles).
3.3 Classifications for reprocessing
3.3.1 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 of infection
Sample lines are contaminated as a result of the breathing gas passing
through.
Replace the sample lines in accordance with the corresponding instructions
for use.
CAUTION
Risk of injury to patients due to failure of accessories
Disposable products, such as the sample line and water trap were designed,
tested, and manufactured for single use only. Reuse, reprocessing, or sterilization
can lead to the failure of accessories, incorrect measurements and injuries to the
patient.
– Do not reuse disposable products.
– Do not reprocess disposable products.
– Do not use any disinfectants.
– Do not reprocess with elevated pressure from syringes or compressed air.
Classification Explanation
Non-critical Components that come only into contact with skin that is
intact
Semi-critical Components that carry breathing gas or come into contact
with mucous membranes or pathologically altered skin
Critical Components that penetrate skin or mucous membranes or
come into contact with blood
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