Eighteeth E-FLOW User Manual page 33

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Storage: Store the sterilized components in a dry, clean and dust free
environment at modest temperatures, refer to labels and instructions
for use.
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The instructions provided above have been validated by the manufacturer of
the medical device as being capable of preparing a medical device for use. It
remains the responsibility of the processor to ensure that the processing, as
actually performed using equipment, materials and personnel in the processing
facility, achieves the desired result. This requires verification and/or validation
and routine monitoring of the process. Likewise, any deviation by the processor
from the instructions provided should be properly evaluated for effectiveness
and potential adverse consequences.
digital records of cycles parameters).
The sterilization procedure must comply with EN ISO 17665.
Waiting for cooling before touching.
Sterility cannot be guaranteed if packaging is open, damaged or
wet.
Check the packaging before using it (packaging integrity, no
humidity and validity period).
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