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ÖNORM EN ISO 17664-2:2024 08 01
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Reprocessing of healthcare products - Information to be provided by the medical device manufacturer for the reprocessing of medical devices - Part 2: Non-critical medical devices (ISO 17664-2:2021)
Hardcopy
German - English
01-08-2024
This document specifies requirements for the information to be provided by the medical device manufacturer for the reprocessing of non-critical medical devices for which sterilisation is not provided (i.e. medical devices intended only for contact with intact skin or not for direct patient contact).
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