ÖNORM EN ISO 17664-2:2024 08 01
Current
The latest, up-to-date edition.
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).
Important note : Users cannot be edited or removed once added to your Multi user PDF.Access your standards online with a subscription
Features
-
Simple online access to standards, technical information and regulations.
-
Critical updates of standards and customisable alerts and notifications.
-
Multi-user online standards collection: secure, flexible and cost effective.