DS/EN ISO 11607-2:2020/A1:2023
Current
Current
The latest, up-to-date edition.
Packaging for terminally sterilized medical devices – Part 2: Validation requirements for forming, sealing and assembly processes – Amendment 1: Application of risk management
Amendment of
Published date
01-11-2023
Publisher
Sorry this product is not available in your region.
This document specifies requirements for the development and validation of processes for packaging medical devices that are terminally sterilized.
Committee |
DS/S-259
|
DocumentType |
Amendment
|
PublisherName |
Danish Standards
|
Status |
Current
|
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.