SR EN 868-6:2025
Packaging for terminally sterilized medical devices - Part 6: Paper for low temperature sterilization processes - Requirements and test methods
This document specifies test methods and values for paper used in the manufacture of single-use preformed sterile barrier systems and/or packaging systems for terminally sterilized medical devices by means of low temperature sterilization processes. Other than the general requirements as specified in EN ISO 11607-1 and EN ISO 11607-2 [2], this part of EN 868 specifies materials, test methods and values that are specific to the products covered by this document.
Status :
Valid
Approval date : 5/30/2025
Number of pages : 24
ICS : 11.080.30 Steriliyed packaging
Technical Committee : 377 - Medical devices
- Replaces SR EN 868-6:2017
RO