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CEN - EN 868-10

Packaging for terminally sterilized medical devices - Part 10: Adhesive coated nonwoven materials of polyolefines - Requirements and test methods

inactive
Organization: CEN
Publication Date: 1 May 2009
Status: inactive
Page Count: 16
ICS Code (Sterilized packaging): 11.080.30

Document History

EN 868-10
December 1, 2018
Packaging for terminally sterilized medical devices - Part 10: Adhesive coated nonwoven materials of polyolefines - Requirements and test methods
This document specifies test methods and values for sealable adhesive coated nonwoven materials of polyolefines, manufactured from nonwovens complying with EN 868‑9 used for sterile barrier systems...
EN 868-10
May 1, 2009
Packaging for terminally sterilized medical devices - Part 10: Adhesive coated nonwoven materials of polyolefines - Requirements and test methods
A description is not available for this item.
EN 868-10
February 1, 2000
Packaging Materials and Systems for Medical Devices Which Are to Be Sterilized - Part 10: Adhesive Coated Nonwoven Materials of Polyolefines for Use in the Manufacture of Heat Sealable Pouches, Reels and Lids - Requirements and Test Methods
A description is not available for this item.

References

This document is referenced by:
SN EN ISO 25424/A1 - Sterilization of health care products - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices Amendment A1
Published by SNV on May 1, 2022
A description is not available for this item.
This document is referenced by:
EN ISO 11607-1 - Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems
Published by CEN on January 1, 2020
This document specifies requirements and test methods for materials, preformed sterile barrier systems, sterile barrier systems and packaging systems that are intended to maintain sterility of...
This document is referenced by:
EN ISO 17665-1 - Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices
Published by CEN on August 1, 2006
Inclusions This part of ISO 17665 specifies requirements for the development, validation and routine control of a moist heat sterilization process for medical devices. NOTE Although the scope of this...
This document is referenced by:
ISO TS 17665-3 - Sterilization of health care products — Moist heat — Part 3: Guidance on the designation of a medical device to a product family and processing category for steam sterilization
Published by ISO on April 15, 2013
This part of ISO 17665 provides guidance about the attributes of a medical device to be considered by the user when assigning a medical device to a product family for the purpose of identifying and...
This document is referenced by:
CSA Z17665-1 - Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices
Published by CSA on January 1, 2009
Inclusions This part of ISO 17665 specifies requirements for the development, validation and routine control of a moist heat sterilization process for medical devices. NOTE Although the scope of this...
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