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CEN - EN 868-3

Packaging for terminally sterilized medical devices - Part 3: Paper for use in the manufacture of paper bags (specified in EN 868-4) and in the manufacture of pouches and reels (specified in EN 868-5) - Requirements and test methods

inactive
Organization: CEN
Publication Date: 1 May 2009
Status: inactive
Page Count: 20
ICS Code (Sterilized packaging): 11.080.30

Document History

EN 868-3
February 1, 2017
Packaging for terminally sterilized medical devices - Part 3: Paper for use in the manufacture of paper bags (specified in EN 868-4) and in the manufacture of pouches and reels (specified in EN 868-5) - Requirements and test methods
This European Standard specifies test methods and values for paper, used in the manufacture of paper bags (specified in EN 868-4) and in the manufacture of pouches and reels (specified in EN 868-5)...
EN 868-3
May 1, 2009
Packaging for terminally sterilized medical devices - Part 3: Paper for use in the manufacture of paper bags (specified in EN 868-4) and in the manufacture of pouches and reels (specified in EN 868-5) - Requirements and test methods
A description is not available for this item.
EN 868-3
June 1, 1999
Packaging Materials and Systems for Medical Devices Which Are to Be Sterilized - Part 3: Paper for Use in the Manufacture of Paper Bags (Specified in EN 864-4) and in the Manufacture of Pouches and Reels (Specified in EN 868-5) - 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:
EN IEC 60684-3-247 - Flexible insulating sleeving - Part 3: Specifications for individual types of sleeving - Sheet 247: Heat-shrinkable, polyolefin sleeving, dual wall, not flame retarded, thick and medium wall
Published by CENELEC on October 1, 2019
This part of IEC 60684 gives the requirements for two types of heat-shrinkable, polyolefin sleeving, dual wall, not flame retarded with a nominal shrink ratio of 3:1. This sleeving has been found...
This document is referenced by:
EN ISO 14534 - Ophthalmic optics - Contact lenses and contact lens care products - Fundamental requirements
Published by CEN on January 1, 2015
This International Standard specifies safety and performance requirements for contact lenses, contact lens care products, and other accessories for contact lenses. This International Standard does...
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