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Project

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; German and English version FprEN 868-3:2024

Abstract

The EN 868 series of standards have been developed mainly for materials and sterile barrier systems used in health care facilities sterilization processes. The EN 868 series of standards can be used to demonstrate compliance with one or more of the requirements specified in EN ISO 11607-1. Considering CEN guide 4 and the CEN environmental checklists, this revision has been complemented with a new annex with guidance to encourage users to also include environmental aspects when applying the EN 868 series of standards with the objective to minimize the environmental impact. Environmental aspects have also been included into the description of test methods with the same objective. This document has been prepared by Working Committee NA176-03-07AA "Sterile supply" of DIN Standards Committee Health Technologies.

Begin

2023-03-03

WI

00102178

Planned document number

DIN EN 868-3

Project number

06302212

Responsible national committee

NA 176-03-07 AA - Sterile supply  

Responsible european committee

CEN/TC 102/WG 4 - Packaging  

draft standard

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; German and English version prEN 868-3:2024
2024-05
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previous edition(s)

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; German version EN 868-3:2017
2017-05

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Contact

M.Sc.

Maximilian Rasser

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Fax: +49 30 2601-42572

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