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BS EN 868-2:2017

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

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Packaging for terminally sterilized medical devices Sterilization wrap. Requirements and test methods

Available format(s)

Hardcopy , PDF

Language(s)

English

Published date

28-02-2017

Superseded date

07-05-2025

Superseded by

BS EN 868-2:2025

€263.42
Excluding VAT
Summarise this standard

European foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Requirements
5 Information to be supplied by the manufacturer
Annex A (informative) - Details of significant technical
        changes between this European Standard and the
        previous edition
Annex B (informative) - Method for the determination
        of drape
Annex C (normative) - Method for the determination
        of water repellency
Annex D (normative) - Method for the determination
        of pore size
Annex E (informative) - Repeatability and reproducibility
        of test methods
Bibliography

Defines test methods and values for materials for sterile barrier systems and/or packaging systems that are intended to maintain sterility of terminally sterilized medical devices to the point of use.

Committee
CH/198
DevelopmentNote
Supersedes BS 6254(1989) (10/1999) Supersedes 92/58622 DC (08/2005) Supersedes BS 6255(1989) (09/2005) Supersedes 07/30166924 DC. (10/2009) Supersedes 15/30325855 DC. (02/2017)
DocumentType
Standard
Pages
28
PublisherName
British Standards Institution
Status
Superseded
SupersededBy
Supersedes

This draft European Standard provides test methods and values for materials for sterile barrier systems and/or packaging systems that are intended to maintain sterility of terminally sterilized medical devices to the point of use. The need for a protective packaging may be determined by the manufacturer and the user. This part of EN 868 only introduces performance requirements and test methods that are specific to the products covered by this part of EN 868 but does not add or modify the general requirements specified in EN ISO 11607-1. As such, the particular requirements in 4.2 can be used to demonstrate compliance with one or more but not all of the requirements of EN ISO 11607-1. When additional materials are used inside the sterile barrier system in order to ease the organization, drying or aseptic presentation (e.g. inner wrap, container filter, indicators, packing lists, mats, instrument organizer sets, tray liners or an additional envelope around the medical device) then other requirements, including the determination of the acceptability of these materials during validation activities, may apply. The materials specified in 4.2.2.1 to 4.2.2.3 of this part of EN 868 are intended for single use, the materials specified in 4.2.2.4 are intended for reuse.

Standards Relationship
NEN EN 868-2 : 2017 Identical
NS EN 868-2 : 2017 Identical
I.S. EN 868-2:2017 Identical
NBN EN 868-2 : 2009 Identical
NF EN 868-2 : 2017 Identical
EN 868-2:2017 Identical
DIN EN 868-2:2015-08 (Draft) Identical
DIN EN 868-2:2017-05 Equivalent
UNE-EN 868-2:2017 Identical
DIN EN 868-2:2017-05 Identical

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A newer version of this standard is available.

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€263.42
Excluding VAT