Packaging for terminally sterilized medical devices - Sealable pouches and reels of porous materials and plastic film construction. Requirements and test methods Ingestion-build-239834 This document describes how to

This document describes how to minimize the effects of differences in temperature

• The implementation of CEN amendment A1:2008

within or outside a court of law

Contents of BS EN ISO 10993-5 include:

BS EN IEC 60512-23-3:2019  includes some technical changes with respect to the previous edition as:

Packaging for terminally sterilized medical devices - Sealable pouches and reels of porous materials and plastic film construction. Requirements and test methods Ingestion-build-239834 This document describes how toWhat is this standard about? This document specifies test methods and values for sealable pouches and reels manufactured from porous materials complying with either EN 868 part 2, 3, 6, 7, 9 or 10 and plastic film complying with Clause 4 of this document. These sealable pouches and reels are used as sterile barrier systems and or packaging systems that are intended to maintain sterility of terminally sterilized medical devices to the point of use.