Packaging for terminally sterilized medical devices - Sealable pouches and reels of porous materials and plastic film construction. Requirements and test methods Ingestion-build-239834 • The implementation of CEN

• The implementation of CEN amendment A1:2008

BS EN 16842‑7 deals with all significant hazards

2 Special verification

this standard provides useful information that may be more difficult to find elsewhere especially when dealing with measurements that refer to old units

within or outside a court of law

Packaging for terminally sterilized medical devices - Sealable pouches and reels of porous materials and plastic film construction. Requirements and test methods Ingestion-build-239834 • The implementation of CENWhat 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.