Packaging for terminally sterilized medical devices - Sealable pouches and reels of porous and plastic film construction. Requirements and test methods Ingestion-build-86103 The principles of this standard

The principles of this standard can be applied to other fusion welding processes subject to agreement between the contracting parties

Screening of cabling elements

This standard does not deal with the tactility or visibility of flags or with permeable flags

vulnerabilities and risk assessment methods

This European Standard does not cover discharge indicating pressure switches

Packaging for terminally sterilized medical devices - Sealable pouches and reels of porous and plastic film construction. Requirements and test methods Ingestion-build-86103 The principles of this standardBS EN 868 5: 2009 Packaging for terminally sterilized medical devices. Sealable pouches and reels of porous and plastic film construction. Requirements and test methods Part 1 of the BS EN 868 series of European standards specifies general requirements and test methods for all packaging materials and systems intended for use as packaging for medical devices which are to be terminally sterilized in their packaging. BS EN 868 5 provides examples of