Packaging for terminally sterilized medical devices - 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 Ingestion-build-141043 BS 3955:1986

BS 3955:1986

The method can be used for quality control but has some limitation in relation to ISO 11092

that the nuts constituting the batch satisfy the requirements of BS EN 3899

The biological response to the coating of hydroxyapatite ceramic has been demonstrated by a history of its clinical use and by laboratory studies

It must be taken care that the materials used in buildings

Packaging for terminally sterilized medical devices - 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 Ingestion-build-141043 BS 3955:1986What is BS EN 868 3 Packaging for terminally sterilized medical devices about? BS EN 868 3 is the third part of the EN 868 multi series that discusses packaging for terminally sterilized medical devices. BS EN 868 3 specifies test methods and values for paper, used in the manufacture of paper bags (specified in BS EN 868 4) and in the manufacture of pouches and reels (specified in BS EN 868 5) used as sterile barrier systems and or packaging systems