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BS EN 928:1996

Withdrawn Date published:

Warning: Withdrawn Standard. This document has been withdrawn without replacement. You may wish to search for a more up to date equivalent.

Guidance on the application of EN 29001 and EN 46001 and of EN 29002 and EN 46002 for in vitro diagnostic medical devices

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Related Information

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  • BS EN 13532:2002

    General requirements for in vitro diagnostic medical devices for self-testing

  • BS EN 13612:2002

    Performance evaluation of in vitro diagnostic medical devices

  • BS EN 13641:2002

    Elimination or reduction of risk of infection related to in vitro diagnostic reagents

  • BS EN 13975:2003

    Sampling procedures used for acceptance testing of in vitro diagnostic medical devices. Statistical aspects

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BS EN 928:1996

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