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BS EN ISO 6717:2021 - TC

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Tracked Changes. In vitro diagnostic medical devices. Single-use containers for the collection of specimens from humans other than blood

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  • AS/NZS 4308:2023

    Procedures for specimen collection and the detection and quantification of drugs in urine

  • BS EN 13532:2002

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

  • 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 ISO 6717:2021 - TC

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$418.26 NZD

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