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BS EN ISO 6717:2021

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

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Related Information

Similar Standards

  • 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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Pages: 22

Previous versions

BS EN ISO 6717:2021

Get this standard Prices exclude GST
PDF ( Single user document)
$306.96 NZD
PDF ( Single user document)
$275.72 NZD
HardCopy
$343.48 NZD

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BS EN ISO 6717:2021

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