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Cross References:
EN 980
ISO 8601
ISO 14971
ISO 15198
ISO 15223
ISO 18113-1
ISO 17511:2003
ISO 18113-5
ISO 18153
ISO/IEC Directives
EN 376:2001
CLSI C28-A2:2000
CLSI GP10-A.:1995
98/79/EC:1998
GHTF/SG1/N43:2005
 

Document History

  1. BS EN ISO 18113-4:2024


    In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling)-In vitro diagnostic reagents for self-testing

    • Most Recent
  2. BS EN ISO 18113-4:2011


    In vitro diagnostic medical Devices. Information supplied by the manufacturer (labelling)-In vitro diagnostic reagents for self-testing

    • Historical Version
  3. BS EN ISO 18113-4:2009


    In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling)-In vitro diagnostic reagents for self-testing

    • Historical Version
  4. BS 06/30146522 DC

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    BS ISO 18113-4. Clinical laboratory testing and in vitro diagnostic medical systems. Information supplied by the manufacturer (labelling). Part 4. In vitro diagnostic reagents for self-testing

    • Historical Version
  5. BS EN 376:2002


    Information supplied by the manufacturer with in vitro diagnostic reagents for self-testing

    • Historical Version
  6. BS EN 376:1992


    Specification for labelling of in vitro diagnostic reagents for self-testing

    • Historical Version