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Cross References:
EN 980
ISO 8601
ISO 14971
ISO 15198
ISO 15223
ISO 18113-1
ISO 17511:2003
ISO 18113-3
ISO 18153:2003
ISO/IEC Directives
EN 375:2001
CLSI C28-A2:2000
CLSI GP10-A:1995
98/79/EC:1998
 

Document History

  1. BS EN ISO 18113-2:2024


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

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


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

    • Historical Version
  3. BS EN ISO 18113-2:2009


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

    • Historical Version
  4. BS 06/30146515 DC

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    BS ISO 18113-2. Clinical laboratory testing and in vitro diagnostic medical systems. Information supplied by the manufacturer (labelling). Part 2. In vitro diagnostic reagents for professional use

    • Historical Version
  5. BS EN 375:2001


    Information supplied by the manufacturer with in vitro diagnostic reagents for professional use

    • Historical Version
  6. BS EN 375:1992


    Specification for labelling of in vitro diagnostic reagents for professional use

    • Historical Version