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Cross References:
EN 980
IEC 61010-1
IEC 61010-2-101
IEC 61326
IEC 62366
ISO 14971
ISO 15198
ISO 15223
ISO 18113-1
ISO 18113-2
ISO/IEC Directives
EN 591:2001
98/79/EC:1998
GHTF/SG1/N43:2005
 

Document History

  1. BS EN ISO 18113-3:2024


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

    • Most Recent
  2. BS EN ISO 18113-3:2011


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

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


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

    • Historical Version
  4. BS 06/30146518 DC

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    BS ISO 18113-3. Clinical laboratory testing and in vitro diagnostic medical systems. Information supplied by the manufacturer (labelling). Part 3. In vitro diagnostic instruments for professional use

    • Historical Version
  5. BS EN 591:2001


    Instructions for use for in vitro diagnostic instruments for professional use

    • Historical Version
  6. BS EN 591:1995


    Specification for user manuals for in vitro diagnostic instruments for professional use

    • Historical Version