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Document History

  1. DIN EN ISO 18113-1


    In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)

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  2. DIN EN ISO 18113-1


    In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)

    • Historical Version
  3. DIN EN ISO 18113-1 - DRAFT

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    Draft Document - Clinical laboratory testing and in vitro diagnostic medical systems - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO/DIS 18113-1:2006); German version prEN ISO 18113-1:2006

    • Historical Version