ISO 18113-1:2009
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements
Reference number
ISO 18113-1:2009
Edition 1
2009-12
© ISO 2024
Withdrawn
Withdrawn (Edition 1, 2009)

Abstract

ISO 18113-1:2009 defines concepts, establishes general principles and specifies essential requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) medical devices.

General information

  • Status
     : Withdrawn
    Publication date
     : 2009-12
    Stage
    : Withdrawal of International Standard [95.99]
  • Edition
     : 1
    Number of pages
     : 49
  • Technical Committee :
    ISO/TC 212
    ICS :
    11.100.10 
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