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     :  Withdrawn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
  • Edition
     : 1
    Number of pages
     : 49
  • Technical Committee
     : ISO/TC 212 Clinical laboratory testing and in vitro diagnostic test systems
  • ICS
     :
    11.100.10 In vitro diagnostic test systems

Life cycle


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