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ISO 18113-1:2009

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

Standard Details

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Status : WITHDRAWN
Standard Type: Main
Document No: ISO 18113-1:2009
Document Year: 2009
Pages: 49
Edition: 1
  • Section Volume:
  • 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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WITHDRAWN
ISO 18113-1:2009
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