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ISO 18113-3:2009
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In vitro diagnostic medical devices -- Information supplied by the manufacturer (labelling) -- Part 3: In vitro diagnostic instruments for professional use

Abstract

ISO 18113-3:2009 specifies requirements for information supplied by the manufacturer of in vitro dignostic (IVD) instruments for professional use.

ISO 18113-3:2009 also applies to apparatus and equipment intended to be used with IVD instruments for professional use.

ISO 18113-3:2009 can also be applied to accessories, where appropriate.

 

  • Document published on: 2009-12-15
    Edition: 1 (Monolingual) ICS: 11.100.10
    Status: Published Stage: 90.60 (2015-03-18)
    TC/SC: ISO/TC 212 Number of Pages: 9
  • No revision information available

  • No corrigenda or amendments available

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