International Standard
ISO 18113-2:2022
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2: In vitro diagnostic reagents for professional use
Reference number
ISO 18113-2:2022
Edition 2
2022-10
© ISO 2024
International Standard
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Published (Edition 2, 2022)

ISO 18113-2:2022

Format
Language
CHF 63
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Abstract

This document specifies requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) reagents, calibrators and controls intended for professional use.

This document can also be applicable to accessories.

This document is applicable to the labels for outer and immediate containers and to the instructions for use.

This document does not apply to:

a) IVD instruments or equipment;

b) IVD reagents for self-testing.

General information

  • Status
     : Published
    Publication date
     : 2022-10
    Stage
    : International Standard published [60.60]
  • Edition
     : 2
    Number of pages
     : 11
  • Technical Committee :
    ISO/TC 212
    ICS :
    11.100.10 
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