Standard

SN EN ISO 18113-3:2024

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Abstract

This document specifies requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) instruments intended for professional use. This document also applies to apparatus and equipment intended to be used with IVD instruments for professional use. This document can also be applicable to accessories. This document does not apply to: a) instructions for instrument servicing or repair; b) IVD reagents, including calibrators and control materials for use in control of the reagent; c) IVD instruments for self-testing.

Products specifications

  • Standard from INB
  • Published:
  • Effective:
  • Document type: EN
  • Publisher: SNV
  • Distributor: SNV
  • ICS: 11.100.10
  • National Committee: INB/NK 157

Legal references

Swiss Federal Authority: SWISSMEDIC
Designated under following Swiss law: 812.213
Designated under following EU law: Regulation (EU) 2017/746

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