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DS/EN ISO 18113-2:2024

Current

Current

The latest, up-to-date edition.

In vitro diagnostic medical devices– Information supplied by the manufacturer (labelling)– Part2:In vitro diagnostic reagents for professional use (ISO 18113-2:2022)

Published date

19-06-2024

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

Committee
DS/S-260
DocumentType
Standard
PublisherName
Danish Standards
Status
Current
Supersedes

Standards Relationship
ISO 18113-2:2022 Identical
EN ISO 18113-2:2024 Identical

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