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DS/EN ISO 18113-1:2024

Current

Current

The latest, up-to-date edition.

In vitro diagnostic medical devices– Information supplied by the manufacturer (labelling)– Part1:Terms, definitions, and general requirements (ISO 18113-1:2022)

Published date

19-06-2024

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This document defines concepts, establishes general principles, and specifies essential requirements for information supplied by the manufacturer of IVD medical devices.

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

Standards Relationship
EN ISO 18113-1:2024 Identical
ISO 18113-1:2022 Identical

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