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SS-EN ISO 18113-1 : 2011

Current

Current

The latest, up-to-date edition.

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)

Available format(s)

Hardcopy

Language(s)

English

Published date

21-11-2011

This part of ISO 18113 defines concepts, establishes general principles and specifies essential requirements for information supplied by the manufacturer of IVD medical devices.

Committee
TC 212
DocumentType
Standard
Pages
0
ProductNote
THIS STANDARD IS IDENTICAL WITH : EN ISO 18113-1 : 2011
PublisherName
Standardiserings-Kommissionen I Sverige
Status
Current

Standards Relationship
ISO 18113-1:2009 Identical

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