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Standard [CURRENT]

ISO 18113-1:2022-10

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

German title
In-vitro-Diagnostika - Bereitstellung von Informationen durch den Hersteller (Kennzeichnung) - Teil 1: Begriffe und allgemeine Anforderungen
Publication date
2022-10
Original language
English
Pages
53

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Publication date
2022-10
Original language
English
Pages
53

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Content
ICS
01.040.11, 11.100.10
Replacement amendments

This document replaces ISO 18113-1:2009-12 .

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