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In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009); German version EN ISO 18113-3:2011

Standard [WITHDRAWN]

DIN EN ISO 18113-3:2013-01

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009); German version EN ISO 18113-3:2011

German title
In-vitro-Diagnostika - Bereitstellung von Informationen durch den Hersteller - Teil 3: Geräte für in-vitro-diagnostische Untersuchungen zum Gebrauch durch Fachpersonal (ISO 18113-3:2009); Deutsche Fassung EN ISO 18113-3:2011
Publication date
2013-01
Original language
German
Pages
18

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Publication date
2013-01
Original language
German
Pages
18
DOI
https://dx.doi.org/10.31030/1923432

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Overview

The revised standard includes a more precise version of Annex ZA, which presents the relationship between the European Standard and the essential requirements of the EU Directive 98/79/EC on in vitro diagnostic medical devices.

Content

ICS

11.100.10

DOI

https://dx.doi.org/10.31030/1923432
Replacement amendments

This document replaces DIN EN ISO 18113-3:2010-05 .

This document has been replaced by: DIN EN ISO 18113-3:2024-10 .

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