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Standard [WITHDRAWN]

DIN EN ISO 18113-4:2013-01

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009); German version EN ISO 18113-4:2011

German title
In-vitro-Diagnostika - Bereitstellung von Informationen durch den Hersteller - Teil 4: Reagenzien für in-vitro-diagnostische Untersuchungen zur Eigenanwendung (ISO 18113-4:2009); Deutsche Fassung EN ISO 18113-4:2011
Publication date
2013-01
Original language
German
Pages
20

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Publication date
2013-01
Original language
German
Pages
20
DOI
https://dx.doi.org/10.31030/1923433

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Overview

This part of ISO 18113 specifies requirements for information supplied by the manufacturer of in vitro diagnostic reagents for self-testing. This part of ISO 18113 also applies to information supplied by the manufacturers of calibrators and control materials intended for use with in vitro diagnostic medical devices for self-testing. This part of ISO 18113 can also be applied to accessories. This part of ISO 18113 applies to the labels for outer and immediate containers and to the instructions for use. This part of ISO 18113 does not apply to: a) IVD instruments or equipment; b) IVD reagents for professional use.

Content
ICS
11.100.10
DOI
https://dx.doi.org/10.31030/1923433
Replacement amendments

This document replaces DIN EN ISO 18113-4:2010-05 .

This document has been replaced by: DIN EN ISO 18113-4:2024-10 .

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