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Standard [AVAILABLE PRE-PUBLICATION]

DIN EN ISO 18113-3:2024-10

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2022); German version EN ISO 18113-3:2024

German title
In-vitro-Diagnostika - Bereitstellung von Informationen durch den Hersteller (Kennzeichnung) - Teil 3: Geräte für in-vitro-diagnostische Untersuchungen zum Gebrauch durch Fachpersonal (ISO 18113-3:2022); Deutsche Fassung EN ISO 18113-3:2024
Publication date
2024-10
Original language
German
Pages
25

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Publication date
2024-10
Original language
German
Pages
25
DOI
https://dx.doi.org/10.31030/3370949

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Content
ICS
11.100.10
DOI
https://dx.doi.org/10.31030/3370949
Replacement amendments

This document replaces DIN EN ISO 18113-3:2013-01 .

And replaced by 2024-10 for:: DIN EN ISO 18113-3:2013-01 , DIN EN ISO 18113-3:2021-09 .

Document timeline
PRE-PUBLISHED
2024-10

Standard [AVAILABLE PRE-PUBLICATION]

DIN EN ISO 18113-3:2024-10
Drafts
2021-09 - 2024-10

Draft standard

DIN EN ISO 18113-3:2021-09
intended to be withdrawn
2013-01 - 2024-10

Standard

DIN EN ISO 18113-3:2013-01

Cooperation at DIN

Relationship to other standards
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