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EU - 2002/364/EC

Commission Decision on Common Technical Specifications for in Vitro-Diagnostic Medical Devices

active, Most Current
Organization: EU
Publication Date: 7 May 2002
Status: active
Page Count: 14

Document History

2002/364/EC
May 7, 2002
Commission Decision on Common Technical Specifications for in Vitro-Diagnostic Medical Devices
A description is not available for this item.

References

This document is referenced by:
ISO 18113-1 FRENCH - Dispositifs médicaux de diagnostic in vitro - Informations fournies par le fabricant (étiquetage) - Partie 1: Termes, définitions et exigences générales
Published by ISO on December 15, 2009
A description is not available for this item.
This document is referenced by:
18113-1 - In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions, and general requirements
Published by ISO on October 1, 2022
This document defines concepts, establishes general principles, and specifies essential requirements for information supplied by the manufacturer of IVD medical devices. This document does not...
This document is referenced by:
DIN EN ISO 18113-1 - In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)
Published by DIN on January 1, 2013
This part of ISO 18113 defines concepts, establishes general principles and specifies essential requirements for information supplied by the manufacturer of IVD medical devices. This part of ISO...
This document is referenced by:
DIN EN ISO 18113-1 - In-vitro-Diagnostika - Bereitstellung von Informationen durch den Hersteller - Teil 1: Begriffe und allgemeine Anforderungen (ISO 18113-1:2009); Deutsche Fassung EN ISO 18113-1:2011
Published by DIN on January 1, 2013
Dieser Teil von ISO 18113 definiert Konzepte, stellt allgemeine Prinzipien auf und legt wesentliche Anforderungen an die durch den Hersteller von In-vitro-Diagnostika bereitzustellenden Informationen...
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