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Norm

ISO 18113-1:2009

Ausgabedatum: 2009 12 09

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

ISO 18113-1:2009 defines concepts, establishes general principles and specifies essential requirements for information supplied by the manufacturer of in vitro diagnostic...
Weiterlesen
ZURÜCKGEZOGEN : 2022 10 06
Herausgeber:
International Organization for Standardization
Format:
Digital | 49 Seiten
Sprache:
Englisch
Aktuell Gültig:
ISO 18113-1:2022:2022 10 06
ICS
11.100.10
Fachgebiete
Healthcare, Laboratory medicine, In vitro diagnostic test systems

ISO 18113-1:2009 defines concepts, establishes general principles and specifies essential requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) medical devices.

ISO 18113-1:2022
2022 10 06
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1:...
Norm
ISO 18113-1:2009
2009 12 09
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1:...
Norm
↖
Norm
ISO 18113-1:2022
Ausgabedatum : 2022 10 06
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions, and general requirements