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Norm
ISO 18113-1:2009
Issue date: 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...
Withdrawn: 2022 10 06
Publisher:
International Organization for Standardization
Format:
Digital | 49 Pages
Language:
English
Currently valid:
ICS
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
Issue date :
2022 10 06
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions, and general requirements
