ISO 18113-1:2009
International Standard
Historical
·
Approved on
09 December 2009
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements
ISO 18113-1:2009 Files
English
49 Pages
Historical
OMR
87.25
ISO 18113-1:2009 Scope
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.
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