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ISO 18113-3:2009

In vitro diagnostic medical devices -- Information supplied by the manufacturer (labelling) -- Part 3: In vitro diagnostic instruments for professional use

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Kehtetu alates 06.10.2022
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Kuupäev
Tüüp
Nimetus
06.10.2022
Põhitekst
09.12.2009
Põhitekst
ISO 18113-3:2009 specifies requirements for information supplied by the manufacturer of in vitro dignostic (IVD) instruments for professional use.
ISO 18113-3:2009 also applies to apparatus and equipment intended to be used with IVD instruments for professional use.
ISO 18113-3:2009 can also be applied to accessories, where appropriate.
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ISO 18113-1:2009

In vitro diagnostic medical devices -- Information supplied by the manufacturer (labelling) -- Part 1: Terms, definitions and general requirements
Kehtetu alates 06.10.2022