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Norm
ISO 18113-2:2009
Issue date: 2009 12 09
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2: In vitro diagnostic reagents for professional use
ISO 18113-2:2009 specifies requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) reagents for professional use.
ISO 18113-2:2009 also app...
Withdrawn: 2022 10 06
Publisher:
International Organization for Standardization
Format:
Digital | 10 Pages
Language:
English
Currently valid:
ICS
ISO 18113-2:2009 specifies requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) reagents for professional use.
ISO 18113-2:2009 also applies to information supplied by the manufacturer with calibrators and control materials intended for use with IVD medical devices for professional use.
ISO 18113-2:2009 can also be applied to accessories.
ISO 18113-2:2009 applies to the labels for outer and immediate containers and to the instructions for use.
ISO 18113-2:2022
2022 10 06
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2:...
Norm
ISO 18113-2:2009
2009 12 09
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2:...
Norm
↖
Norm
Issue date :
2022 10 06
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2: In vitro diagnostic reagents for professional use
