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Norm
ÖNORM EN 376
Issue date: 2002 05 01
Information supplied by the manufacturer with in vitro diagnostic reagents for self-testing
This European Standard specifies the requirements for the information supplied by the manufacturer of in vitro
diagnostic reagents for use in self-testing including reag...
Withdrawn: 2010 04 15
§ Legal References
Publisher:
Austrian Standards International
Format:
Digital | 14 Pages
Language:
German
| English
Currently valid:
Optionally co-design standards:
ICS
This European Standard specifies the requirements for the information supplied by the manufacturer of in vitro
diagnostic reagents for use in self-testing including reagent products, calibrators, control materials and kits, which
hereafter are called IVD reagents.
NOTE This standard can also be applied to accessories.
ÖNORM EN ISO 18113-4
2024 10 01
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4:...
Norm
ÖNORM EN ISO 18113-4
2012 12 01
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4:...
Norm
ÖNORM EN ISO 18113-4
2010 04 15
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4:...
Norm
ÖNORM EN 376
2002 05 01
Information supplied by the manufacturer with in vitro diagnostic reagents for self-testing
Norm
↖
ÖNORM EN 376
1993 03 01
In vitro diagnostic systems - Requirements for labelling of in vitro diagnostic reagents for self-te...
Norm
Norm
Issue date :
1992 11 12
SI units and recommendations for the use of their multiples and of certain other units
Norm
Issue date :
2010 04 15
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009)
