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Norm
ÖNORM EN 375
Issue date: 2001 04 01
Information supplied by the manufacturer with in vitro diagnostic reagents for professional use
This standard specifies the requirements for the information supplied by the manufacturer of in vitro diagnostic
reagents including reagent products, calibrators, contro...
Withdrawn: 2010 04 15
§ Legal References
Publisher:
Austrian Standards International
Format:
Digital | 17 Pages
Language:
German
| English
Currently valid:
Optionally co-design standards:
ICS
This standard specifies the requirements for the information supplied by the manufacturer of in vitro diagnostic
reagents including reagent products, calibrators, control materials and kits for professional use, which hereafter are
called IVD reagents.
NOTE This standard can also be applied to accessories.
ÖNORM EN ISO 18113-2
2024 10 01
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2:...
Norm
ÖNORM EN ISO 18113-2
2012 12 01
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2:...
Norm
ÖNORM EN ISO 18113-2
2010 04 15
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2:...
Norm
ÖNORM EN 375
2001 04 01
Information supplied by the manufacturer with in vitro diagnostic reagents for professional use
Norm
↖
ÖNORM EN 375
1993 03 01
In vitro diagnostic systems - Requirements for labelling of in vitro diagnostic reagents for profess...
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 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009)
