BAS EN 375:2002
Information supplied by the manufacturer with in vitro diagnostic reagents for professional use
General Information
Status: Withdrawn
No. of pages: 16
Language: English
Edition: 1.
Adoption method: Endorsment
Publication date: 08.10.2002
Technical committee:
Directive:
98/79/EC, In vitro diagnostic medical devices;
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Abstract
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 reagents. Note: This standard can also be applied to accessories.
Lifecycle
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Original document and degree of correspondence
- EN 375:2001, identical