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BSI BS EN ISO 18113-3:2024

In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling) -- In vitro diagnostic instruments for professional use
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BSI BS EN ISO 18113-3:2024

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

PUBLISH DATE 2024
PAGES 26
BSI BS EN ISO 18113-3:2024
This document specifies requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) instruments intended for professional use. This document also applies to apparatus and equipment intended to be used with IVD instruments for professional use. This document can also be applicable to accessories. This document does not apply to: a) instructions for instrument servicing or repair; b) IVD reagents, including calibrators and control materials for use in control of the reagent; c) IVD instruments for self-testing.
SDO BSI: British Standards Institution
Document Number ISO 18113-3
Publication Date June 12, 2024
Language en - English
Page Count 26
Revision Level
Supercedes
Committee CH/212
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