ISO 18113-3:2009Withdrawn

In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use

Dispositifs médicaux de diagnostic in vitro — Informations fournies par le fabricant (étiquetage) — Partie 3: Instruments de diagnostic in vitro à usage professionnel

This edition has been replaced by ISO 18113-3:2022.

Abstract / scope

ISO 18113-3:2009 specifies requirements for information supplied by the manufacturer of in vitro dignostic (IVD) instruments for professional use.

ISO 18113-3:2009 also applies to apparatus and equipment intended to be used with IVD instruments for professional use.

ISO 18113-3:2009 can also be applied to accessories, where appropriate.

Life cycle

Replaced by

ISO 18113-3:2022PublishedIn vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional useInternational Standard · Published 6 Oct 2022 · ISO/TC 212