ISO 18113-2:2022

In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2: In vitro diagnostic reagents for professional use

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Dispositifs médicaux de diagnostic in vitro — Informations fournies par le fabricant (étiquetage) — Partie 2: Réactifs de diagnostic in vitro à usage professionnel

Languages: In English

Type: standard

ICS groups: 11.100.10 In vitro diagnostic test systems

Technical commitee: ISO/TC 212/WG 3 In vitro diagnostic products

Registred: 06.10.2022.
In force: 06.10.2022.

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