Standarta informācija
ISO 18113-3:2022
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use
French
Dispositifs médicaux de diagnostic in vitro — Informations fournies par le fabricant (étiquetage) — Partie 3: Instruments 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.