ISO/TC 212/WG 3
| Reģistrācijas numurs (WIID) | Projekta Nr. | Nosaukums | Statuss |
|---|---|---|---|
| 79870 | ISO 18113-5:2022 | Dispositifs médicaux de diagnostic in vitro — Informations fournies par le fabricant (étiquetage) — Partie 5: Instruments de diagnostic in vitro destinés aux autodiagnostics | Standarts spēkā |
| 79869 | ISO 18113-4:2022 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 4: In vitro diagnostic reagents for self-testing | Standarts spēkā |
| 79868 | ISO 18113-3:2022 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use | Standarts spēkā |
| 79866 | ISO 18113-1:2022 | Dispositifs médicaux de diagnostic in vitro — Informations fournies par le fabricant (étiquetage) — Partie 1: Termes, définitions et exigences générales | Standarts spēkā |
| 79867 | ISO 18113-2:2022 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2: In vitro diagnostic reagents for professional use | Standarts spēkā |
Attēlo no 1. līdz 5. no pavisam 5 ieraksta(-iem).