ISO/TC 212/WG 3
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 79866 | ISO 18113-1:2022 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions, and general requirements | 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 |
| 79870 | ISO 18113-5:2022 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 5: In vitro diagnostic instruments for self-testing | 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 |
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