CEN/CLC/TC 3
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 69482 | EN ISO 15223-1:2016/FprA11 | Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements (ISO 15223-1:2016) | Izstrādē |
| 69481 | LVS EN ISO 13485:2016/A11:2021 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) | Standarts spēkā |
| 69481 | EN ISO 13485:2016/A11:2021 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) | Standarts spēkā |
| 68576 | LVS CEN ISO/TR 24971:2020 | Medical devices - Guidance on the application of ISO 14971 (ISO/TR 24971:2020) | Standarts spēkā |
| 68576 | CEN ISO/TR 24971:2020 | Medical devices - Guidance on the application of ISO 14971 (ISO/TR 24971:2020) | Standarts spēkā |
| 68559 | LVS EN ISO 15223-1:2021 | Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements (ISO 15223-1:2021) | Standarts spēkā |
| 68559 | EN ISO 15223-1:2021 | Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements (ISO 15223-1:2021) | Standarts spēkā |
| 67368 | EN ISO 20417:2021 | Medical devices - Information to be supplied by the manufacturer (ISO 20417:2021, Corrected version 2021-12) | Atcelts |
| 67368 | LVS EN ISO 20417:2021 | Medical devices - Information to be supplied by the manufacturer (ISO 20417:2021,Ccorrected version 2021-12) | Standarts spēkā |
| 66700 | LVS EN ISO 13485:2016/AC:2018 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) | Standarts spēkā |
Displaying 31-40 of 144 results.