CEN/CLC/TC 3
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 66261 | CEN ISO/TR 20416:2020 | Medical devices - Post-market surveillance for manufacturers (ISO/DTR 20416:2020) | Standarts spēkā |
| 39364 | EN ISO 80369-3:2016 | Small-bore connectors for liquids and gases in healthcare applications - Part 3: Connectors for enteral applications (ISO/IEC/DIS 80369-3:2013) | Standarts spēkā |
| 66261 | LVS CEN ISO/TR 20416:2020 | Medical devices - Post-market surveillance for manufacturers (ISO/TR 20416:2020) | Standarts spēkā |
| 79260 | EN ISO 20417:2026 | Medical devices - Information to be supplied by the manufacturer (ISO 20417:2026) | Standarts spēkā |
| 69481 | LVS EN ISO 13485:2016/A11:2021 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) | Standarts spēkā |
| 39364 | LVS EN ISO 80369-3:2016 | Small-bore connectors for liquids and gases in healthcare applications - Part 3: Connectors for enteral applications (ISO 80369-3:2016) | Standarts spēkā |
| 73639 | LVS EN ISO 80369-20:2024 | Small-bore connectors for liquids and gases in healthcare applications - Part 20: Common test methods (ISO 80369‑20:2024) | 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 |
| 63920 | LVS EN ISO 14971:2020 | Medical devices - Application of risk management to medical devices (ISO 14971:2019) | Standarts spēkā |
| 69481 | EN ISO 13485:2016/A11:2021 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) | Standarts spēkā |
Displaying 41-50 of 144 results.