CEN/CLC/TC 3
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 38201 | LVS EN ISO 13485:2012 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003) | |
| 76512 | LVS EN ISO 80369-6:2025 | Small bore connectors for liquids and gases in healthcare applications - Part 6: Connectors for neural applications (ISO 80369-6:2025) | 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 |
| 73006 | LVS EN ISO 80369-2:2024 | Small-bore connectors for liquids and gases in healthcare applications - Part 2: Connectors for respiratory applications (ISO 80369-2:2024, Corrected version 2025-06) | 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 |
| 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 |
| 77231 | LVS EN ISO 15223-1:2021/A1:2025 | Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements - Amendment 1: Addition of defined term for authorized representative and modified EC REP symbol to not be country or region specific (ISO 15223 1:2021/Amd 1:2025) | Standarts spēkā |
| 67368 | LVS EN ISO 20417:2021 | Medical devices - Information to be supplied by the manufacturer (ISO 20417:2021,Ccorrected version 2021-12) | Standarts spēkā |
| 66261 | LVS CEN ISO/TR 20416:2020 | Medical devices - Post-market surveillance for manufacturers (ISO/TR 20416:2020) | Standarts spēkā |
| 75110 | LVS EN ISO 14971:2020/A11:2022 | Medical devices - Application of risk management to medical devices (ISO 14971:2019) | Standarts spēkā |
Displaying 11-20 of 144 results.