CEN/CLC/TC 3
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 31253 | prEN ISO 80369-2 | Small bore connectors for liquids and gases in healthcare applications - Part 2: Connectors for breathing systems and driving gases applications (ISO/DIS 80369-2:2015) | Izstrādē |
| 72189 | - | Guidance on the relationship between CEN ISO TR 20146: 2019 (Medical devices — Post-market surveillance for manufacturers) and European Medical Devices Regulation and In Vitro Diagnostic Medical Devices Regulation | Izstrādē |
| 65274 | EN ISO 80369-3:2016/prA1 | Small-bore connectors for liquids and gases in healthcare applications - Part 3: Connectors for enteral applications - Amendment 1 | Izstrādē |
| 24165 | prEN ISO 14971-B | Medical devices -- Application of risk management to medical devices -- Part B: In vitro diagnostic medical devices | Izstrādē |
| 80075 | FprCEN ISO/TS 24971-2 | Medical devices - Guidance on the application of ISO 14971 - Part 2: Machine learning in artificial intelligence (ISO/DTS 24971-2:2026) | Izstrādē |
| 73733 | FprEN ISO 80369-1 | Small-bore connectors for liquids and gases in healthcare applications - Part 1: General requirements (ISO/FDIS 80369-1:2025) | Izstrādē |
| 18858 | CR 14060:2000 | Medical device traceability | Atcelts |
| 24868 | EN ISO 15225:2000/A2:2005 | Nomenclature - Specification for a nomenclature system for medical devices for the purpose of regulatory data exchange (ISO 15225:2000/Amd 1:2004) | Atcelts |
| 38595 | EN ISO 14971:2012 | Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01) | Atcelts |
| 64861 | LVS CEN/TR 17223:2018 | Guidance on the relationship between EN ISO 13485: 2016 (Medical devices - Quality management systems - Requirements for regulatory purposes) and European Medical Devices Regulation and In Vitro Diagnostic Medical Devices Regulation | Atcelts |
Displaying 21-30 of 142 results.