CEN/CLC/TC 3
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 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 |
| 64226 | EN ISO 80369-3:2016/prA1 | Small-bore connectors for liquids and gases in healthcare applications - Part 3: Connectors for enteral applications - Amendment 1 (ISO 80369-3:2016/DAmd 1:2017) | Izstrādē |
| 32009 | prEN ISO 15225 rev | Nomenclature - Specification for a nomenclature system for medical devices for the purpose of regulatory data exchange (ISO 15225:2000) | Izstrādē |
| 32010 | EN 20594-1:1993/prA2 | Conical fittings with a 6% (Luer) taper for syringes, needles and certain other medical equipment - Part 1: General requirements (ISO 594-1:1986) | Izstrādē |
| 70256 | EN ISO 80369-7:2021 | Small-bore connectors for liquids and gases in healthcare applications - Part 7: Connectors with 6 % (Luer) taper for intravascular or hypodermic applications (ISO/DIS 80369-7:2019) | 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 |
| 80075 | FprCEN ISO/TS 24971-2 | Medical devices - Guidance on the application of ISO 14971 - Part 2: Machine learning in artificial intelligence (ISO/DTS 24971-2:2025) | Izstrādē |
| 77025 | prEN ISO 18250-7 | Medical devices — Connectors for reservoir delivery systems for healthcare applications — Part 7: Connectors for intravascular infusion | Izstrādē |
| 81836 | prCEN ISO/TS 23485 | Medical Devices -- Quality management systems -- Guideline for the application of ISO 13485:2016 | Izstrādē |
| 66700 | EN ISO 13485:2016/AC:2018 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) | Izstrādē |
Displaying 21-30 of 141 results.