CEN/CLC/TC 3
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
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 |
32013 | prEN ISO 13485 rev | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003) | Izstrādē |
77231 | EN ISO 15223-1:2021/prA1 | 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/DAM 1:2024) | 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 |
81349 | prCEN ISO/TR 20416 rev | Medical devices — Post-market surveillance for manufacturers | Izstrādē |
32011 | EN 1707:1996/prA1 | Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment - Lock fittings | Izstrādē |
70256 | EN ISO 80369-7:2021 | Small-bore connectors for liquids and gases in healthcare applications - Part 7: Connectors for intravascular or hypodermic applications (ISO 80369-7:2021) | Izstrādē |
80075 | prCEN ISO/TS 24971-2 | Medical devices — Guidance on the application of ISO 14971 — Part 2: Machine learning in artificial intelligence | Izstrādē |
66179 | prEN ISO 80369-3 rev | Small-bore connectors for liquids and gases in healthcare applications - Part 3: Connectors for enteral applications (ISO 80369-3:2016) | Izstrādē |
66700 | EN ISO 13485:2016/AC:2018 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) | Izstrādē |
Displaying 121-130 of 140 results.