CEN/CLC/TC 3
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 71616 | EN ISO 80369-3:2016/A1:2022 | Small-bore connectors for liquids and gases in healthcare applications - Part 3: Connectors for enteral applications - Amendment 1 (ISO 80369-3:2016/Amd 1:2019) | 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 |
| 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 |
| 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 |
| 24165 | prEN ISO 14971-B | Medical devices -- Application of risk management to medical devices -- Part B: In vitro diagnostic medical devices | Izstrādē |
| 80075 | prCEN ISO/TS 24971-2 | Medical devices — Guidance on the application of ISO 14971 — Part 2: Machine learning in artificial intelligence | Izstrādē |
| 68576 | CEN ISO/TR 24971:2020 | Medical devices - Guidance on the application of ISO 14971 (ISO/TR 24971:2020) | Izstrādē |
| 66700 | EN ISO 13485:2016/AC:2018 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) | Izstrādē |
| 32013 | prEN ISO 13485 rev | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003) | 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 |
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