CEN/CLC/TC 3
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 31995 | prEN ISO 14971 | Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01) | Izstrādē |
| 28643 | prEN 15546-2 | Small bore connectors for liquids and gases in healthcare applications - Part 2 - Connectors for respiratory applications | 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 |
| 39198 | EN 1041:2008/FprA1 | Information supplied by the manufacturer of medical devices | Izstrādē |
| 32011 | EN 1707:1996/prA1 | Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment - Lock fittings | Izstrādē |
| 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 |
| 77024 | prEN ISO 18250-6 | Medical devices — Connectors for reservoir delivery systems for healthcare applications — Part 6: Neural applications | Izstrādē |
| 77023 | prEN ISO 18250-3 | Medical devices — Connectors for reservoir delivery systems for healthcare applications — Part 3: Enteral applications | Izstrādē |
| 81836 | prCEN ISO/TS 23485 | Medical Devices -- Quality management systems -- Guideline for the application of ISO 13485:2016 | 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 |
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