CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 69998 | LVS EN ISO 10993-2:2023 | Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:2022) | Standarts spēkā |
| 73021 | prEN ISO 10993-3 rev | Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive and developmental toxicity | Izstrādē |
| 74131 | EN ISO 10993-18:2020/A1:2023 | Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process - Amendment 1: Determination of the uncertainty factor (ISO 10993-18:2020/Amd 1:2022) | Standarts spēkā |
| 74131 | LVS EN ISO 10993-18:2020/A1:2023 | Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process - Amendment 1: Determination of the uncertainty factor (ISO 10993-18:2020/Amd 1:2022) | Standarts spēkā |
| 75596 | EN ISO 10993-1:2025 | Biological evaluation of medical devices - Part 1: Requirements and general principles for the evaluation of biological safety within a risk management process (ISO/FDIS 10993-1:2025) | Izstrādē |
| 75885 | FprEN ISO 10993-7 | Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO/FDIS 10993-7:2025) | Izstrādē |
| 76054 | prEN ISO 8250 | Cleanliness of medical devices -- Process design and test methods | Izstrādē |
| 77182 | FprEN ISO 14155 | Clinical investigation of medical devices for human subjects - Good clinical practice (ISO/FDIS 14155:2025) | Izstrādē |
| 77335 | prEN ISO 18969 | Clinical evaluation of medical devices | Izstrādē |
| 77391 | FprEN ISO 10993-6 | Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO/FDIS 10993-6:2025) | Izstrādē |
Displaying 161-170 of 192 results.