CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 77391 | prEN ISO 10993-6 | Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO/DIS 10993-6:2024) | Izstrādē |
| 9483 | - | Biological evaluation of medical devices - Methods of testing for degradation products | Izstrādē |
| 75596 | FprEN ISO 10993-1 | 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 | prEN ISO 10993-7 | Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO/DIS 10993-7:2024) | Izstrādē |
| 73021 | prEN ISO 10993-3 rev | Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive and developmental toxicity | Izstrādē |
| 40814 | prEN ISO 10993-5 rev | Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009) | Izstrādē |
| 80888 | prEN ISO 10993-13 rev | Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devices | Izstrādē |
| 9485 | - | Biological evaluation of medical devices - Glutaraldehyde and formaldehyde residuals | Izstrādē |
| 80889 | prEN ISO 10993-14 rev | Biological evaluation of medical devices — Part 14: Identification and quantification of degradation products from ceramics | Izstrādē |
| 79217 | EN ISO 10993-7:2008/prA11 | Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals | Izstrādē |
Displaying 11-20 of 192 results.