CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 73021 | prEN ISO 10993-3 rev | Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive and developmental toxicity | Izstrādē |
| 9485 | - | Biological evaluation of medical devices - Glutaraldehyde and formaldehyde residuals | Izstrādē |
| 80887 | prEN ISO 10993-4 rev | Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood | Izstrādē |
| 80886 | prEN ISO 22442-3 rev | Medical devices utilizing animal tissues and their derivatives — Part 3: Validation of the elimination and/or inactivation of viruses and transmissible spongiform encephalopathy (TSE) agents | Izstrādē |
| 80889 | prEN ISO 10993-14 rev | Biological evaluation of medical devices — Part 14: Identification and quantification of degradation products from ceramics | Izstrādē |
| 40814 | prEN ISO 10993-5 rev | Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009) | Izstrādē |
| 78992 | prEN ISO 10993-2 | Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO/DIS 10993-2:2024) | 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 |
| 40661 | prEN ISO 10993-7 rev | Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals | Izstrādē |
| 31980 | prEN ISO 10993-5 | Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:1999) | Izstrādē |
Displaying 1-10 of 195 results.