CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 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 10993-1:2025) | Standarts spēkā |
| 25795 | EN ISO 22442-3:2007 | 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 (ISO 22442-3:2007) | Standarts spēkā |
| 65727 | EN ISO 10993-4:2017 | Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017) | Standarts spēkā |
| 65481 | EN ISO 22442-2:2020 | Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO 22442-2:2020) | Standarts spēkā |
| 77391 | EN ISO 10993-6:2026 | Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2026) | Standarts spēkā |
| 77182 | LVS EN ISO 14155:2026 | Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2026) | |
| 77391 | LVS EN ISO 10993-6:2026 | Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2026) | |
| 75885 | LVS EN ISO 10993-7:2026 | Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2026) |
Displaying 191-198 of 198 results.