CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 9479 | LVS EN 30993-4:1993 | Biological evalution of medical devices - Part 4: Selection of tests for interactions with blood | Atcelts |
| 9475 | LVS EN 30993-3:1993 | Biological evalution of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity | Atcelts |
| 9471 | LVS EN 30993-1:1994 | Biological evaluation of medical devices - Part 1: Guidance on selection of tests (ISO 10993-1:1992 + Technical Corrigendum 1:1992) | Atcelts |
| 78988 | FprEN ISO 10993-3 | Biological evaluation of medical devices - Part 3: Evaluation of genotoxicity, carcinogenicity, reproductive toxicity, and developmental toxicity (ISO/FDIS 10993-3:2026) | Izstrādē |
| 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 |
| 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 |
| 60214 | EN ISO 22442-2:2015 | Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO/FDIS 22442-2:2015) | Atcelts |
| 65480 | EN ISO 22442-1:2020 | Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management (ISO/DIS 22442-1:2018) | Standarts spēkā |
| 60213 | EN ISO 22442-1:2015 | Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management (ISO/FDIS 22442-1:2015) | Atcelts |
| 77182 | EN ISO 14155:2026 | Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2026) | Standarts spēkā |
Displaying 101-110 of 198 results.