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 |
| 78988 | prEN ISO 10993-3 | Biological evaluation of medical devices - Part 3: Evaluation of genotoxicity, carcinogenicity, reproductive toxicity, and developmental toxicity (ISO/DIS 10993-3:2025) | Izstrādē |
| 78992 | prEN ISO 10993-2 | Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO/DIS 10993-2:2024) | Izstrādē |
| 78991 | prEN ISO 10993-16 rev | Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables | Izstrādē |
| 80889 | prEN ISO 10993-14 rev | Biological evaluation of medical devices — Part 14: Identification and quantification of degradation products from ceramics | 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 |
| 77933 | prEN ISO 10993-11 | Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO/DIS 10993-11:2025) | Aptauja slēgta |
| 65481 | LVS EN ISO 22442-2:2021 | Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO 22442-2:2020) | Standarts spēkā |
| 65480 | LVS EN ISO 22442-1:2021 | Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management (ISO 22442-1:2020) | Standarts spēkā |
| 79539 | LVS EN ISO 14155:2020/A11:2024 | Clinical investigation of medical devices for human subjects - Good clinical practice | Standarts spēkā |
Displaying 11-20 of 192 results.