ISO/TC 194
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 88201 | ISO 10993-17:2023/Amd 1:2025 | Biological evaluation of medical devices — Part 17: Toxicological risk assessment of medical device constituents — Amendment 1 | Standarts spēkā |
| 88200 | ISO 10993-23:2021/Amd 1:2025 | Biological evaluation of medical devices — Part 23: Tests for irritation — Amendment 1: Additional in vitro reconstructed human epidermis models | Standarts spēkā |
| 88199 | ISO 10993-3:2026 | Biological evaluation of medical devices — Part 3: Evaluation of genotoxicity, carcinogenicity, reproductive toxicity and developmental toxicity | Standarts spēkā |
| 86868 | ISO/FDIS 21762 | Medical devices utilizing non-viable human materials — Application of risk management | Izstrādē |
| 86862 | ISO 10993-4:2017/Amd 1:2025 | Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood — Amendment 1 | Standarts spēkā |
| 86799 | ISO/DIS 10993-11.2 | Biological evaluation of medical devices — Part 11: Tests for systemic toxicity | Aptauja slēgta |
| 86796 | ISO/AWI 10993-4 | Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood — Amendment 1 | Izstrādē |
| 86248 | ISO/PWI TS 10993-22 | Biological evaluation of medical devices — Part 22: Guidance on nanomaterials | Izstrādē |
| 86247 | ISO/CD TS 20324 | Generation of medical device extracts for chemical analysis to support toxicological risk assessment | Izstrādē |
| 86246 | ISO/DIS 10993-2 | Biological evaluation of medical devices — Part 2: Animal welfare requirements | Izstrādē |
Displaying 31-40 of 159 results.