ISO/TC 194
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 88206 | ISO/DIS 10993-16 | Biological evaluation of medical devices — Part 16: Toxicokinetic evaluation for degradation products and leachables | Izstrādē |
| 88205 | ISO 10993-12:2021/Amd 1:2025 | Biological evaluation of medical devices — Part 12: Sample preparation and reference materials — Amendment 1 | Standarts spēkā |
| 88204 | ISO/AWI TR 24850 | Sources of hazard information for medical device constituents | Izstrādē |
| 88203 | ISO/PWI TS 24830 | Application of in-silico/read-across approaches for identifying a medical device constituent analogue | Izstrādē |
| 88202 | ISO/AWI TS 21726 | Biological evaluation of medical devices — Application of the threshold of toxicological concern (TTC) for assessing biocompatibility of medical device constituents | Izstrādē |
| 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/FDIS 10993-3 | Biological evaluation of medical devices — Part 3: Evaluation of genotoxicity, carcinogenicity, reproductive toxicity, and developmental toxicity | Izstrādē |
| 86868 | ISO/DIS 21762 | Medical devices utilizing non-viable human materials — Risk management | Aptauja |
| 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 |
Displaying 21-30 of 154 results.