ISO/TC 194
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 31723 | ISO 14155-1:2003 | Clinical investigation of medical devices for human subjects — Part 1: General requirements | Atcelts |
| 18966 | ISO 10993-6:1994 | Biological evaluation of medical devices — Part 6: Tests for local effects after implantation | Atcelts |
| 18967 | ISO 10993-7:1995 | Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals | Atcelts |
| 88199 | ISO/DIS 10993-3 | Biological evaluation of medical devices — Part 3: Evaluation of genotoxicity, carcinogenicity, reproductive toxicity, and developmental toxicity | Aptauja |
| 86799 | ISO/DIS 10993-11 | Biological evaluation of medical devices — Part 11: Tests for systemic toxicity | Aptauja |
| 55614 | ISO 10993-3:2014 | Biological evaluation of medical devices — Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity | Standarts spēkā |
| 63448 | ISO 10993-4:2017 | Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood | Standarts spēkā |
| 71862 | ISO/TR 10993-55:2023 | Biological evaluation of medical devices — Part 55: Interlaboratory study on cytotoxicity | Standarts spēkā |
| 75769 | ISO 10993-12:2021 | Biological evaluation of medical devices — Part 12: Sample preparation and reference materials | Standarts spēkā |
| 75323 | ISO 10993-17:2023 | Biological evaluation of medical devices — Part 17: Toxicological risk assessment of medical device constituents | Standarts spēkā |
Displaying 111-120 of 146 results.