ISO/TC 194
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 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 |
| 90744 | ISO/DIS 10993-4 | Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood | Aptauja |
| 22695 | ISO 10993-16:1997 | Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachables | Atcelts |
| 22692 | ISO 10993-13:1998 | Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devices | Atcelts |
| 59992 | ISO 14155:2011/Cor 1:2011 | Clinical investigation of medical devices for human subjects — Good clinical practice — Technical Corrigendum 1 | Atcelts |
| 65052 | ISO/TR 10993-33:2015 | Biological evaluation of medical devices — Part 33: Guidance on tests to evaluate genotoxicity — Supplement to ISO 10993-3 | Atcelts |
| 31723 | ISO 14155-1:2003 | Clinical investigation of medical devices for human subjects — Part 1: General requirements | Atcelts |
| 68936 | ISO 10993-1:2018 | Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management process | Atcelts |
| 72766 | ISO 10993-7:2008/Amd 1:2019 | Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals — Amendment 1: Applicability of allowable limits for neonates and infants | Atcelts |
Displaying 31-40 of 159 results.