ISO/TC 194
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 23955 | ISO 10993-17:2002 | Biological evaluation of medical devices — Part 17: Establishment of allowable limits for leachable substances | Atcelts |
| 25333 | ISO 10993-1:1997 | Biological evaluation of medical devices — Part 1: Evaluation and testing | Atcelts |
| 26211 | ISO 10993-5:1999 | Biological evaluation of medical devices — Part 5: Tests for in vitro cytotoxicity | Atcelts |
| 26212 | ISO 10993-9:1999 | Biological evaluation of medical devices — Part 9: Framework for identification and quantification of potential degradation products | Atcelts |
| 27499 | ISO/NP 10993-4 | Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood | Izstrādē |
| 31481 | ISO/DIS 10993-18 | Biological evaluation of medical devices — Part 18: Chemical characterization of materials | Izstrādē |
| 31723 | ISO 14155-1:2003 | Clinical investigation of medical devices for human subjects — Part 1: General requirements | Atcelts |
| 32086 | ISO 10993-4:2002 | Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood | Atcelts |
| 32162 | ISO 10993-3:2003 | Biological evaluation of medical devices — Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity | Atcelts |
| 32217 | ISO 14155-2:2003 | Clinical investigation of medical devices for human subjects — Part 2: Clinical investigation plans | Atcelts |
Displaying 21-30 of 154 results.