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 |
| 32217 | ISO 14155-2:2003 | Clinical investigation of medical devices for human subjects — Part 2: Clinical investigation plans | Atcelts |
| 18962 | ISO 10993-3:1992 | Biological evaluation of medical devices — Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity | Atcelts |
| 45557 | ISO 14155:2011 | Clinical investigation of medical devices for human subjects — Good clinical practice | Atcelts |
| 40384 | ISO 10993-12:2007 | Biological evaluation of medical devices — Part 12: Sample preparation and reference materials | Atcelts |
| 33364 | ISO 10993-10:2002 | Biological evaluation of medical devices — Part 10: Tests for irritation and delayed-type hypersensitivity | Atcelts |
| 39205 | ISO 10993-4:2002/Amd 1:2006 | Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood — Amendment 1 | Atcelts |
| 40884 | ISO 10993-10:2010 | Biological evaluation of medical devices — Part 10: Tests for irritation and skin sensitization | Atcelts |
| 35331 | ISO 10993-12:2002 | Biological evaluation of medical devices — Part 12: Sample preparation and reference materials | Atcelts |
| 26212 | ISO 10993-9:1999 | Biological evaluation of medical devices — Part 9: Framework for identification and quantification of potential degradation products | Atcelts |
Displaying 61-70 of 156 results.