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 |
| 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 |
| 45367 | ISO 10993-16:2010 | Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachables | Atcelts |
| 18967 | ISO 10993-7:1995 | Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals | Atcelts |
| 18966 | ISO 10993-6:1994 | Biological evaluation of medical devices — Part 6: Tests for local effects after implantation | Atcelts |
| 40884 | ISO 10993-10:2010 | Biological evaluation of medical devices — Part 10: Tests for irritation and skin sensitization | Atcelts |
| 26212 | ISO 10993-9:1999 | Biological evaluation of medical devices — Part 9: Framework for identification and quantification of potential degradation products | Atcelts |
| 33364 | ISO 10993-10:2002 | Biological evaluation of medical devices — Part 10: Tests for irritation and delayed-type hypersensitivity | Atcelts |
| 25333 | ISO 10993-1:1997 | Biological evaluation of medical devices — Part 1: Evaluation and testing | Atcelts |
Displaying 61-70 of 154 results.