CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 27092 | LVS EN ISO 10993-1:2010 | Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2009) | Atcelts |
| 9489 | LVS EN ISO 10993-15:2003 | Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys | Atcelts |
| 9475 | LVS EN 30993-3:1993 | Biological evalution of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity | Atcelts |
| 27092 | EN ISO 10993-1:2009 | Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2009) | Atcelts |
| 9477 | EN ISO 10993-10:1995 | Biological evaluation of medical devices - Part 10: Tests for irritation and sensitization (ISO 10993-10:1995) | Atcelts |
| 9481 | EN ISO 10993-7:1995 | Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:1995) | Atcelts |
| 9480 | EN 30993-6:1994 | Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:1994) | Atcelts |
| 9497 | EN ISO 10993-5:1999 | Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:1999) | Atcelts |
| 9472 | EN 30993-5:1994 | Biological evaluation of medical devices - Part 5: Tests for cytotoxicity - in vitro methods (ISO 10993-5:1992) | Atcelts |
| 9499 | EN ISO 10993-17:2002 | Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002) | Atcelts |
Displaying 161-170 of 194 results.