CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 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 |
| 31981 | EN ISO 10993-9:2009 | Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:1999) | 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 |
| 9496 | EN ISO 10993-4:2002 | Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2002) | Atcelts |
| 9494 | EN ISO 10993-16:1997 | Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:1997) | Atcelts |
Displaying 101-110 of 195 results.