CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 9480 | EN 30993-6:1994 | Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:1994) | Atcelts |
| 9481 | EN ISO 10993-7:1995 | Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:1995) | Atcelts |
| 31981 | LVS 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 |
| 22598 | LVS EN ISO 10993-1:2003 | Biological evaluation of medical devices - Part 1: Evaluation and testing | 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 |
| 35184 | LVS EN ISO 10993-1:2010 /AC:2010 | Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process - Technical Corrigendum 1 (ISO 10993-1:2009/Cor 1:2010) | 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 |
| 31979 | LVS EN ISO 10993-4:2009 | Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2002, including Amd 1:2006) | Atcelts |
| 9496 | LVS EN ISO 10993-4:2003 | Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood | Atcelts |
| 32766 | LVS EN ISO 10993-12:2012 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012) | Atcelts |
Displaying 61-70 of 192 results.