CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 32008 | LVS EN ISO 10993-12:2009 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2007) | 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 |
| 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 |
| 9487 | LVS EN ISO 10993-13:2000 | Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices | Atcelts |
| 23724 | LVS EN ISO 10993-10:2003 /A1:2006 | Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity | Atcelts |
| 32005 | LVS EN ISO 10993-1:2009 | Biological evaluation of medical devices - Part 1: Evaluation and testing (ISO 10993-1:2003) | Atcelts |
| 27050 | LVS EN ISO 10993-9:2010 | Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:2009) | Atcelts |
| 32006 | LVS EN ISO 10993-6:2009 | Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2007) | Atcelts |
| 9481 | LVS EN ISO 10993-7:2000 | Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals | Atcelts |
| 31999 | LVS EN ISO 10993-13:2009 | Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:1998) | Atcelts |
Displaying 41-50 of 194 results.