CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 32766 | EN ISO 10993-12:2012 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO/DIS 10993-12:2010) | Atcelts |
| 33857 | EN ISO 10993-7:2008/AC:2009 | Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals - Technical Corrigendum 1 (ISO 10993-7:2008/Cor 1:2009) | Atcelts |
| 32007 | EN ISO 10993-11:2009 | Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006) | 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 |
| 21797 | EN ISO 10993-11:2006 | Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006) | Atcelts |
| 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 |
| 22132 | LVS EN ISO 10993-2:2006 | Biological evaluation of medical devices - Part 2: Animal welfare requirements | Atcelts |
Displaying 121-130 of 198 results.