CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 21140 | LVS EN ISO 10993-12:2005 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials | Atcelts |
| 9494 | LVS EN ISO 10993-16:1997 | Biological evalution of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables | 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 |
| 22132 | LVS EN ISO 10993-2:2006 | Biological evaluation of medical devices - Part 2: Animal welfare requirements | Atcelts |
| 79539 | EN ISO 14155:2020/A11:2024 | Clinical investigation of medical devices for human subjects - Good clinical practice | Atcelts |
| 40624 | LVS EN ISO 10993-10:2013 | Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO 10993-10:2010) | Atcelts |
| 32001 | LVS EN ISO 10993-15:2009 | Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000) | 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 |
| 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 |
| 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 |
Displaying 51-60 of 198 results.