CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 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 |
| 60213 | EN ISO 22442-1:2015 | Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management (ISO 22442-1:2015) | Atcelts |
| 60214 | EN ISO 22442-2:2015 | Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO 22442-2:2015) | Atcelts |
| 35184 | EN ISO 10993-1:2009/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 |
| 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 |
| 9495 | EN ISO 10993-3:2003 | Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2003) | Atcelts |
| 9492 | EN ISO 10993-1:1997 | Biological evaluation of medical devices - Part 1: Evaluation and testing (ISO 10993-1:1997) | Atcelts |
| 40815 | EN ISO 10993-4:2017 | Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017) | Atcelts |
| 21140 | EN ISO 10993-12:2004 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2002) | Atcelts |
| 9478 | EN ISO 10993-11:1995 | Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:1993) | Atcelts |
Displaying 71-80 of 192 results.