CEN/TC 206
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
32003 | EN ISO 10993-17:2009 | Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002) | Atcelts |
40624 | EN ISO 10993-10:2013 | Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO 10993-10:2010) | Atcelts |
21801 | EN ISO 10993-6:2007 | Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2007) | Atcelts |
21797 | EN ISO 10993-11:2006 | Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006) | Atcelts |
28616 | EN ISO 10993-10:2010 | Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO/DIS 10993-10:2008) | Atcelts |
9488 | EN ISO 10993-14:2001 | Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001) | Atcelts |
37236 | EN ISO 14155:2011/AC:2011 | Clinical investigation of medical devices for human subjects - Good clinical practice - Technical Corrigendum 1 (ISO 14155:2011/Cor 1:2011) | Atcelts |
32005 | EN ISO 10993-1:2009 | Biological evaluation of medical devices - Part 1: Evaluation and testing (ISO 10993-1:2003) | Atcelts |
32006 | EN ISO 10993-6:2009 | Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2007) | Atcelts |
23724 | EN ISO 10993-10:2002/A1:2006 | Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity - Amendment 1 (ISO 10993-10:2002/Amd 1:2006) | Atcelts |
Displaying 131-140 of 192 results.