CEN/TC 206
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
32007 | LVS EN ISO 10993-11:2009 | Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006) | Atcelts |
9500 | LVS EN ISO 10993-18:2005 | Biological evaluation of medical devices - Part 18: Chemical characterization of materials | Atcelts |
31999 | 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 |
21140 | LVS EN ISO 10993-12:2005 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials | Atcelts |
9495 | LVS EN ISO 10993-3:2003 | Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity | Atcelts |
22598 | LVS EN ISO 10993-1:2003 | Biological evaluation of medical devices - Part 1: Evaluation and testing | Atcelts |
9499 | LVS EN ISO 10993-17:2003 | Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances | Atcelts |
9496 | LVS EN ISO 10993-4:2003 | Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood | Atcelts |
9488 | LVS EN ISO 10993-14:2003 | Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics | 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 |
Displaying 71-80 of 192 results.