Registration number (WIID)Project No.TitleStatus
27092LVS EN ISO 10993-1:2010Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2009)Atcelts
31981LVS EN ISO 10993-9:2009Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:1999)Atcelts
21140LVS EN ISO 10993-12:2005Biological evaluation of medical devices - Part 12: Sample preparation and reference materialsAtcelts
40815LVS EN ISO 10993-4:2017Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017)Atcelts
31979LVS EN ISO 10993-4:2009Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2002, including Amd 1:2006)Atcelts
32001LVS EN ISO 10993-15:2009Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000)Atcelts
24852LVS EN ISO 10993-12:2008Biological evaluation of medical devices - Part 12: Sample preparation and reference materialsAtcelts
24852EN ISO 10993-12:2007Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2007)Atcelts
40624LVS EN ISO 10993-10:2013Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO 10993-10:2010)Atcelts
32008LVS EN ISO 10993-12:2009Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2007)Atcelts
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