Registration number (WIID)Project No.TitleStatus
35184LVS EN ISO 10993-1:2010 /AC:2010Biological 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
24852LVS EN ISO 10993-12:2008Biological evaluation of medical devices - Part 12: Sample preparation and reference materialsAtcelts
27050LVS EN ISO 10993-9:2010Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:2009)Atcelts
9496LVS EN ISO 10993-4:2003Biological evaluation of medical devices - Part 4: Selection of tests for interactions with bloodAtcelts
37236EN ISO 14155:2011/AC:2011Clinical investigation of medical devices for human subjects - Good clinical practice - Technical Corrigendum 1 (ISO 14155:2011/Cor 1:2011)Atcelts
32005EN ISO 10993-1:2009Biological evaluation of medical devices - Part 1: Evaluation and testing (ISO 10993-1:2003)Atcelts
9500EN ISO 10993-18:2005Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005)Atcelts
22132LVS EN ISO 10993-2:2006Biological evaluation of medical devices - Part 2: Animal welfare requirementsAtcelts
32003LVS EN ISO 10993-17:2009Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)Atcelts
40624LVS EN ISO 10993-10:2013Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO 10993-10:2010)Atcelts
Displaying 101-110 of 194 results.