Registration number (WIID)Project No.TitleStatus
31982EN ISO 10993-10:2009Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity (ISO 10993-10:2002, including Amd 1:2006)Atcelts
22598EN ISO 10993-1:2003Biological evaluation of medical devices - Part 1: Evaluation and testing (ISO 10993-1:2003)Atcelts
32007EN ISO 10993-11:2009Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006)Atcelts
32002EN ISO 10993-16:2009Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:1997)Atcelts
22132LVS EN ISO 10993-2:2006Biological evaluation of medical devices - Part 2: Animal welfare requirementsAtcelts
30062EN ISO 10993-16:2010Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO/DIS 10993-16:2008)Atcelts
9496EN ISO 10993-4:2002Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2002)Atcelts
9494EN ISO 10993-16:1997Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:1997)Atcelts
9488EN ISO 10993-14:2001Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001)Atcelts
40815EN ISO 10993-4:2017Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017)Atcelts
Displaying 81-90 of 190 results.