Registration number (WIID)Project No.TitleStatus
44049ISO 10993-9:2009Biological evaluation of medical devices — Part 9: Framework for identification and quantification of potential degradation productsAtcelts
26211ISO 10993-5:1999Biological evaluation of medical devices — Part 5: Tests for in vitro cytotoxicityAtcelts
44789ISO 10993-6:2007Biological evaluation of medical devices — Part 6: Tests for local effects after implantationAtcelts
36403ISO/TS 20993:2006Biological evaluation of medical devices — Guidance on a risk-management processAtcelts
55064ISO 10993-7:2008/Cor 1:2009Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals — Technical Corrigendum 1Atcelts
41106ISO 10993-18:2005Biological evaluation of medical devices — Part 18: Chemical characterization of materialsAtcelts
53468ISO 10993-12:2012Biological evaluation of medical devices — Part 12: Sample preparation and reference materialsAtcelts
18971ISO 10993-10:1995Biological evaluation of medical devices — Part 10: Tests for irritation and sensitizationAtcelts
56669ISO 10993-1:2009/Cor 1:2010Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management process — Technical Corrigendum 1Atcelts
35977ISO 10993-11:2006Biological evaluation of medical devices — Part 11: Tests for systemic toxicityAtcelts
Displaying 71-80 of 156 results.