Registration number (WIID)Project No.TitleStatus
32006LVS EN ISO 10993-6:2009Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2007)Atcelts
9478LVS EN ISO 10993-11:1995Biological evalution of medical devices - Part 11: Tests for systemic toxicityAtcelts
9493LVS EN ISO 10993-7:2009Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008)Atcelts
31999EN ISO 10993-13:2009Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:1998)Atcelts
28616LVS EN ISO 10993-10:2011Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO 10993-10:2010)Atcelts
60214EN ISO 22442-2:2015Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO/FDIS 22442-2:2015)Atcelts
9499LVS EN ISO 10993-17:2003Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substancesAtcelts
9489EN ISO 10993-15:2000Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000)Atcelts
40815LVS EN ISO 10993-4:2017Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017)Atcelts
79539LVS EN ISO 14155:2020/A11:2024Clinical investigation of medical devices for human subjects - Good clinical practiceAtcelts
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