Registration number (WIID)Project No.TitleStatus
9486EN ISO 10993-12:1996Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:1996)Atcelts
21140EN ISO 10993-12:2004Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2002)Atcelts
9478EN ISO 10993-11:1995Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:1993)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
9479EN 30993-4:1993Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:1992)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
37559EN ISO 14155:2011Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011)Atcelts
40815EN ISO 10993-4:2017Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO/DIS 10993-4:2015)Atcelts
22598EN ISO 10993-1:2003Biological evaluation of medical devices - Part 1: Evaluation and testing (ISO 10993-1:2003)Atcelts
64034EN ISO 10993-7:2008/A1:2022Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals - Amendment 1: Applicability of allowable limits for neonates and infants (ISO 10993-7:2008/Amd 1:2019)Atcelts
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