Registration number (WIID)Project No.TitleStatus
75885LVS EN ISO 10993-7:2026Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2026) 
9498LVS EN ISO 10993-8:2001Biological evaluation of medical devices - Part 8: Selection and qualification of reference materials for biological testsAtcelts
9482LVS EN ISO 10993-9:2000Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation productsAtcelts
31981LVS EN ISO 10993-9:2009Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:1999)Atcelts
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
60722LVS EN ISO 10993-9:2021Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:2019)Standarts spēkā
62983LVS EN ISO 14155:2020Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)Standarts spēkā
79539LVS EN ISO 14155:2020/A11:2024Clinical investigation of medical devices for human subjects - Good clinical practiceStandarts spēkā
77182LVS EN ISO 14155:2026Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2026) 
65480LVS EN ISO 22442-1:2021Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management (ISO 22442-1:2020)Standarts spēkā
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