Registration number (WIID)Project No.TitleStatus
60133LVS EN ISO 10993-11:2018Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2017)Standarts spēkā
62983LVS EN ISO 14155:2020Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)Standarts spēkā
9493LVS EN ISO 10993-7:2009Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008)Standarts spēkā
32000LVS EN ISO 10993-14:2009Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001)Standarts spēkā
60725LVS EN ISO 10993-18:2020Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020)Standarts spēkā
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
67767LVS EN ISO 10993-17:2023Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023)Standarts spēkā
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
78989EN ISO 10993-12:2021/A1:2025Biological evaluation of medical devices - Part 12: Sample preparation and reference materials - Amendment 1 (ISO 10993 12:2021/Amd 1:2025)Standarts spēkā
67187LVS EN ISO 10993-10:2023Biological evaluation of medical devices - Part 10: Tests for skin sensitization (ISO 10993-10:2021)Standarts spēkā
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