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
75596LVS EN ISO 10993-1:2025Biological evaluation of medical devices - Part 1: Requirements and general principles for the evaluation of biological safety within a risk management process (ISO 10993-1:2025)Standarts spēkā
78994LVS EN ISO 10993-17:2023/A1:2025Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents - Amendment 1 (ISO 10993-17:2023/Amd 1:2025)Standarts spēkā
77182EN ISO 14155:2026Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2026)Standarts spēkā
77182LVS EN ISO 14155:2026Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2026)Standarts spēkā
75885LVS EN ISO 10993-7:2026Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2026)Standarts spēkā
65480EN ISO 22442-1:2020Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management (ISO 22442-1:2020)Standarts spēkā
27051LVS EN ISO 10993-13:2010Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:2010)Standarts spēkā
38319LVS EN ISO 10993-6:2017Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2016)Standarts spēkā
77391LVS EN ISO 10993-6:2026Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2026) 
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