Registration number (WIID)Project No.TitleStatus
75596EN 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
25795EN ISO 22442-3:2007Medical devices utilizing animal tissues and their derivatives - Part 3: Validation of the elimination and/or inactivation of viruses and transmissible spongiform encephalopathy (TSE) agents (ISO 22442-3:2007)Standarts spēkā
65727EN ISO 10993-4:2017Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017)Standarts spēkā
65481EN ISO 22442-2:2020Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO 22442-2:2020)Standarts spēkā
77391EN ISO 10993-6:2026Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2026)Standarts spēkā
77182LVS EN ISO 14155:2026Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2026) 
77391LVS EN ISO 10993-6:2026Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2026) 
75885LVS EN ISO 10993-7:2026Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2026) 
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