Registration number (WIID)Project No.TitleStatus
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
77391FprEN ISO 10993-6Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO/FDIS 10993-6:2025)Izstrādē
75885FprEN ISO 10993-7Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO/FDIS 10993-7:2025)Izstrādē
77182FprEN ISO 14155Clinical investigation of medical devices for human subjects - Good clinical practice (ISO/FDIS 14155:2025)Izstrādē
9471LVS EN 30993-1:1994Biological evaluation of medical devices - Part 1: Guidance on selection of tests (ISO 10993-1:1992 + Technical Corrigendum 1:1992)Atcelts
9475LVS EN 30993-3:1993Biological evalution of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicityAtcelts
9479LVS EN 30993-4:1993Biological evalution of medical devices - Part 4: Selection of tests for interactions with bloodAtcelts
9472LVS EN 30993-5:1994Biological evaluation of medical devices - Part 5: Tests for cytotoxicity - in vitro methods (ISO 10993-5:1992)Atcelts
9480LVS EN 30993-6:1994Biological evalution of medical devices - Part 6: Tests for local effects after implantationAtcelts
9477LVS EN ISO 10993-10:1995Biological evalution of medical devices - Part 10: Tests for irritation and sensitizationAtcelts
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