Registration number (WIID)Project No.TitleStatus
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
78991prEN ISO 10993-16Biological evaluation of medical devices - Part 16: Toxicokinetic evaluation for degradation products and leachables (ISO/DIS 10993-16:2025)Aptauja slēgta
78812prEN ISO 21762Medical devices utilizing non-viable human materials - Risk management (ISO/DIS 21762:2025)Aptauja slēgta
77335prEN ISO 18969Clinical evaluation of medical devices (ISO/DIS 18969:2025)Aptauja slēgta
77933prEN ISO 10993-11Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO/DIS 10993-11:2026)Aptauja
9501LVS EN ISO 10993-10:2003Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivityAtcelts
9471EN 30993-1:1994Biological evaluation of medical devices - Part 1: Guidance on selection of tests (ISO 10993-1:1992 + Technical Corrigendum 1:1992)Atcelts
32001EN ISO 10993-15:2009Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000)Atcelts
9500EN ISO 10993-18:2005Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005)Atcelts
9489EN ISO 10993-15:2000Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000)Atcelts
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