Registration number (WIID)Project No.TitleStatus
30398EN ISO 10993-3:2014Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO/DIS 10993-3:2011)Standarts spēkā
77335prEN ISO 18969Clinical evaluation of medical devices (ISO/DIS 18969:2025)Aptauja slēgta
78812prEN ISO 21762Medical devices utilizing non-viable human materials - Risk management (ISO/DIS 21762:2025)Aptauja slēgta
78991prEN ISO 10993-16Biological evaluation of medical devices - Part 16: Toxicokinetic evaluation for degradation products and leachables (ISO/DIS 10993-16:2025)Aptauja slēgta
77933prEN ISO 10993-11Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO/DIS 10993-11:2026)Aptauja
9488EN ISO 10993-14:2001Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001)Atcelts
28616EN ISO 10993-10:2010Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO/DIS 10993-10:2008)Atcelts
37559EN ISO 14155:2011Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011)Atcelts
9499EN ISO 10993-17:2002Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)Atcelts
9489LVS EN ISO 10993-15:2003Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloysAtcelts
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