Registration number (WIID)Project No.TitleStatus
77933prEN ISO 10993-11Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO/DIS 10993-11:2025)Aptauja slēgta
78812prEN ISO 21762Medical devices utilizing non-viable human materials - Risk management (ISO/DIS 21762:2025)Aptauja
9481EN ISO 10993-7:1995Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:1995)Atcelts
9480EN 30993-6:1994Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:1994)Atcelts
9477EN ISO 10993-10:1995Biological evaluation of medical devices - Part 10: Tests for irritation and sensitization (ISO 10993-10:1995)Atcelts
32002LVS EN ISO 10993-16:2009Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:1997)Atcelts
32007EN ISO 10993-11:2009Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006)Atcelts
27092EN ISO 10993-1:2009Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management system (ISO/FDIS 10993-1:2009)Atcelts
32003LVS EN ISO 10993-17:2009Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)Atcelts
9475LVS EN 30993-3:1993Biological evalution of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicityAtcelts
Displaying 61-70 of 192 results.