Registration number (WIID)Project No.TitleStatus
27092LVS EN ISO 10993-1:2010Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2009)Atcelts
9489LVS EN ISO 10993-15:2003Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloysAtcelts
9475LVS EN 30993-3:1993Biological evalution of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicityAtcelts
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
32007EN ISO 10993-11:2009Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006)Atcelts
9477EN ISO 10993-10:1995Biological evaluation of medical devices - Part 10: Tests for irritation and sensitization (ISO 10993-10:1995)Atcelts
9488EN ISO 10993-14:2001Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001)Atcelts
37236EN ISO 14155:2011/AC:2011Clinical investigation of medical devices for human subjects - Good clinical practice - Technical Corrigendum 1 (ISO 14155:2011/Cor 1:2011)Atcelts
32005EN ISO 10993-1:2009Biological evaluation of medical devices - Part 1: Evaluation and testing (ISO 10993-1:2003)Atcelts
32006EN ISO 10993-6:2009Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2007)Atcelts
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