Registration number (WIID)Project No.TitleStatus
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 process (ISO 10993-1:2009)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
9477EN ISO 10993-10:1995Biological evaluation of medical devices - Part 10: Tests for irritation and sensitization (ISO 10993-10:1995)Atcelts
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
9497EN ISO 10993-5:1999Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:1999)Atcelts
9472EN 30993-5:1994Biological evaluation of medical devices - Part 5: Tests for cytotoxicity - in vitro methods (ISO 10993-5:1992)Atcelts
9499EN ISO 10993-17:2002Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)Atcelts
9496EN ISO 10993-4:2002Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2002)Atcelts
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