DIN EN ISO 10993-6:2009-08
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BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 6: TESTS FOR LOCAL EFFECTS AFTER IMPLANTATION (ISO 10993-6:2016) |
ISO 10993-3:2014
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Biological evaluation of medical devices — Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity |
ISO 10993-16:2017
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Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachables |
DIN EN ISO 10993-2:2006-10
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Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:2006) |
ISO 10993-13:2010
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Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devices |
DIN ISO 6344-1:2000-04
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Coated abrasives - Grain size analysis - Part 1: Grain size distribution test (ISO 6344-1:1999) |
DIN EN ISO 10993-11:2015-12 (Draft)
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BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 11: TESTS FOR SYSTEMIC TOXICITY |
DIN EN ISO 14971:2013-04
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MEDICAL DEVICES - APPLICATION OF RISK MANAGEMENT TO MEDICAL DEVICES (ISO 14971:2007) |
ISO 10993-2:2006
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Biological evaluation of medical devices — Part 2: Animal welfare requirements |
ISO 10993-14:2001
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Biological evaluation of medical devices — Part 14: Identification and quantification of degradation products from ceramics |
ISO 10993-18:2005
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Biological evaluation of medical devices Part 18: Chemical characterization of materials |
DIN EN ISO 10993-5:2009-10
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BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 5: TESTS FOR IN VITRO CYTOTOXICITY |
ISO 10993-10:2010
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Biological evaluation of medical devices Part 10: Tests for irritation and skin sensitization |
ISO 1942:2009
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Dentistry Vocabulary |
ISO 10993-11:2017
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Biological evaluation of medical devices — Part 11: Tests for systemic toxicity |
DIN EN ISO 10993-12:2012-10
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Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012) |
ISO 10993-12:2012
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Biological evaluation of medical devices Part 12: Sample preparation and reference materials |
ISO 10993-7:2008
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Biological evaluation of medical devices Part 7: Ethylene oxide sterilization residuals |
ISO 10993-17:2002
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Biological evaluation of medical devices — Part 17: Establishment of allowable limits for leachable substances |
ADA 41 : 2015
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EVALUATION OF BIOCOMPATIBILITY OF MEDICAL DEVICES USED IN DENTISTRY |
ISO 10993-1:2009
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Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process |
DIN EN ISO 10993-10:2014-10
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Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO 10993-10:2010) |
ISO 10993-9:2009
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Biological evaluation of medical devices Part 9: Framework for identification and quantification of potential degradation products |
ISO 6344-1:1998
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Coated abrasives Grain size analysis Part 1: Grain size distribution test |
DIN EN ISO 1942:2011-03
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Dentistry - Vocabulary (ISO 1942:2009, Corrected version 2010-03-01) |
ISO 14971:2007
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Medical devices Application of risk management to medical devices |
ISO 10993-6:2016
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Biological evaluation of medical devices Part 6: Tests for local effects after implantation |
DIN EN ISO 10993-9:2010-04
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Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:2009) |
DIN EN ISO 10993-3:2015-02
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BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 3: TESTS FOR GENOTOXICITY, CARCINOGENICITY AND REPRODUCTIVE TOXICITY (ISO 10993-3:2014) |
ISO/TS 22911:2016
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Dentistry Preclinical evaluation of dental implant systems Animal test methods |