Biological Evaluation of Medical Devices - Part 13: Identification and Quantification of Degradation Products From Polymeric Medical Devices (Adopted ISO 10993-13:1998, first edition, 1998-11-15)
Document status: [ Withdrawn ]
Biological Evaluation of Medical Devices - Part 16: Toxicokinetic Study Design for Degradation Products and Leachables (Adopted ISO 10993-16:1997, first edition, 1997-09-01)
Document status: [ Withdrawn ]
Biological Evaluation of Medical Devices - Part 2: Animal Welfare Requirements (Adopted ISO 10993-2:1992)
Document status: [ Withdrawn ]
Biological Evaluation of Medical Devices - Part 3: Tests for Genotoxicity, Carcinogenicity and Reproductive Toxicity (Adopted ISO 10993-3:1992)
Document status: [ Withdrawn ]
Biological Evaluation of Medical Devices - Part 4: Selection of Tests for Interactions With Blood (Adopted ISO 10993-4:1992)
Document status: [ Withdrawn ]
Biological evaluation of medical devices- Part 5: Tests for in vitro cytotoxicity
Document status: [ Withdrawn ]
Biological Evaluation of Medical Devices - Part 6: Tests for Local Effects After Implantation (Adopted ISO 10993-6:1994)
Document status: [ Withdrawn ]
Biological Evaluation of Medical Devices - Part 7: Ethylene Oxide Sterilization Residuals (Adopted ISO 10993-7:1995)
Document status: [ Withdrawn ]
Biological Evaluation of Medical Devices - Part 9: Framework for Identification and Quantification of Potential Degradation Products (Adopted ISO 10993-9:1999, first edition, 1999-03-01)
Document status: [ Withdrawn ]
Sterilization of Health Care Products - Requirements for Validation and Routine Control - Industrial Moist Heat Sterilization (Adopted ISO 11134:1994)
Document status: Active
