ISO 10993-6 Biological evaluation of medical devices - Part 6: Tests for local effects after implantation - Third Edition
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Данный раздел/документ содержится в продуктах:
- Техэксперт: Машиностроительный комплекс
- Картотека зарубежных и международных стандартов
- ASTM F2451 Standard Guide for in vivo Assessment of Implantable Devices Intended to Repair or Regenerate Articular Cartilage
- ASTM G125 Standard Test Method for Measuring Liquid and Solid Material Fire Limits in Gaseous Oxidants
- ASTM D618 Standard Practice for Conditioning Plastics for Testing
- ASTM D6712 Standard Specification for Ultra-High-Molecular-Weight Polyethylene (UHMW-PE) Solid Plastic Shapes
- ASTM D4020 Standard Specification for Ultra-High-Molecular-Weight Polyethylene Molding and Extrusion Materials
- ASTM F2695 Standard Specification for Ultra-High Molecular Weight Polyethylene Powder Blended With Alpha-Tocopherol (Vitamin E) and Fabricated Forms for Surgical Implant Applications
- ASTM F981 Standard Practice for Assessment of Compatibility of Biomaterials for Surgical Implants with Respect to Effect of Materials on Muscle and Bone
- ASTM F2721 Standard Guide for Pre-clinical in vivo Evaluation in Critical Size Segmental Bone Defects
- ASTM F981 Standard Practice for Assessment of Compatibility of Biomaterials for Surgical Implants with Respect to Effect of Materials on Muscle and Bone
- ASTM F2695 Standard Specification for Ultra-High Molecular Weight Polyethylene Powder Blended With Alpha-Tocopherol (Vitamin E) and Fabricated Forms for Surgical Implant Applications
- ASTM D4020 Standard Specification for Ultra-High-Molecular-Weight Polyethylene Molding and Extrusion Materials
- ASTM D6712 Standard Specification for Ultra-High-Molecular-Weight Polyethylene (UHMW-PE) Solid Plastic Shapes
- ASTM D618 Standard Practice for Conditioning Plastics for Testing
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- ASTM G125 Standard Test Method for Measuring Liquid and Solid Material Fire Limits in Gaseous Oxidants
- ASTM D618 Standard Practice for Conditioning Plastics for Testing
- ASTM D6712 Standard Specification for Ultra-High-Molecular-Weight Polyethylene (UHMW-PE) Solid Plastic Shapes
- ASTM D4020 Standard Specification for Ultra-High-Molecular-Weight Polyethylene Molding and Extrusion Materials
- ASTM F2695 Standard Specification for Ultra-High Molecular Weight Polyethylene Powder Blended With Alpha-Tocopherol (Vitamin E) and Fabricated Forms for Surgical Implant Applications
- ASTM F981 Standard Practice for Assessment of Compatibility of Biomaterials for Surgical Implants with Respect to Effect of Materials on Muscle and Bone
- ASTM F2721 Standard Guide for Pre-clinical in vivo Evaluation in Critical Size Segmental Bone Defects
- ASTM F981 Standard Practice for Assessment of Compatibility of Biomaterials for Surgical Implants with Respect to Effect of Materials on Muscle and Bone
- ASTM F2695 Standard Specification for Ultra-High Molecular Weight Polyethylene Powder Blended With Alpha-Tocopherol (Vitamin E) and Fabricated Forms for Surgical Implant Applications
- ASTM D4020 Standard Specification for Ultra-High-Molecular-Weight Polyethylene Molding and Extrusion Materials
- ASTM D6712 Standard Specification for Ultra-High-Molecular-Weight Polyethylene (UHMW-PE) Solid Plastic Shapes
- ASTM D618 Standard Practice for Conditioning Plastics for Testing
- 13.220
- ASTM G125 Standard Test Method for Measuring Liquid and Solid Material Fire Limits in Gaseous Oxidants
- ASTM D618 Standard Practice for Conditioning Plastics for Testing
- ASTM D6712 Standard Specification for Ultra-High-Molecular-Weight Polyethylene (UHMW-PE) Solid Plastic Shapes
- ASTM D4020 Standard Specification for Ultra-High-Molecular-Weight Polyethylene Molding and Extrusion Materials
- ASTM F2695 Standard Specification for Ultra-High Molecular Weight Polyethylene Powder Blended With Alpha-Tocopherol (Vitamin E) and Fabricated Forms for Surgical Implant Applications
- ASTM F981 Standard Practice for Assessment of Compatibility of Biomaterials for Surgical Implants with Respect to Effect of Materials on Muscle and Bone
- ASTM F2721 Standard Guide for Pre-clinical in vivo Evaluation in Critical Size Segmental Bone Defects
- ASTM F981 Standard Practice for Assessment of Compatibility of Biomaterials for Surgical Implants with Respect to Effect of Materials on Muscle and Bone
- ASTM F2695 Standard Specification for Ultra-High Molecular Weight Polyethylene Powder Blended With Alpha-Tocopherol (Vitamin E) and Fabricated Forms for Surgical Implant Applications
- ASTM D4020 Standard Specification for Ultra-High-Molecular-Weight Polyethylene Molding and Extrusion Materials
- ASTM D6712 Standard Specification for Ultra-High-Molecular-Weight Polyethylene (UHMW-PE) Solid Plastic Shapes
- ASTM D618 Standard Practice for Conditioning Plastics for Testing
- ASTM G125 Standard Test Method for Measuring Liquid and Solid Material Fire Limits in Gaseous Oxidants
- ASTM G125 Standard Test Method for Measuring Liquid and Solid Material Fire Limits in Gaseous Oxidants
- ASTM D6712 Standard Specification for Ultra-High-Molecular-Weight Polyethylene (UHMW-PE) Solid Plastic Shapes
- ASTM D4020 Standard Specification for Ultra-High-Molecular-Weight Polyethylene Molding and Extrusion Materials
- ASTM F2695 Standard Specification for Ultra-High Molecular Weight Polyethylene Powder Blended With Alpha-Tocopherol (Vitamin E) and Fabricated Forms for Surgical Implant Applications
- ASTM F981 Standard Practice for Assessment of Compatibility of Biomaterials for Surgical Implants with Respect to Effect of Materials on Muscle and Bone
- ASTM F2721 Standard Guide for Pre-clinical in vivo Evaluation in Critical Size Segmental Bone Defects
- ASTM F981 Standard Practice for Assessment of Compatibility of Biomaterials for Surgical Implants with Respect to Effect of Materials on Muscle and Bone
- ASTM F2695 Standard Specification for Ultra-High Molecular Weight Polyethylene Powder Blended With Alpha-Tocopherol (Vitamin E) and Fabricated Forms for Surgical Implant Applications
- ASTM D4020 Standard Specification for Ultra-High-Molecular-Weight Polyethylene Molding and Extrusion Materials
- ASTM D4020 Standard Specification for Ultra-High-Molecular-Weight Polyethylene Molding and Extrusion Materials
- ASTM F2695 Standard Specification for Ultra-High Molecular Weight Polyethylene Powder Blended With Alpha-Tocopherol (Vitamin E) and Fabricated Forms for Surgical Implant Applications
- ASTM F981 Standard Practice for Assessment of Compatibility of Biomaterials for Surgical Implants with Respect to Effect of Materials on Muscle and Bone
- ASTM F2721 Standard Guide for Pre-clinical in vivo Evaluation in Critical Size Segmental Bone Defects
- ASTM F981 Standard Practice for Assessment of Compatibility of Biomaterials for Surgical Implants with Respect to Effect of Materials on Muscle and Bone
- ASTM F2695 Standard Specification for Ultra-High Molecular Weight Polyethylene Powder Blended With Alpha-Tocopherol (Vitamin E) and Fabricated Forms for Surgical Implant Applications
- ASTM F2695 Standard Specification for Ultra-High Molecular Weight Polyethylene Powder Blended With Alpha-Tocopherol (Vitamin E) and Fabricated Forms for Surgical Implant Applications
- ASTM F981 Standard Practice for Assessment of Compatibility of Biomaterials for Surgical Implants with Respect to Effect of Materials on Muscle and Bone
- ASTM F2721 Standard Guide for Pre-clinical in vivo Evaluation in Critical Size Segmental Bone Defects
- ASTM F981 Standard Practice for Assessment of Compatibility of Biomaterials for Surgical Implants with Respect to Effect of Materials on Muscle and Bone
- ASTM F981 Standard Practice for Assessment of Compatibility of Biomaterials for Surgical Implants with Respect to Effect of Materials on Muscle and Bone
- ASTM F2721 Standard Guide for Pre-clinical in vivo Evaluation in Critical Size Segmental Bone Defects
- ASTM F2721 Standard Guide for Pre-clinical in vivo Evaluation in Critical Size Segmental Bone Defects
- ASTM F895 Standard Test Method for Agar Diffusion Cell Culture Screening for Cytotoxicity
- ASTM F2212 Standard Guide for Characterization of Type I Collagen as Starting Material for Surgical Implants and Substrates for Tissue Engineered Medical Products (TEMPs)
- ASTM F763 Standard Practice for Short-Term Screening of Implant Materials
- Картотека зарубежных и международных стандартов
Ссылается на
- В списке элементов: 24
- ISO 5832-7 Implants for surgery - Metallic materials - Part 7: Forgeable and cold-formed cobaltchromium- nickel-molybdenum-iron alloyИмплантаты для хирургии - Металлические материалы - Часть 7: Ковкий и сформированный простудой cobaltchromium-сплав железа молибдена никеля
Карточка документа - ISO 5832-3 Implants for surgery - Metallic materials - Part 3: Wrought titanium 6-aluminium 4-vanadium alloy - Fourth EditionИмплантаты для хирургии - Металлические материалы - Часть 3: Выделанный титан сплав с 4 ванадиями с 6 алюминиями - Четвертый Выпуск
Карточка документа - ISO 5832-1 Implants for surgery - Metallic materials - Part 1: Wrought stainless steel - Fifth EditionИмплантаты для хирургии - Металлические материалы - Часть 1: Выделанная нержавеющая сталь - Пятый Выпуск
Карточка документа - ASTM F748 Standard Practice for Selecting Generic Biological Test Methods for Materials and DevicesУтвержденный технологический процесс для отбора универсальных методов биологического теста для материалов и устройств
Карточка документа - ASTM F1983 Standard Practice for Assessment of Selected Tissue Effects of Absorbable Biomaterials for Implant ApplicationsОбщепринятая практика для оценки отобранных эффектов ткани поглощаемых биоматериалов для приложений имплантата
Карточка документа - ISO 5832-4 Implants for surgery - Metallic materials - Part 4: Cobalt-chromium-molybdenum casting alloy - Third EditionИмплантаты для хирургии - Металлические материалы - Часть 4: литейный сплав молибдена хрома кобальта - Третий Выпуск
Карточка документа - ISO 7405 AMD 1 Dentistry - Evaluation of biocompatibility of medical devices used in dentistry AMENDMENT 1: Positive control material - Second EditionСтоматология - Оценка биологической совместимости медицинских устройств использовала в стоматологии AMENDMENT 1: материал Надежного управления - Второй Выпуск
Карточка документа - ISO 10993-12 Biological evaluation of medical devices - Part 12: Sample preparation and reference materials - Fourth EditionБиологическая оценка медицинских устройств - Часть 12: Подготовка пробы и справочные материалы - Четвертый Выпуск
На основе ISO 10993-12 разработан ГОСТ ISO 10993-12-2015 (IDT)ГОСТ ISO 10993-12-2015 (IDT) - ISO 6474-2 Implants for surgery - Ceramic materials - Part 2: Composite materials based on a highpurity alumina matrix with zirconia reinforcement - First EditionИмплантаты для хирургии - Керамические материалы - Часть 2: Композиционные материалы на основе highpurity матрицы глинозема с укреплением двуокиси циркония - Первый Выпуск
На основе ISO 6474-2 разработан ГОСТ Р ИСО 6474-2-2014 (IDT)ГОСТ Р ИСО 6474-2-2014 (IDT) - ISO 5834-2 Implants for surgery — Ultra-high-molecular-weight polyethylene — Part 2: Moulded forms - Fourth EditionИмплантаты для хирургии — Крайнего полиэтилена высокого молекулярного веса — Часть 2: Формируемые формы - Четвертый Выпуск
На основе ISO 5834-2 разработан ГОСТ Р ИСО 5834-2-2014 (IDT)ГОСТ Р ИСО 5834-2-2014 (IDT) - ISO 10993-1 CORR 1 Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management process TECHNICAL CORRIGENDUM 1 - Fourth EditionБиологическая оценка медицинских устройств — Часть 1: Оценка и проверяющий в управлении рисками обрабатывает TECHNICAL CORRIGENDUM 1 - Четвертый Выпуск
Карточка документа - ISO 6474-1 Implants for surgery — Ceramic materials — Part 1: Ceramic materials based on high purity alumina - First EditionИмплантаты для хирургии — Керамические материалы — Часть 1: Керамические материалы на основе высокочистого глинозема - Первый Выпуск
На основе ISO 6474-1 разработан ГОСТ Р ИСО 6474-1-2014 (IDT)ГОСТ Р ИСО 6474-1-2014 (IDT) - ISO 10993-16 Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachables - Second EditionБиологическая оценка медицинских устройств — Часть 16: Toxicokinetic изучают дизайн для продуктов ухудшения и leachables - Второй Выпуск
На основе ISO 10993-16 разработан ГОСТ ISO 10993-16-2016 (IDT)ГОСТ ISO 10993-16-2016 (IDT) - ISO 10993-9 Biological evaluation of medical devices — Part 9: Framework for identification and quantification of potential degradation products - Second EditionБиологическая оценка медицинских устройств — Часть 9: Зубной мост для идентификации и определения количества потенциальных продуктов ухудшения - Второй Выпуск
На основе ISO 10993-9 разработан ГОСТ ISO 10993-9-2015 (IDT)ГОСТ ISO 10993-9-2015 (IDT) - ISO 10993-11 Biological evaluation of medical devices Part 11: Tests for systemic toxicity - Second EditionБиологическая оценка Части 11 медицинских устройств: Анализы на системную токсичность - Второй Выпуск
На основе ISO 10993-11 разработаны ГОСТ Р ИСО 10993-11-2009 (IDT); ГОСТ ISO 10993-11-2011 (IDT)ГОСТ ISO 10993-11-2011 (IDT) - ISO 10993-2 Biological evaluation of medical devices Part 2: Animal welfare requirements - Second EditionБиологическая оценка Части 2 медицинских устройств: требования Защиты животных - Второй Выпуск
На основе ISO 10993-2 разработан ГОСТ Р ИСО 10993-2-2009 (IDT)ГОСТ Р ИСО 10993-2-2009 (IDT) - ISO 10993-4 AMD 1 Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood AMENDMENT 1 - Second EditionБиологическая оценка медицинских приборов — Часть 4. исследование изделий, взаимодействующих с поправкой крови 1 - второе издание
Карточка документа - ISO 11979-5 Ophthalmic Implants - Intraocular Lenses - Part 5: Biocompatibility - Second EditionГлазные имплантаты - внутриглазные хрусталики - часть 5: биологическая совместимость - второй выпуск
На основе ISO 11979-5 разработан ГОСТ Р 52858-2007 (MOD)ГОСТ Р 52858-2007 (MOD) - ISO 5832-5 Implants for surgery Metallic materials Part 5: Wrought cobalt-chromium-tungsten-nickel alloy - Third EditionИмплантаты для хирургии Металлическая Часть 5 материалов: Выделанный сплав никеля вольфрама хрома кобальта - Третий Выпуск
На основе ISO 5832-5 разработан ГОСТ Р ИСО 5832-5-2010 (IDT)ГОСТ Р ИСО 5832-5-2010 (IDT) - ASTM F981 Standard Practice for Assessment of Compatibility of Biomaterials for Surgical Implants with Respect to Effect of Materials on Muscle and BoneУтвержденный технологический процесс для оценки совместимости биоматериалов для хирургических внедрений относительно результата материалов на мышце и кости
Карточка документа - ASTM F763 Standard Practice for Short-Term Screening of Implant MaterialsУтвержденный технологический процесс для краткосрочного показа материалов внедрения
Карточка документа - ISO 5832-2 Implants for Surgery - Metallic Materials - Part 2: Unalloyed Titanium - Third EditionИмплантаты для хирургии - металлические материалы - часть 2: чистый титан - третий выпуск
На основе ISO 5832-2 разработан ГОСТ Р ИСО 5832-2-2014 (IDT)ГОСТ Р ИСО 5832-2-2014 (IDT) - ISO 5832-8 Implants for Surgery - Metallic Materials - Part 8: Wrought Cobalt-Nickel-Chromium-Molybdenum-Tungsten-Iron Alloy - Second EditionИмплантаты для хирургии - металлические материалы - часть 8: вызванный Cobalt-Nickel-Chromium-Molybdenum-Tungsten-Iron сплав - второй выпуск
На основе ISO 5832-8 разработаны ГОСТ Р ИСО 5832-8-2010 (IDT); ГОСТ 31624-2012 (NEQ)ГОСТ 31624-2012 (NEQ) - ISO 5832-6 Implants for Surgery - Metallic Materials - Part 6: Wrought Cobalt-Nickel-Chromium-Molybdenum Alloy - Second EditionИмплантаты для хирургии - металлические материалы - часть 6: выделанный сплав молибдена хрома никеля кобальта - второй выпуск
На основе ISO 5832-6 разработаны ГОСТ Р 51396-99 (NEQ); ГОСТ Р ИСО 5832-6-2010 (IDT); ГОСТ 31624-2012 (NEQ)ГОСТ 31624-2012 (NEQ)
