ASTM F2212 Standard Guide for Characterization of Type I Collagen as Starting Material for Surgical Implants and Substrates for Tissue Engineered Medical Products (TEMPs)
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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
- 13
- 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 22442-2 Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling - Second EditionМедицинские устройства, использующие ткани животных и их производные - Часть 2: Контроль над сорсингом, коллекцией и обработкой - Второй Выпуск
Карточка документа - ISO 22442-1 Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management - Second EditionМедицинские устройства, использующие ткани животных и их производные - Часть 1: Применение управления рисками - Второй Выпуск
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 10993-3 Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity - Third EditionБиологическая оценка медицинских устройств - Часть 3: Анализы на генотоксичность, онкогенность и репродуктивную токсичность - Третий Выпуск
Карточка документа - ASTM F1904 Standard Practice for Testing the Biological Responses to Particles in vivoОбщепринятая практика для Тестирования Биологических реакций к Частицам в естественных условиях
Карточка документа - ASTM F619 Standard Practice for Extraction of Medical PlasticsОбщепринятая практика для извлечения медицинской пластики
Карточка документа - ASTM F756 Standard Practice for Assessment of Hemolytic Properties of MaterialsОбщепринятая практика для оценки гемолитических свойств материалов
Карточка документа - ASTM F720 Standard Practice for Testing Guinea Pigs for Contact Allergens: Guinea Pig Maximization TestОбщепринятая практика для тестирования морских свинок для аллергенов контакта: анализ максимизации морской свинки
Карточка документа - ASTM F2148 Standard Practice for Evaluation of Delayed Contact Hypersensitivity Using the Murine Local Lymph Node Assay (LLNA)Общепринятая практика для оценки задержанной аллергии контакта Используя мышиную Пробу регионального лимфатического узла (LLNA)
Карточка документа - ISO 13408-1 AMD 1 Aseptic processing of health care products - Part 1: General requirements AMENDMENT 1 - Second EditionАсептическая обработка продуктов здравоохранения - Часть 1: Общие требования AMENDMENT 1 - Второй Выпуск
Карточка документа - ASTM F749 Standard Practice for Evaluating Material Extracts by Intracutaneous Injection in the RabbitОбщепринятая практика для оценки материальных экстрактов внутрикожной инжекцией у кролика
Карточка документа - ASTM F895 Standard Test Method for Agar Diffusion Cell Culture Screening for CytotoxicityМетод стандартной пробы для агарового показа культуры диффузора на цитотоксичность
Карточка документа - ISO 10993-10 Biological evaluation of medical devices — Part 10: Tests for irritation and skin sensitization - Third EditionБиологическая оценка медицинских устройств — Часть 10: Анализы на раздражение и сенсибилизацию кожи - Третий Выпуск
Карточка документа - 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 - ASTM F1903 Standard Practice for Testing For Biological Responses to Particles In VitroОбщепринятая практика для тестирования на биологические ответы на частицы в пробирке
Карточка документа - 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 22442-3 Medical devices utilizing animal tissues and their derivatives — Part 3: Validation of the elimination and/or inactivation of viruses and transmissible spongiform encephalopathy (TSE) agents - First EditionМедицинские устройства, использующие ткани животных и их производные — Часть 3: Проверка устранения и/или деактивации вирусов и агентов передающейся губкообразной энцефалопатии (TSE) - Первый Выпуск
На основе ISO 22442-3 разработан ГОСТ Р ИСО 22442-3-2011 (IDT)ГОСТ Р ИСО 22442-3-2011 (IDT) - ISO 14971 Medical devices — Application of risk management to medical devices - Second edition; Corrected Version 10/01/2007Медицинские устройства — Применение управления рисками к медицинским устройствам - Второй выпуск; Исправленная Версия 10/01/2007
На основе ISO 14971 разработаны ГОСТ Р ИСО 14971-2009 (IDT); ГОСТ ISO 14971-2011 (IDT)ГОСТ ISO 14971-2011 (IDT) - ASTM F813 Standard Practice for Direct Contact Cell Culture Evaluation of Materials for Medical DevicesОбщепринятая практика для оценки клеточной культуры прямого контакта материалов для медицинских устройств
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 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 - ASTM F1439 Standard Guide for Performance of Lifetime Bioassay for the Tumorigenic Potential of Implant MaterialsТипичный гид для производительности пожизненной биопробы для потенциала Tumorigenic материалов внедрения
Карточка документа - ISO 10993-17 Biological Evaluation of Medical Devices - Part 17: Establishment of Allowable Limits for Leachable Substances - First EditionБиологическая оценка медицинских устройств - часть 17: учреждение допустимых пределов для веществ Leachable - первый выпуск
На основе ISO 10993-17 разработаны ГОСТ Р ИСО 10993-17-2009 (IDT); ГОСТ ISO 10993-17-2011 (IDT)ГОСТ ISO 10993-17-2011 (IDT)
