ASTM F2451 Standard Guide for in vivo Assessment of Implantable Devices Intended to Repair or Regenerate Articular Cartilage
Список продуктов
Данный раздел/документ содержится в продуктах:
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 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 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 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 F763 Standard Practice for Short-Term Screening of Implant Materials
- 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 F895 Standard Test Method for Agar Diffusion Cell Culture Screening for Cytotoxicity
- ASTM F2721 Standard Guide for Pre-clinical in vivo Evaluation in Critical Size Segmental Bone Defects
- ASTM F2451 Standard Guide for in vivo Assessment of Implantable Devices Intended to Repair or Regenerate Articular Cartilage
- Картотека зарубежных и международных стандартов
На него ссылаются
- В списке элементов: 3
- DIN ISO 13022 Medical products containing viable human cells - Application of risk management and requirements for processing practices (ISO 13022:2012)Медицинские продукты, которые содержат живущие клетки человеческого происхождения - применение менеджмента риска и требования к практике использования (ИЗО 13022:2012)
Карточка документа - ISO 13022 Medical products containing viable human cells - Application of risk management and requirements for processing practices - First EditionЛекарственные препараты, содержащие жизнеспособные клетки человека - Применение управления рисками и требований для обработки практики - Первый Выпуск
На основе ISO 13022 разработан ГОСТ Р ИСО 13022-2016 (IDT)ГОСТ Р ИСО 13022-2016 (IDT) - ASTM F2721 Standard Guide for Pre-clinical in vivo Evaluation in Critical Size Segmental Bone DefectsТипичный Гид для Преклинического в естественных условиях Оценка в Критическом Размере Сегментальные Дефекты кости
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