BSI BS EN 556-2 Sterilization of medical devices - Requirements for medical devices to be designated “STERILE” Part 2: Requirements for aseptically processed medical devices
Список продуктов
Данный раздел/документ содержится в продуктах:
Данный раздел/документ содержится в продуктах:
- Техэксперт: Машиностроительный комплекс
- Картотека зарубежных и международных стандартов
- ISO 11137-2 Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose - Second Edition
- 11
- ISO 11137-2 Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose - Second Edition
- 11.080
- ISO 11137-2 Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose - Second Edition
- 11.080.01
- ISO 11137-2 Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose - Second Edition
- ISO 16061 Instrumentation for use in association with non-active surgical implants — General requirements - Second Edition
- CEN EN 556-2 Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devices
- ISO 16061 Instrumentation for use in association with non-active surgical implants — General requirements - Second Edition
- CEN EN 556-2 Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devices
- CEN EN 556-2 Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devices
- CEN EN ISO 11137-1 Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
- BSI BS EN 556-2 Sterilization of medical devices - Requirements for medical devices to be designated “STERILE” Part 2: Requirements for aseptically processed medical devices
- CEN EN ISO 13408-1 Aseptic processing of health care products - Part 1: General requirements
- Картотека зарубежных и международных стандартов
British Standards Institution
Sterilization of medical devices - Requirements for medical devices to be designated “STERILE” Part 2: Requirements for aseptically processed medical devices
N BS EN 556-2
Автоматический перевод:
Обеззараживание медицинских устройств - Требования для медицинских устройств, которые будут определяться “СТЕРИЛЬНАЯ” Часть 2: Требования для стерильным образом обработанных медицинских устройств
Эквиваленты данного стандарта:
- AENOR UNE-EN 556-2 Sterilization of medical devices - Requirements for medical devices to be designated ''STERILE" - Part 2: Requirements for aseptically processed medical devices
- DS DS/EN 556-2 Sterilization of medical devices - Requirements for medical devices to be designated ''STERILE" - Part 2: Requirements for aseptically processed medical devices
- CEN EN 556-2 Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devices
Уважаемый пользователь!
Обратитесь к обслуживающему Вас представителю за дополнительной информацией о возможности приобретения документов указанного разработчика и заказа перевода.
