ISO 3826-4 Plastics collapsible containers for human blood and blood components - Part 4: Aphaeresis blood bag systems with integrated features - First Edition
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Данный раздел/документ содержится в продуктах:
Данный раздел/документ содержится в продуктах:
- Техэксперт: Машиностроительный комплекс
- Картотека зарубежных и международных стандартов
- ISO 3826-4 Plastics collapsible containers for human blood and blood components - Part 4: Aphaeresis blood bag systems with integrated features - First Edition
- 11
- ISO 3826-4 Plastics collapsible containers for human blood and blood components - Part 4: Aphaeresis blood bag systems with integrated features - First Edition
- 11.040
- ISO 3826-4 Plastics collapsible containers for human blood and blood components - Part 4: Aphaeresis blood bag systems with integrated features - First Edition
- 11.040.20
- ASTM E691 Standard Practice for Conducting an Interlaboratory Study to Determine the Precision of a Test Method
- ASTM D5458 Standard Test Method for Peel Cling of Stretch Wrap Film
- ASTM D4649 Standard Guide for Selection and Use of Stretch Wrap Films
- ASTM D5414 Standard Test Method for Evaluation of Horizontal Impact Performance of Load Unitizing Stretch Wrap Films
- ASTM D4169 Standard Practice for Performance Testing of Shipping Containers and Systems
- UL 61010-2-101 BULLETIN UL Standard for Safety Electrical Equipment for Measurement, Control, and Laboratory Use – Part 2-101: Particular Requirements for In Vitro Diagnostic (IVD) Medical Equipment - COMMENTS DUE: JULY 27, 2015
- ISO 15223-1 Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements - Second Edition
- UL 61010-2-101 BULLETIN UL Standard for Safety Electrical Equipment for Measurement, Control, and Laboratory Use – Part 2-101: Particular Requirements for In Vitro Diagnostic (IVD) Medical Equipment - COMMENTS DUE: JULY 27, 2015
- ASTM D4169 Standard Practice for Performance Testing of Shipping Containers and Systems
- ASTM D5414 Standard Test Method for Evaluation of Horizontal Impact Performance of Load Unitizing Stretch Wrap Films
- ASTM D4649 Standard Guide for Selection and Use of Stretch Wrap Films
- ASTM D5458 Standard Test Method for Peel Cling of Stretch Wrap Film
- ASTM D5458 Standard Test Method for Peel Cling of Stretch Wrap Film
- ASTM D4649 Standard Guide for Selection and Use of Stretch Wrap Films
- ASTM D5414 Standard Test Method for Evaluation of Horizontal Impact Performance of Load Unitizing Stretch Wrap Films
- ASTM D4169 Standard Practice for Performance Testing of Shipping Containers and Systems
- UL 61010-2-101 BULLETIN UL Standard for Safety Electrical Equipment for Measurement, Control, and Laboratory Use – Part 2-101: Particular Requirements for In Vitro Diagnostic (IVD) Medical Equipment - COMMENTS DUE: JULY 27, 2015
- ISO 15223-1 Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements - Second Edition
- UL 61010-2-101 BULLETIN UL Standard for Safety Electrical Equipment for Measurement, Control, and Laboratory Use – Part 2-101: Particular Requirements for In Vitro Diagnostic (IVD) Medical Equipment - COMMENTS DUE: JULY 27, 2015
- ASTM D4169 Standard Practice for Performance Testing of Shipping Containers and Systems
- ASTM D5414 Standard Test Method for Evaluation of Horizontal Impact Performance of Load Unitizing Stretch Wrap Films
- ASTM D4649 Standard Guide for Selection and Use of Stretch Wrap Films
- ASTM D4649 Standard Guide for Selection and Use of Stretch Wrap Films
- ASTM D5414 Standard Test Method for Evaluation of Horizontal Impact Performance of Load Unitizing Stretch Wrap Films
- ASTM D4169 Standard Practice for Performance Testing of Shipping Containers and Systems
- UL 61010-2-101 BULLETIN UL Standard for Safety Electrical Equipment for Measurement, Control, and Laboratory Use – Part 2-101: Particular Requirements for In Vitro Diagnostic (IVD) Medical Equipment - COMMENTS DUE: JULY 27, 2015
- ISO 15223-1 Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements - Second Edition
- UL 61010-2-101 BULLETIN UL Standard for Safety Electrical Equipment for Measurement, Control, and Laboratory Use – Part 2-101: Particular Requirements for In Vitro Diagnostic (IVD) Medical Equipment - COMMENTS DUE: JULY 27, 2015
- ASTM D4169 Standard Practice for Performance Testing of Shipping Containers and Systems
- ASTM D5414 Standard Test Method for Evaluation of Horizontal Impact Performance of Load Unitizing Stretch Wrap Films
- ASTM D5414 Standard Test Method for Evaluation of Horizontal Impact Performance of Load Unitizing Stretch Wrap Films
- ASTM D4169 Standard Practice for Performance Testing of Shipping Containers and Systems
- UL 61010-2-101 BULLETIN UL Standard for Safety Electrical Equipment for Measurement, Control, and Laboratory Use – Part 2-101: Particular Requirements for In Vitro Diagnostic (IVD) Medical Equipment - COMMENTS DUE: JULY 27, 2015
- ISO 15223-1 Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements - Second Edition
- UL 61010-2-101 BULLETIN UL Standard for Safety Electrical Equipment for Measurement, Control, and Laboratory Use – Part 2-101: Particular Requirements for In Vitro Diagnostic (IVD) Medical Equipment - COMMENTS DUE: JULY 27, 2015
- ASTM D4169 Standard Practice for Performance Testing of Shipping Containers and Systems
- ASTM D4169 Standard Practice for Performance Testing of Shipping Containers and Systems
- UL 61010-2-101 BULLETIN UL Standard for Safety Electrical Equipment for Measurement, Control, and Laboratory Use – Part 2-101: Particular Requirements for In Vitro Diagnostic (IVD) Medical Equipment - COMMENTS DUE: JULY 27, 2015
- ISO 15223-1 Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements - Second Edition
- UL 61010-2-101 BULLETIN UL Standard for Safety Electrical Equipment for Measurement, Control, and Laboratory Use – Part 2-101: Particular Requirements for In Vitro Diagnostic (IVD) Medical Equipment - COMMENTS DUE: JULY 27, 2015
- UL 61010-2-101 BULLETIN UL Standard for Safety Electrical Equipment for Measurement, Control, and Laboratory Use – Part 2-101: Particular Requirements for In Vitro Diagnostic (IVD) Medical Equipment - COMMENTS DUE: JULY 27, 2015
- ISO 15223-1 Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements - Second Edition
- ISO 15223-1 Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements - Second Edition
- ISO IWA 23 Interoperability of microfluidic devices - Guidelines for pitch spacing dimensions and initial device classification - First Edition
- Картотека зарубежных и международных стандартов
Ссылается на
- В списке элементов: 17
- ISO 15223-1 Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements - Third EditionМедицинские устройства - Символы, которые будут использоваться с метками медицинского устройства, маркировкой и информацией, которая будет поставляться - Часть 1: Общие требования - Третий Выпуск
Карточка документа - ISO 1135-4 Transfusion equipment for medical use - Part 4: Transfusion sets for single use, gravity feed - Sixth EditionОборудование переливания для медицинского использования - Часть 4: Переливание устанавливает для единственного использования, подачи самотеком - Шестой Выпуск
Карточка документа - ISO 3826-1 Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers - Second EditionПроизводство сборно-разборные контейнеры для человеческой крови и компонентов крови - Часть 1: стандартные контейнеры - второе издание
Карточка документа - ISO 8536-4 AMD 1 Infusion equipment for medical use - Part 4: Infusion sets for single use, gravity feed AMENDMENT 1 - Fifth EditionОборудование вливания для медицинского использования - Часть 4: Вливание устанавливает для единственного использования, AMENDMENT 1 подачи силы тяжести - Пятый 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 23908 Sharps injury protection — Requirements and test methods — Sharps protection features for single-use hypodermic needles, introducers for catheters and needles used for blood sampling - First EditionЗащита раны Sharps — Требования и методы испытаний — защита Sharps показывают для игл шприца единственного использования, introducers для катетеров и игл, используемых для забора крови - Первый Выпуск
Карточка документа - CEN EN 15986 Symbol for use in the labelling of medical devices - Requirements for labelling of medical devices containing phthalatesСимвол для использования в маркировке медицинских устройств - Требования для маркировки медицинских устройств, содержащих фталаты
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 - ISO 15747 Plastic containers for intravenous injections - Second EditionПластмассовые контейнеры для внутривенных инжекций - Второй Выпуск
Карточка документа - ISO 10993-5 Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity - Third EditionБиологическая оценка медицинских устройств - Часть 5: Анализы на в пробирке цитотоксичность - Третий Выпуск
Карточка документа - ISO 3826-2 Plastics collapsible containers for human blood and blood components — Part 2: Graphical symbols for use on labels and instruction leaflets - First EditionПроизводство пластмассовых сборно-разборные контейнеры для человеческой крови и компонентов крови — Часть 2: графические символы для использования на этикетках и инструкции листовки - первое издание
Карточка документа - ISO 3826-3 Plastics collapsible containers for human blood and blood components Part 3: Blood bag systems with integrated features - First EditionПластмассовые сборно-разборные контейнеры для человеческой крови и компонентов крови Часть 3: системы мешок для крови со встроенной особенности - первое издание
Карточка документа - 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 10993-4 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 594-2 Conical Fittings with a 6 % (Luer) Taper for Syringes, Needles and Certain Other Medical Equipment - Part 2: Lock Fittings - Second EditionКонические детали с 6% (Luer) тонкая свеча для сиринксов, иглы и определенное другое медицинское оборудование - часть 2: детали замка - второй выпуск
Карточка документа - ISO 3696 Water for Analytical Laboratory Use - Specification and Test Methods - First EditionВода для аналитического лабораторного использования - спецификации и методов испытаний - первый выпуск
На основе ISO 3696 разработан ГОСТ Р 52501-2005 (MOD)ГОСТ Р 52501-2005 (MOD)
