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BS EN 13640:2002
Заменен
Stability testing of in vitro diagnostic reagents
— 14 стр.
Описание
Изменения
Ссылки
Версии
Ссылочные документы
BS EN 375:2001
Заменен
Information supplied by the manufacturer with in vitro diagnostic reagents for professional use
— 18 стр.
BS EN ISO 23640:2011
Заменен
In vitro diagnostic medical devices. Evaluation of stability of in vitro diagnostic reagents
— 14 стр.
На этот документ ссылаются
BS EN ISO 18113-1:2009
Заменен
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). Terms, definitions and general requirements
— 60 стр.
BS EN ISO 15197:2003
Заменен
In vitro diagnostic test systems. Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus
— 46 стр.
BS EN ISO 23640:2013
Заменен
In vitro diagnostic medical devices. Evaluation of stability of in vitro diagnostic reagents
— 16 стр.
BS EN ISO 23640:2011
Заменен
In vitro diagnostic medical devices. Evaluation of stability of in vitro diagnostic reagents
— 14 стр.
BS EN ISO 23640:2015
Действует
In vitro diagnostic medical devices. Evaluation of stability of in vitro diagnostic reagents
— 16 стр.
BS EN ISO 18113-1:2011
Действует
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). Terms, definitions and general requirements
— 62 стр.
BS ISO 17593:2007
Действует
Clinical laboratory testing and in vitro medical devices. Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy
— 64 стр.
BS 6266:2002
Заменен
Code of practice for fire protection for electronic equipment installations
— 38 стр.