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BS EN 592:2002

Заменен
Instructions for use for in vitro diagnostic instruments for self-testing — 14 стр.
ОписаниеИзмененияСсылкиВерсии

Ссылочные документы

BS EN 375:2001
Заменен
Information supplied by the manufacturer with in vitro diagnostic reagents for professional use — 18 стр.
BS EN 376:2002
Заменен
Information supplied by the manufacturer with in vitro diagnostic reagents for self-testing — 18 стр.
BS EN 591:2001
Заменен
Instructions for use for in vitro diagnostic instruments for professional use — 14 стр.
BS EN 980:2003
Заменен
Graphical symbols for use in the labelling of medical devices — 28 стр.
BS EN 28601:1992
Действует
Specification for representation of dates and times in information interchange — 24 стр.
BS EN 61010-1:1993
Заменен
Safety requirements for electrical equipment for measurement, control and laboratory use, General requirements — 110 стр.
BS ISO 10006:2003
Заменен
Quality management systems. Guidelines for quality management in projects — 42 стр.
BS EN ISO 18113-5:2009
Заменен
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). In vitro diagnostic instruments for self-testing — 20 стр.

На этот документ ссылаются

BS EN 376:2002
Заменен
Information supplied by the manufacturer with in vitro diagnostic reagents for self-testing — 18 стр.
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 18113-5:2009
Заменен
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). In vitro diagnostic instruments for self-testing — 20 стр.
BS EN 980:2008
Заменен
Symbols for use in the labelling of medical devices — 38 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 1041:2008
Действует
Information supplied by the manufacturer of medical devices — 28 стр.
BS EN 61010-2-101:2002
Заменен
Safety requirements for electrical equipment for measurement, control and laboratory use. Particular requirements for in vitro diagnostic (IVD) medical equipment — 26 стр.
BS EN ISO 18113-5:2011
Действует
In vitro diagnostic medical Devices. Information supplied by the manufacturer (labelling). In vitro diagnostic instruments for self-testing — 22 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 EN 13532:2002
Действует
General requirements for in vitro diagnostic medical devices for self-testing — 12 стр.
BS EN 1041:2008+A1:2013
Действует
Information supplied by the manufacturer of medical devices — 28 стр.
BS EN 592:1995
Заменен
Specification for user manuals for in vitro diagnostic instruments for home use — 12 стр.
ÖNORM EN 13532:2002-08
Действует
General requirements for in vitro diagnostic medical devices for self-testing