Стандарты BSI

BS EN 376:2002

Заменен

Information supplied by the manufacturer with in vitro diagnostic reagents for self-testing — 18 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 592:2002

Заменен

Instructions for use for in vitro diagnostic instruments for self-testing — 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 ISO 7000:2004

Действует

Graphical symbols for use on equipment. Index and synopsis — 212 стр.

BS ISO 10006:2003

Заменен

Quality management systems. Guidelines for quality management in projects — 42 стр.

BS EN ISO 18113-4:2009

Заменен

In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). In vitro diagnostic reagents for self-testing — 22 стр.

На этот документ ссылаются

BS EN 592:2002

Заменен

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

BS EN 980:2003

Заменен

Graphical symbols for use in the labelling of medical devices — 28 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 18113-4:2009

Заменен

In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). In vitro diagnostic reagents for self-testing — 22 стр.

BS EN 980:2008

Заменен

Symbols for use in the labelling of medical devices — 38 стр.

BS EN 12376:1999

Заменен

In vitro diagnostic medical devices. Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology — 14 стр.

BS EN ISO 18113-4:2011

Действует

In vitro diagnostic medical Devices. Information supplied by the manufacturer (labelling). In vitro diagnostic reagents for self-testing — 24 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 EN 13612:2002

Действует

Performance evaluation of in vitro diagnostic medical devices — 18 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 376:1992

Заменен

Specification for labelling of in vitro diagnostic reagents for self-testing — 14 стр.

ÖNORM EN 13641:2002-07

Действует

Elimination or reduction of risk of infection related to in vitro diagnostic reagents

ÖNORM EN 13532:2002-08

Действует

General requirements for in vitro diagnostic medical devices for self-testing