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DIN EN ISO 18113-3:2013-01

Действует
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009); German version EN ISO 18113-3:2011 — 18 стр.
ОписаниеИзмененияСсылкиВерсии

Ссылочные документы

ÖNORM EN ISO 14971:2013-03
Заменен
Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01)
ÖNORM EN ISO 15223-1:2012-10
Заменен
Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements (ISO 15223-1:2012)
DIN EN ISO 14971:2009-10
Отменен
Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01); German version EN ISO 14971:2009 — 103 стр.
DIN EN ISO 18113-1:2013-01
Действует
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009); German version EN ISO 18113-1:2011 — 60 стр.
DIN EN ISO 18113-2:2013-01
Действует
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009); German version EN ISO 18113-2:2011 — 19 стр.
DIN EN 591:2001-07
Отменен
Instructions for use for in-vitro-diagnostic instruments for professional use; German version EN 591:2001 — 11 стр.
ÖNORM EN 980:2008-08
Заменен
Symbols for use in the labelling of medical devices
DIN EN ISO 18113-3:2010-05
Отменен
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009); German version EN ISO 18113-3:2009 — 19 стр.

На этот документ ссылаются

DIN EN ISO 18113-2:2013-01
Действует
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009); German version EN ISO 18113-2:2011 — 19 стр.
DIN EN ISO 18113-3:2010-05
Отменен
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009); German version EN ISO 18113-3:2009 — 19 стр.
DIN EN ISO 18113-2:2010-05
Отменен
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009); German version EN ISO 18113-2:2009 — 22 стр.
DIN EN ISO 15223-1:2012-10
Отменен
Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements (ISO 15223-1:2012); German version EN ISO 15223-1:2012, with CD-ROM — 43 стр.
DIN EN ISO 15223-1:2013-02
Отменен
Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements (ISO 15223-1:2012); German version EN ISO 15223-1:2012, with CD-ROM — 36 стр.
DIN EN ISO 15223-1:2017-04
Отменен
Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements (ISO 15223-1:2016, Corrected version 2017-03); German version EN ISO 15223-1:2016, with CD-ROM — 47 стр.