ÍST EN ISO 80601-2-55:2011

Staða:

Fellur úr gildi - 15.6.2018

Íslenskt heiti:

Rafmagnslækningatæki – Hluti 2-55: Sérstakar kröfur um almennt öryggi og áskilið nothæfi vöktunarbúnaðar til að greina öndunarloft

Enskt heiti:

Medical electrical equipment - Part 2-55: Particular requirements for the basic safety and essential performanceof respiratory gas monitors

Tengdur staðall:

ISO 80601-2-55:2011

Tækninefnd:

CEN/TC 215

ICS flokkur:

11.04

Auglýst:

18.6.2018

Umfang (scope):

Rafmagnslækningatæki – Hluti 2-55: Sérstakar kröfur um almennt öryggi og áskilið nothæfi vöktunarbúnaðar til að greina öndunarloft

Hafðu samband í síma 520-7150 varðandi þennan staðal.

* Mynd sem fylgir ÍST EN ISO 21647:2009

ÍST EN ISO 21647:2009

Rafmagnslækningatæki - Sérstakar kröfur um almennt öryggi og áskilið nothæfi vöktunarbúnaðar til að greina öndunarloft
Verð: 13.594 kr.
* Mynd sem fylgir ÍST EN ISO 80601-2-55:2018

ÍST EN ISO 80601-2-55:2018

ISO 80601-2-55:2018 specifies particular requirements for the basic safety and essential performance of a respiratory gas monitor (rgm), hereafter referred to as me equipment, intended for continuous operation for use with a patient. ISO 80601-2-55:2018 specifies requirements for - anaesthetic gas monitoring, - carbon dioxide monitoring, and - oxygen monitoring. NOTE 1 An rgm can be either stand-alone me equipment or integrated into other equipment, e.g. an anaesthetic workstation or a ventilator. ISO 80601-2-55:2018 is not applicable to an rgm intended for use with flammable anaesthetic agents. If a clause or subclause is specifically intended to be applicable to me equipment only or to me systems only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to me equipment and to me systems, as relevant. Hazards inherent in the intended physiological function of me equipment or me systems within the scope of this do
Verð: 16.956 kr.
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