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EVS-EN ISO 80601-2-56:2017+A1:2020

Elektrilised meditsiiniseadmed. Osa 2-56: Erinõuded kehatemperatuuri mõõtmise kliiniliste termomeetrite esmasele ohutusele ja olulistele toimimisnäitajatele

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Kehtiv alates 02.06.2020
Alusdokumendid
ISO 80601-2-56:2017; EN ISO 80601-2-56:2017; ISO 80601-2-56:2017/Amd 1:2018; EN ISO 80601-2-56:2017/A1:2020
Tegevusala (ICS grupid)
11.040.55 Diagnostikaseadmed
Direktiivid või määrused
puuduvad
Standardi ajalugu
Staatus
Kuupäev
Tüüp
Nimetus
02.06.2020
Põhitekst + muudatus
02.08.2017
Põhitekst
This document applies to the basic safety and essential performance of a clinical thermometer in combination with its accessories, hereafter referred to as me equipment. This document specifies the general and technical requirements for electrical clinical thermometers. This document applies to all electrical clinical thermometers that are used for measuring the body temperature of patients. Clinical thermometers can be equipped with interfaces to accommodate secondary indicators, printing equipment, and other auxiliary equipment to create me systems. This document does not apply to auxiliary equipment. Me equipment that measures and displays a body temperature is inside the scope of this document. EXAMPLE 1 Me equipment using accessories such as a pulmonary artery catheter for the determination of cardiac output by thermodilution is in the scope of this document if it displays a body temperature. EXAMPLE 2 Me equipment using accessories such as a Foley catheter that includes a temperature probe is in the scope of this document. This document does not specify the requirements for screening thermographs intended to be used for the individual non-invasive human febrile temperature screening of groups of individual humans under indoor environmental conditions, which are given in IEC 80601-2-59[4]. 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 document are not covered by specific requirements in this document except in IEC 60601-1:2005+A1:2012, 7.2.13 and 8.4.1. NOTE Additional information can be found in IEC 60601-1:2005+A1:2012, 4.2.
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EVS-EN ISO 80601-2-61:2019

Elektrilised meditsiiniseadmed. Osa 2-61: Erinõuded meditsiiniotstarbelise pulssoksümeetri esmasele ohutusele ja olulistele toimimisnäitajatele
Uusim versioon Kehtiv alates 15.02.2019
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EVS-EN 60601-2-47:2015

Elektrilised meditsiiniseadmed. Osa 2-47: Erinõuded ambulatoorsete elektrokardiograafiasüsteemide esmasele ohutusele ja olulistele toimimisnäitajatele
Uusim versioon Kehtiv alates 08.06.2015
Põhitekst + muudatus

EVS-EN 60601-1:2006+A1:2013+A12:2014

Elektrilised meditsiiniseadmed. Osa 1: Üldised nõuded esmasele ohutusele ja olulistele toimimisnäitajatele
Uusim versioon Kehtiv alates 02.03.2016
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EVS-EN ISO/IEEE 11073-10201:2020

Health informatics - Device interoperability - Part 10201: Point-of-care medical device communication - Domain information model (ISO/IEEE 11073-10201:2020)
Uusim versioon Kehtiv alates 15.06.2020