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CSA CAN/CSA-C22.2 NO. 80601-2-30-10

English -- Medical electrical equipment — Part 2-30: Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers - First Edition; Incorporates Corrigendum 1: June 2011;
French -- Appareils électromédicaux — Partie 2-30 : Exigences particulières pour la sécurité de base et les performances essentielles des sphygmomanomètres non invasifs automatiques - First Edition; Incorporates Corrigendum 1: June 2011

Organization:
CSA - CSA Group
Year: 2010

Abstract: Replacement:
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of AUTOMATED SPHYGMOMANOMETERS, hereafter referred to as ME EQUIPMENT, which by means of an inflatable CUFF, are used for intermittent indirect measurement of the BLOOD PRESSURE without arterial puncture.
NOTE 1 Equipment that performs indirect measurement of the BLOOD PRESSURE without arterial puncture does not directly measure the BLOOD PRESSURE. It only estimates the BLOOD PRESSURE.
This standard specifies requirements for the BASIC SAFETY and ESSENTIAL PERFORMANCE for this ME EQUIPMENT and its ACCESSORIES, including the requirements for the accuracy of a DETERMINATION.
This standard covers electrically-powered intermittent, indirect measurement of the BLOOD PRESSURE without arterial puncture, ME EQUIPMENT with automatic methods for estimating BLOOD PRESSURE, including BLOOD PRESSURE monitors for the HOME HEALTHCARE ENVIRONMENT.
Requirements for indirect measurement of the BLOOD PRESSURE without arterial puncture ME EQUIPMENT with an electrically-powered PRESSURE TRANSDUCER and/or displays used in conjunction with a stethoscope or other manual methods for determining BLOOD PRESSURE (NON-AUTOMATED SPHYGMOMANOMETERS) are specified in document ISO 81060-1.
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 standard are not covered by specific requirements in this standard except in 201.11 and 201.105.3.3, as well as 7.2.13 and 8.4.1 of IEC 60601-1.
NOTE 2 See also 4.2 of the general standard.
URI: http://mapnamagz.yabesh.ir/std;query=authoF23793FDFCDCAC4/handle/yse/209889
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    CSA CAN/CSA-C22.2 NO. 80601-2-30-10

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contributor authorCSA - CSA Group
date accessioned2017-09-04T18:27:41Z
date available2017-09-04T18:27:41Z
date copyright2010.01.01
date issued2010
identifier otherIORSMEAAAAAAAAAA.pdf
identifier urihttp://mapnamagz.yabesh.ir/std;query=authoF23793FDFCDCAC4/handle/yse/209889
description abstractReplacement:
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of AUTOMATED SPHYGMOMANOMETERS, hereafter referred to as ME EQUIPMENT, which by means of an inflatable CUFF, are used for intermittent indirect measurement of the BLOOD PRESSURE without arterial puncture.
NOTE 1 Equipment that performs indirect measurement of the BLOOD PRESSURE without arterial puncture does not directly measure the BLOOD PRESSURE. It only estimates the BLOOD PRESSURE.
This standard specifies requirements for the BASIC SAFETY and ESSENTIAL PERFORMANCE for this ME EQUIPMENT and its ACCESSORIES, including the requirements for the accuracy of a DETERMINATION.
This standard covers electrically-powered intermittent, indirect measurement of the BLOOD PRESSURE without arterial puncture, ME EQUIPMENT with automatic methods for estimating BLOOD PRESSURE, including BLOOD PRESSURE monitors for the HOME HEALTHCARE ENVIRONMENT.
Requirements for indirect measurement of the BLOOD PRESSURE without arterial puncture ME EQUIPMENT with an electrically-powered PRESSURE TRANSDUCER and/or displays used in conjunction with a stethoscope or other manual methods for determining BLOOD PRESSURE (NON-AUTOMATED SPHYGMOMANOMETERS) are specified in document ISO 81060-1.
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 standard are not covered by specific requirements in this standard except in 201.11 and 201.105.3.3, as well as 7.2.13 and 8.4.1 of IEC 60601-1.
NOTE 2 See also 4.2 of the general standard.
languageEnglish, French
titleCSA CAN/CSA-C22.2 NO. 80601-2-30-10num
titleEnglish -- Medical electrical equipment — Part 2-30: Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers - First Edition; Incorporates Corrigendum 1: June 2011en
titleFrench -- Appareils électromédicaux — Partie 2-30 : Exigences particulières pour la sécurité de base et les performances essentielles des sphygmomanomètres non invasifs automatiques - First Edition; Incorporates Corrigendum 1: June 2011other
typestandard
page140
statusActive
treeCSA - CSA Group:;2010
contenttypefulltext
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DSpace software copyright © 2017-2020  DuraSpace
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