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English -- Medical Electrical Equipment - Part 2-24: Particular Requirements for the Safety of Infusion Pumps and Controllers - Second Edition;
French -- Appareils électromédicaux - Partie 2-24 : Exigences particulières pour la sécurité de base et les performances essentielles des pompes et régulateurs de perfusion - Second Edition

contributor authorCSA - CSA Group
date accessioned2017-09-04T18:28:14Z
date available2017-09-04T18:28:14Z
date copyright2015.01.01
date issued2015
identifier otherIQBUJFAAAAAAAAAA.pdf
identifier urihttp://mapnamagz.yabesh.ir/std;query=authoF23793FDFCDCAC4/handle/yse/210386
description abstractThis Particular Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of INFUSION PUMPS and VOLUMETRIC INFUSION CONTROLLERS, hereafter referred to as ME EQUIPMENT.
This standard applies to ADMINISTRATION SETS insofar as their characteristics influence the BASIC SAFETY or ESSENTIAL PERFORMANCE of INFUSION PUMPS and VOLUMETRIC INFUSION CONTROLLERS. However this standard does not specify requirements or tests for other aspects of ADMINISTRATION SETS
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 7.2.13 and 8.4.1 of the general standard.
NOTE See also 4.2 of the general standard.
This particular standard specifies the requirements for ENTERAL NUTRITION PUMPS, INFUSION PUMPS, INFUSION PUMPS FOR AMBULATORY USE, SYRINGE OR CONTAINER PUMPS, VOLUMETRIC INFUSION CONTROLLERS and VOLUMETRIC INFUSION PUMPS, as defined in 201.3.204, 201.3.206, 201.3.207, 201.3.220, 201.3.222 and 201.3.223. These particular standard does not apply to the following: a) devices specifically intended for diagnostic or similar use (e.g. angiography or other pumps permanently controlled or supervised by the OPERATOR);
b) devices for extracorporeal circulation of blood;
c) implantable devices;
d) ME EQUIPMENT specifically intended for diagnostic use within urodynamics (measurement of pressure-volume relationship of the urinary bladder when filled through a catheter with water);
e) ME EQUIPMENT specifically intended for diagnostic use within male impotence testing (measurement of amount of liquid infused, necessary to maintain a preset pressure level for maintaining penile erection: cavernosometry, cavernosography);
f) devices covered by ISO 28620.
1 The general standard is IEC 60601-1:2005+A1:2012, Medical electrical equipment – Part 1: General requirements for basic safety and essential performance.
languageEnglish, French
titleCSA CAN/CSA-C22.2 NO. 60601-2-24:15num
titleEnglish -- Medical Electrical Equipment - Part 2-24: Particular Requirements for the Safety of Infusion Pumps and Controllers - Second Editionen
titleFrench -- Appareils électromédicaux - Partie 2-24 : Exigences particulières pour la sécurité de base et les performances essentielles des pompes et régulateurs de perfusion - Second Editionother
typestandard
page150
statusActive
treeCSA - CSA Group:;2015
contenttypefulltext


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