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About This Item
Full Description
This International Standard adds or replaces clauses listed in the IEC 60601-1 that are specific for HIGH INTENSITY THERAPEUTIC ULTRASOUND EQUIPMENT.
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.
Cross References:
IEC 60601-1-2:2007
IEC 61689:2013
IEC/TS 61949
IEC 62127-1
IEC 62127-2
IEC 62359
IEC 62555
IEC/TS 625564
EN 60601-1-2:2007
EN 60601-1-2:2007+corr. March:2010
EN 61689:2013
CLC/TS 61949
EN 62127-1
EN 62127-2
EN 62359
EN 62555
93/42/EEC
IEC 60601-2-5
IEC 60601-2-36
IEC 60050-802
IEC 60529
IEC 61161
IEC 61828
IEC 62649
IEC 62464-1
IEC 62555
IEC/TR 62781
ISO/IEC Guide 98-3:2008
EN 60601-2-5
EN 60601-2-36
EN 60529
EN 61161
EN 61828
EN 62464-1
EN 62555
All current amendments available at time of purchase are included with the purchase of this document.
Document History
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BS EN 60601-2-62:2015
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Medical electrical equipment-Particular requirements for the basic safety and essential performance of high intensity therapeutic ultrasound (HITU) equipment- Most Recent
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BS 12/30191872 DC
BS EN 60601-2-62. Medical electrical equipment. Part 2-62. Particular requirements for basic safety and essential performance of high intensity therapeutic ultrasound (HITU) systems- Historical Version