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IEC 60601-1 and IEC 60601-1-2 Medical Electrical Equipment Package

IEC 60601-1 and IEC 60601-1-2 Medical Electrical Equipment Package

IEC 60601-1 and IEC 60601-1-2 Medical Electrical Equipment Package provide the general requirements for basic safety and essential performance of medical electrical equipment and medical electrical systems. The general requirements of medical electrical equipment includes testing, classification, identification / marking and protection against electrical hazards. The IEC 60601-1 and IEC 60601-1-2 Medical Electrical Equipment Package specifically address the electromagnetic compatibility of medcial electrical equipment. This package includes:
 IEC 60601-1 Ed. 3.0 b:2005
 IEC 60601-1 Ed. 3.0 b Cor.1:2006
 IEC 60601-1 Ed. 3.0 b Cor.2:2007
 IEC 60601-1 Amd.1 Ed. 3.0 b:2012
 IEC 60601-1 Ed. 3.1 en:2012
 IEC 60601-1 Amd.1 Ed. 3.0 b Cor.1:2014
 IEC 60601-1 Amd.2 Ed. 3.0 en:2020
 IEC 60601-1-2 Ed. 4.0 b:2014
 IEC 60601-1-2 Amd.1 Ed. 4.0 en:2020

IEC 60601-1 and IEC 60601-1-2 Medical Electrical Equipment Package includes:


Content Provider
International Electrotechnical Commission [IEC]


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As the voice of the U.S. standards and conformity assessment system, the American National Standards Institute (ANSI) empowers its members and constituents to strengthen the U.S. marketplace position in the global economy while helping to assure the safety and health of consumers and the protection of the environment.

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