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These particular requirements applies to the basic safety and essential performance of multifunction patient monitoring equipment. They supplement DIN EN 60601-1:2007 and the associated supplementary standards. The main features are the adaptation to the new structure of DIN EN 60601-1:2007, revision of the requirements for alarms based on DIN EN 60601-1-8:2008-02 and the EMC tests based on DIN EN 60601-1-2:2007-12. The responsible committee is Subcommittee DKE/UK 812.1 "Diagnostik" ("Diagnostics") of the DKE (German Commission for Electrical, Electronic and Information Technologies) at DIN and VDE.
This document replaces DIN EN 60601-2-49:2002-12; VDE 0750-2-49:2002-12 .
This document has been replaced by: DIN EN IEC 80601-2-49:2020-10; VDE 0750-2-49:2020-10 .