Standard [WITHDRAWN]
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This Collateral Standard specifies the requirements for a process to be carried out by a manufacturer in order to analyse, specify, design, verify and validate usability, as it relates to basic safety and essential performance of medical electrical equipment. Medical electrical equipment is hereafter referred to as ME equipment. The Committee responsible for this standard is Subcommittee UK 811.4 "Ergonomics, usability, instructions of use" of the DKE (German Commission for Electrical, Electronic and Information Technologies) at DIN and VDE.
This document replaces DIN EN 60601-1-6 Berichtigung 1:2010-05; VDE 0750-1-6 Berichtigung 1:2010-05 , DIN EN 60601-1-6:2008-02; VDE 0750-1-6:2008-02 .
This document has been replaced by: DIN EN 60601-1-6:2016-02; VDE 0750-1-6:2016-02 .
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