IEC 60601-1-6:2010+A1:2013 specifies a process for a manufacturer toanalyse, specify, design, verify and validate usability, as it relates to basic safety and essential performance of medical electrical equipment. This usability engineering process assessesand mitigates risks caused by usability problems associated with correct use and use errors, i.e., normal use. It can be used to identify but does not assess or mitigate risks associated with abnormal use. If the usability engineering process detailed in thiscollateral standard has been complied with and the acceptance criteria documented in the usability validation plan have been met (see 5.9 of IEC 62366:2007), then the residual risks, as defined in ISO 14971, associated with usability of me equipment are presumed tobe acceptable, unless there is objective evidence to the contrary (see 4.1.2 of IEC 62366:2007). The object of this collateral standard is to specify general requirements that are in addition to those of the general standard and to serve as the basis for particular standards. This document cancels and replaces the secondedition of IEC 60601-1-6 which has been technically revised. It wasrevised to align with the usability engineering process in IEC 62366. To allow for equipment manufacturers and testing organizations to make products and to equip themselves for conducting revised tests in accordance with this third edition, itis recommended by SC 62A that the content of this document not be adopted for mandatory implementation earlier than 3 years from thedate of publication for equipment newly designed and not earlier than 5 years from the date of publication for equipment already inproduction. This consolidated version consists of the third edition (2010) and its amendment 1 (2013). Therefore, no need to order amendment inaddition to this publication.