Specifies requirements for a process to analyse, design, verify and validate the usability, as it relates to basic safety and essential performance of medical electrical equipment. This collateral standard addresses normal use and use errors but excludes abnormal use. The object of this collateral standard is to specify general requirements that are in addition to those of the general standard IEC 60601-1 and to serve as the basis for particular standards.
Legislation related to this standard
WITHDRAWN
EN 60601-1-6:2004
WITHDRAWN
EN 60601-1-6:2007
99.60
Withdrawal effective
Apr 1, 2013
WITHDRAWN
EN 60601-1-6:2007/corrigendum Mar. 2010
PUBLISHED
EN 60601-1-6:2010