Revidiran
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.
POVUČEN
IEC 60601-1-6:2004 ED1
POVUČEN
IEC 60601-1-6:2006 ED2
99.60
Povlačenje stupilo na snagu
27. 1. 2010.
OBJAVLJEN
IEC 60601-1-6:2010 ED3