Revidiran
specifies minimum requirements for immunity and emissions regarding electromagnetic compatibility for in vitro diagnostic medical equipment, taking into account the particularities and specific aspects of this electrical equipment and their electromagnetic environment.
The contents of the corrigendum of September 2007 have been included
in this copy.
POVUČEN
IEC 61326-2-6:2005 ED1
99.60
Povlačenje stupilo na snagu
10. 7. 2012.
POVUČEN
IEC 61326-2-6:2005/COR1:2007 ED1
POVUČEN
IEC 61326-2-6:2012 ED2