3 results
·
36ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
2008K HEMODIALYSIS SYS OLC/DIASAFE PLUS
FDA Adverse Event
Malfunction
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·March 27, 2014
TOTAL ASR FEM IMP SIZE 57
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KXA·November 14, 2012
SYNCHRON LX® I 725 CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code MMI·September 13, 2010