3 results
·
15ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
ADVIA 2120 WITH DUAL ASPIRATE
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code GKZ·November 21, 2012
M SERIES
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·June 8, 2015
ESSURE
FDA Adverse Event
Malfunction
·BAYER PHARMA AG·Product code HHS·September 17, 2010