3 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
HEARTSTREAM FR2
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 11, 2014
AUTOPULSE NIMH BATTERY
FDA Adverse Event
Malfunction
·ZOLL CIRCULATION INC·Product code DRM·January 25, 2013
840
FDA Adverse Event
Malfunction
·COVIDIEN PURITAN-BENNETT·Product code CBK·January 11, 2011