3 results
·
34ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
HEARTSTART MRX- EMS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 6, 2014
ASPHERE M SPEC 12/14 44 +8.5
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD·Product code KWA·December 30, 2010
AUTOPULSE NIMH BATTERY
FDA Adverse Event
Malfunction
·ZOLL CIRCULATION, INC.·Product code DRM·December 31, 2012