3 results
·
17ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code LDD·June 24, 2014
OCTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·December 28, 2012
ALLEN PAL STIRRUPS
FDA Adverse Event
Other
·ALLEN MEDICAL SYSTEMS·Product code FWZ·November 3, 2010