3 results
·
26ms
·
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 19, 2014
PELORIS RAPID TISSUE PROCESSOR
FDA Adverse Event
LEICA BIOSYSTEMS MELBOURNE·Product code IEO·October 6, 2010
M SERIES
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·November 13, 2012