3 results
·
14ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
TRILOGY 200
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code CBK·April 16, 2014
LIFEPAK(R) 12 DEFIBRILLATOR/MONITOR SERIES
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code MKJ·December 3, 2012
RESTORE ULTRA
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·September 7, 2010