3 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
7900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·April 16, 2014
PULSAR GENERATOR
FDA Adverse Event
Malfunction
·MEDTRONIC ADVANCED ENERGY LLC·Product code GEI·October 25, 2012
KEEPSAFE DELUXE NO POWER SWITCH
FDA Adverse Event
Malfunction
·J. T. POSEY CO.·Product code KMI·August 26, 2010