3 results
·
14ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
MICROSPAN SYSTEM
FDA Adverse Event
Malfunction
·ETHICON, INC.·Product code FED·June 8, 2006
HEARTSTART XL + DEFIBRILLATOR/MONITOR
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·January 16, 2013
MEGA SUTURECUT NEEDLE DRIVER INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·July 28, 2014