3 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
PROTECTA XT CRT-D
FDA Adverse Event
Malfunction
·IPG MFG SWITZERLAND·Product code NIK·February 9, 2013
UNKNOWN HEAD
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LPH·July 23, 2014
KIMVENT* MICROCUFF* ENDOTRACHEAL TUBE
FDA Adverse Event
Malfunction
·KIMBERLY-CLARK HEALTH CARE·Product code BTR·January 7, 2011