12 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
CONMED
FDA Adverse Event
Malfunction
·CONMED CORPORATION·Product code LKF·January 5, 2012
CONMED
FDA Adverse Event
Malfunction
·CONMED CORPORATION·Product code LKF·January 5, 2012
DA+ T SERIES DR
FDA Adverse Event
Injury
·MEDTRONIC S.A.·Product code DXY·June 10, 2010
MULTIFUNCTION INSTRUMENT SYSTEM (STRAIGHT GRIP HANDLE)
FDA Adverse Event
Malfunction
·CONMED CORP·Product code GEI·December 6, 2001
INSYNC SENTRY
FDA Adverse Event
Injury
·MEDTRONIC S.A.·Product code NIK·June 11, 2010
EDWARDS SAPIEN 3 TRANSCATHETER HEART VALVE / P140031
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·August 30, 2023
EDWARDS SAPIEN 3 TRANSCATHETER HEART VALVE / P140031
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·August 10, 2023
DEXTRUS 4136
FDA Adverse Event
Injury
·BIOTRONIK SE & CO. KG·Product code NVN·May 13, 2013
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·September 23, 2014
STEALTHSTATION TREON TREATMENT GUIDANCE SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC.·Product code HAW·May 17, 2011
EDWARDS SAPIEN 3 ULTRA TRANSCATHETER HEART VALVE / P140031
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·March 6, 2024
EDWARDS SAPIEN 3 ULTRA RESILIA TRANSCATHETER HEART VALVE / P140031
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·August 6, 2024