7 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
PARIETEX UGYTEX PP POSTERIOR KIT X1
FDA Adverse Event
Injury
·SOFRADIM PRODUCTION·Product code FTL·November 7, 2012
2520274-2013-10389
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code MNI·February 28, 2013
PHILIPS
FDA Adverse Event
Death
·PHILIPS MEDICAL SYSTEM NORTH AMERICA CO·Product code KXJ·December 29, 2000
BRANEMARK SYSTEM
FDA Adverse Event
Injury
·NOBEL BIOCARE AB·Product code DZE·August 1, 1997
QUICKIE 2 WHEELCHAIR
FDA Adverse Event
Malfunction
·SUNRISE MEDICAL MPD·Product code IOR·February 17, 1999
SWITCH-BLADE CLICKFIT REUSE HNDL 5MM36CM
FDA Adverse Event
Malfunction
·CAREFUSION·Product code GEI·October 5, 2011
RESTORE ULTRA
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·November 16, 2012