3 results
·
26ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
UNKNOWN DEPUY CEMENT
FDA Adverse Event
Injury
·DEPUY CMW ¿ REG. # 9610921·Product code LOD·January 15, 2013
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HRS·July 7, 2014
HS HAND CONTROLLED CURVED SHEA
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code GEI·February 4, 2008