11 results
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19ms
·
Sources: EU EUDAMED, US FDA
OSSEOSTAP Microdrill System (control unit and handpiece), OSSEOSTAP control unit (foot pedal), OSSEOSTAP handpiece
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
Prime Medical LLC
FDA UDI
Prime Medical LLC·00850055249288·PrimePadPlus-K14-3422
DS ANTERIOR, DS BASE, DS HEAD-NECK, DS HEAD, FLEX (S,M,L)
FDA 510(k)
FDA Class 2
·Radiology
NEXSITE HD (55CM), HEMODIALYSIS CATHETER FOR LONG TERM USE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PS FEMORAL COMPONENT CLOSED BOX LGE RIGHT 74 MM CEMENTED
FDA Adverse Event
Malfunction
·BIOMET SPAIN, S.L.·Product code JWH·June 3, 2020
TAXUS? LIBERTÉ?
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·October 6, 2014
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·June 3, 2013
FREESTYLE FREEDOM LITE
FDA Adverse Event
Injury
·Product code NBW·June 29, 2011
PERF CON TIB BRG LRG 22X60
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code KRR·August 13, 2020
NON-POROUS PERF TIB TRAY-LGE
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code KRR·August 13, 2020
PERF ANAT TIBIAL STEM 120X14X5
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code KRR·August 13, 2020