6 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
BUCKET PROSTHESIS PORP
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
SPECTRON PRIMARY STEM FEMORAL PROSTHES
FDA 510(k)
FDA Class 2
·Orthopedic
STINGRAY GUIDEWIRE, STIFF, MODELS M-3003, M-3004, M-3011, M-3012
FDA 510(k)
FDA Class 2
·Cardiovascular
CORE IMPACTION DRILL
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS-KALAMAZOO·Product code DZJ·June 19, 2014
ECHELON* 60 ENDOPATH**
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·October 27, 2010
COBAS E411 RACK SYSTEM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JLW·December 21, 2012