7 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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KARL STORZ MICRO-INSTRUMENT FOR COCHLEAR IMPLANTATION
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704269000·
DIAGNOSTIC ULTRASOUND SYSTEM, TYPE 3535, MODIFIED
FDA 510(k)
FDA Class 2
·Radiology
MODEL FORTY ULTRA COMPACT VIDEO IMAGER
FDA 510(k)
FDA Class 2
·Radiology
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·February 6, 2013
WALLFLEX BILIARY RX FULLY-COVERED STENT SYSTEM, MODEL M00570500,M00570510, M0057
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code FGE·January 4, 2011
MALLINCKRODT
FDA Adverse Event
Injury
·COVIDIEN.·Product code JOH·July 10, 2014