3 results
·
25ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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HANCOCK II AORTIC BIOPROSTHETIC HEART VALVE
FDA Adverse Event
Malfunction
·MEDTRONIC HEART VALVES DIVISION·Product code LWR·May 30, 2014
PENUMBRA COIL 400 DETACHMENT HANDLE
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code KRD·November 20, 2012
1527736-2010-00060
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC (CINCINNATI)·Product code GCJ·September 22, 2010