6 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ADULT RESECTOSCOPE
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
HCT Empty EVA Container Pack
FDA 510(k)
FDA Class 2
·General Hospital
MODEL 1051, MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
RIATA ACTIVE FIXATION
FDA Adverse Event
Injury
·ST. JUDE MEDICAL INC., CRMD·Product code LWS·January 13, 2014
WINGSPAN STENT
FDA Adverse Event
Death
·BOSTON SCIENTIFIC - FREMONT·Product code NJE·November 3, 2010
PROGRASP (TM) FORCEPS
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·December 29, 2012