7 results
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26ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MASTERPIECES MICRO SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756389266·VASCULAR/THYROID PACK
QUELL DESENSITIZER
FDA 510(k)
FDA Class 2
·Dental
M4 MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
HAKIM VALVE
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC.·Product code JXG·November 23, 2010
FLOGARD
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·January 11, 2013
CURRENT PLUS DR, DF-4 CONNECTOR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·July 2, 2014