9 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ORTHOFIX TIBIAL NAILING SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
NexGen®
FDA UDI
Zimmer, Inc.·00889024209947·
NexGen®
FDA UDI
Zimmer, Inc.·00889024209923·
NexGen®
FDA UDI
Zimmer, Inc.·00889024209930·
AUTO-TOTAL BILIRUBIN REAG FOR GILFORD AN
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Cadwell AmpliScan
FDA 510(k)
FDA Class 2
·Neurology
HEARTSTART MRX-EMS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·January 15, 2013
CODMAN EXTERNAL DRAINAGE SYSTEM III
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC·Product code JXG·January 11, 2011
EON MINI
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·July 22, 2014