9 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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EURO-MED LIGHT TOUCH BIOPSY PUNCH
FDA 510(k)
FDA Class 1
·Dental
Invictus
FDA UDI
ALPHATEC SPINE, INC.·00190376242149·Tap, Thoracic, 4.0mm
MODELS 43100A, 43110A & 43120A DEFIBRILLATOR/MONIT
FDA 510(k)
FDA Class 2
·Cardiovascular
PRIMADERM
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
SHILEY
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY TYCO HEALTHCARE·Product code BTO·September 1, 2010
ELLIPSE DR, DF-4 CONNECTOR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·June 19, 2014
ENDOTAK RELIANCE
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVY·July 1, 2015
UNKNOWN ASR XL HEAD
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·October 22, 2010
ACT ARTIC E1 HIP BRG 28X46MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·March 13, 2018