8 results
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28ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LIGAFIX INTERFACE SCREW
FDA 510(k)
FDA Class 2
·Orthopedic
LEONE SPA
FDA UDI
LEONE SPA·08033707065715·INTRAORAL ELASTICS 4,5 oz 5/16" blue
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450225493·
BIPAP DUET LX BI-LEVEL SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
TAKE ONE BITE MODIFIED
FDA 510(k)
FDA Class 2
·Dental
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 2, 2013
DEPUY ASR XL FEM IMP SIZE 43
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD - 8010379·Product code KXA·September 16, 2014
SM104 M-SERIES W/5TH WHEEL
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FPO·May 11, 2011