7 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CONSENSUS POSTERIOR STABILIZED KNEE-INTERCONDYLAR NOTCH ROUTER
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Sklar
FDA UDI
SKLAR CORPORATION·50649111439566·JANSEN NSL FCP BY6.5 STRLCS/25
CONFIDANT 2.0
FDA 510(k)
FDA Class 2
·Cardiovascular
Aortic Arch Cannulae, Optiflow Aortic Arch Cannulae
FDA 510(k)
FDA Class 2
·Cardiovascular
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·February 14, 2013
JOSTENT GRAFTMASTER
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MAF·January 17, 2011
COULTER LH 750 HEMATOLOGY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GKZ·July 28, 2014