9 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Medline UNITE® REFLEX® Nitinol Staple Kit
FDA 510(k)
FDA Class 2
·Orthopedic
3DKNEE POROUS COATED FEMORAL COMPONENT
FDA 510(k)
FDA Class 2
·Orthopedic
200 MICRON BLOOD COMPONENT FILTER AND SYRINGE ADAPTER
FDA 510(k)
FDA Class 2
·General Hospital
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 21, 2025
RECONSTRUCTION NAIL R1.5, TI, LEFT T2 RECON ?11X34
FDA Adverse Event
Injury
·STRYKER TRAUMA GMBH·Product code HSB·December 19, 2012
TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORP.·Product code NIQ·February 1, 2007
FLO-GARD 6201 VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE (SG)·Product code FRN·November 18, 2008
COLLEAGUE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 2, 2011
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
Malfunction
·INVAMEX·Product code IOR·July 18, 2013