10 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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IQ SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
APEX PS Knee
FDA UDI
Omni Life Science, Inc.·00841690113546·PS-C Insert, Size 2 x 18mm
Color Cuff
FDA UDI
STRYKER CORPORATION·07613154600199·Non-Sterile Reusable Tourniquet Cuff Single Bla...
Color Cuff
FDA UDI
STRYKER CORPORATION·07613154600182·Non-Sterile Reusable Tourniquet Cuff Single Bla...
Color Cuff
FDA UDI
STRYKER CORPORATION·07613154600175·Non-Sterile Reusable Tourniquet Cuff Single Bla...
ADVANCE TOTAL KNEE SYSTEM-PATELLA
FDA 510(k)
FDA Class 2
·Orthopedic
CADENCE CEMENT RESTRICTOR
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
OPTIFLUX 180NRE DIALYZER FINISHED ASSY.
FDA Adverse Event
Malfunction
·OGDEN MANUFACTURING·Product code FJI·May 23, 2014
HEMABRIDGE WOVEN VASCULAR GRAFT
FDA Adverse Event
Other
·INTERVASCULAR·Product code DSY·January 14, 2013
CONSULTA
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL, INC.·Product code NIK·December 13, 2010