7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SENOGRAPHE PEARL AND SENOGRAPHE SAPPHIRE
FDA 510(k)
FDA Class 2
·Radiology
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690185413·Revision Knee Spiral Reamer- Hudson Short Flute...
ANS 90 CM AND 110 CM (3100 AND 3200 SERIES) LEAD KIT
FDA 510(k)
FDA Class 2
·Neurology
Renovis Tesera SC Stand-alone Anterior Cervical Fusion (ACF) System
FDA 510(k)
FDA Class 2
·Orthopedic
PULSE-GENERATOR, PACEMAKER, IMPLANTABLE
FDA Adverse Event
Malfunction
·RICE CREEK MANUFACTURING·Product code DXY·February 9, 2013
INTEGRATED APD SET W/CASSETTE3 PRONG
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·January 7, 2011
RIATA ST OPTIM ACTIVE FIXATION
FDA Adverse Event
Death
·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·July 23, 2014