9 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SPQ(TM) ANTIBODY REAGENT SET II FOR AAT
FDA 510(k)
FDA Class 2
·Immunology
FORZA
FDA UDI
Orthofix US LLC·18257200078066·ROTATING CUTTER - 15MM
EMINENT SPINE BUTTRESS (FANG) PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ATLAS Plating System
FDA 510(k)
FDA Class 2
·Orthopedic
OT ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·November 3, 2010
FORTIFY VR, DF4 CONNECTOR
FDA Adverse Event
Injury
·ST. JUDE MEDICAL INC., CARDIAC RHYTHM MANAGEMENT D·Product code LWS·January 13, 2014
WALLFLEX¿ ESOPHAGEAL
FDA Adverse Event
Death
·BOSTON SCIENTIFIC - GALWAY·Product code ESW·December 30, 2012
Axiom Artis systems. C-arm angiographic x-ray system x-ray, angiographic system.
FDA Enforcement
Class II
·Terminated·Siemens Medical Solutions USA, Inc·September 4, 2013
AXIOM Sireskop SD Model numbers 8890415 and 8890407. The product is intended for use as radiographic and fluoroscopic imaging device.
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code MQB·January 8, 2009