9 results
·
19ms
·
Sources: EU EUDAMED, US FDA
PROTECTOR (SURGICAL INSTRUMENT)
FDA 510(k)
FDA Class 2
·General Hospital
Epicage Interbody Fusion System
FDA UDI
ALPHATEC SPINE, INC.·00840967190761·Oblique Portal – 14mm
FORZA
FDA UDI
Orthofix US LLC·18257200077465·9W X 27L X 0° X 14H CURVED TRIAL
Advanced Intelligent Volumetric Ultrasound System, Model AiVUS 1000
FDA 510(k)
FDA Class 2
·Radiology
FLUID ADMINISTRATION SETS, 15 MICRON
FDA 510(k)
FDA Class 2
·General Hospital
ULTRACISION HARMONIC ACE
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·April 29, 2016
CURRENT PLUS DR, DF-4 CONNECTOR
FDA Adverse Event
Injury
·ST. JUDE MEDICAL INC., CRMD·Product code LWS·January 13, 2014
ACCU-CHEK ® AVIVA TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·November 3, 2010
ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·CORDIS NEUROVASCULAR, INC.·Product code NJE·December 29, 2012