BEUDAMED
    16 results · 27ms · Sources: EU EUDAMED, US FDA

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    EXPEDIUM Spine System/Synapse System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16741424600·

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1674142460060·

    Luer Capillary

    FDA UDI
    Siemens Healthcare Diagnostics Inc.·00630414482361·Luer Capillary (pack of 20) an in vitro diagnos...

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X1424600·14mm H x 24mm W x 60mm L x 0 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X142460120·14mm H x 24mm W x 60mm L x 12 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L142460120·14mm H x 24mm W x 60mm L XLIF Trial 12 degree L...

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X14246080·14mm H x 24mm W x 60mm L x 8 degrees XLIF

    AMBIT INTRODUCER, AMBIT NEEDLE, AMBIT SHEATH

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    TI - SCREW ANCHOR SP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LIFEPAK(R) 15 MONITOR/DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·August 8, 2016

    LIFEPAK(R) 1000 DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·July 10, 2015

    LIFEPAK(R) 15 MONITOR/DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·December 23, 2014

    RESERVOIR 1.8ML

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·October 5, 2014

    HOY-STATURE

    FDA Adverse Event
    Injury ·APEX HEALTHCARE MFG INC·Product code FNG·March 12, 2013

    DOW CORNING SILASTIC MSI MAMMARY IMPLANT

    FDA Adverse Event
    Injury ·DOW CORNING WRIGHT·Product code FTR·June 22, 2011