BEUDAMED
    22 results · 37ms · Sources: EU EUDAMED, US FDA

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    PhenoMATRIX

    FDA 510(k)
    FDA Class 2 ·Microbiology

    iFill

    FDA UDI
    Control Devices, LLC·G2982515110·Oxygen VIPR, IFILL, 0-10 L/min

    Insignia

    FDA UDI
    ALPHATEC SPINE, INC.·00190376475332·Trial Drill Guide, 11mm

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946099534·Defibrillator ,MAIN ASSY, X SERIES MONITOR/DEFI...

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B167312515110·

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946062552·X SERIES MONITOR/DEFIBRILLATOR 12 LEAD/W INTERP...

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946019754·Defibrillator ,MAIN ASSY, X SERIES MONITOR/DEFI...

    TALOS® HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B167322515110·

    Reprocessed Endoscopic Trocars and Sleeves

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ROSA Spine

    FDA 510(k)
    FDA Class 2 ·Neurology

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code NAY·January 11, 2019

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code NAY·January 11, 2019

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code OLO·March 13, 2019

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·September 3, 2014

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·September 16, 2011

    FORCE FX

    FDA Adverse Event
    Malfunction ·COVIDIEN FORMERLY VALLEY LAB·Product code GEI·July 9, 2013

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code OLO·April 10, 2019

    ROSA ONE

    FDA Adverse Event
    Injury ·MEDTECH SA·Product code OLO·February 22, 2019

    ROSA ONE

    FDA Adverse Event
    Injury ·MEDTECH SA·Product code OLO·March 11, 2019

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code NAY·April 3, 2019