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

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    Filters FDA Adverse Event ×

    ABS 2-0 GR 18 GS-21

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GAM·December 1, 2015

    TELIGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 3, 2014

    LIFEPAK(R) 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·May 31, 2013

    MEDTRONIC EDM LUMBAR CATHETER, CLOSED TIP, BARIUM IMPREGNATED, 80

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code JXG·June 21, 2011