BEUDAMED
    7 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    LUMBAR CATHETER ACCESSORY KIT (LCAK)

    FDA Adverse Event
    Malfunction ·INTEGRA NEUROSCIENCES IMPLANTS S.A.·Product code JXG·April 29, 2004

    MBT CEM KEEL TIB TRAY SZ4

    FDA Adverse Event
    Injury ·DEPUY-CORK, A DIVISION OF DEPUY ORTHOPAEDICS·Product code NJL·November 19, 2008

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·September 8, 2011

    ENERGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 22, 2013

    SPACEMAKER

    FDA Adverse Event
    Malfunction ·US SURGICAL PUERTO RICO·Product code GCJ·July 13, 2023

    DVR PEG SMOOTH 2.0MM X 26MM

    FDA Adverse Event
    Malfunction ·BIOMET TRAUMA·Product code LXT·July 7, 2017

    DVR PEG SMOOTH 2.0MM X 18MM

    FDA Adverse Event
    Malfunction ·BIOMET TRAUMA·Product code LXT·July 7, 2017