BEUDAMED
    9 results · 46ms · Sources: EU EUDAMED, US FDA

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    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF·Product code LKK·July 25, 2023

    CODMAN 3000

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF·Product code LKK·July 28, 2023

    CODMAN 3000

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF·Product code LKK·July 20, 2023

    CODMAN

    FDA Adverse Event
    Death ·CODMAN & SHURTLEFF·Product code LKK·July 18, 2023

    DEPUY/CMW 2G

    FDA Adverse Event
    Injury ·DEPUY CMW - 9610921·Product code LOD·December 27, 2019

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 30, 2014

    PRECISION®

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·November 20, 2012

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·September 21, 2010

    PFC SIG RPF CEM FEM SZ 4 RT

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDICS1219655·Product code NJL·September 16, 2014