BEUDAMED
    9 results · 29ms · 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

    FORTIFY DR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL INC., CARDIAC RHYTHM MANAGEMENT D·Product code LWS·January 13, 2014

    TERUMO CDI 500 BLOOD PARAMETER MONITOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·October 13, 2010

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·December 19, 2012

    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