BEUDAMED
    4 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PULSE GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS INC·Product code MUZ·April 10, 2013

    CODMAN DISP PERFORATOR

    FDA Adverse Event
    Injury ·CODMAN AND SHURTLEFF, INC.·Product code HBF·April 4, 2011

    RIATA ST OPTIM ACTIVE FIXATION LEAD

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 27, 2008

    PROFORMA HF 4.5 CANN CURVED 5/BX

    FDA Adverse Event
    Malfunction ·CONMED UTICA·Product code DSA·August 26, 2021