BEUDAMED
    4 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ZEPHYR XL DR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWP·January 15, 2014

    TRIDENT HEMI CUP

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK·Product code JDI·November 29, 2010

    LIFESHIELD PRIMARY PLUMSET, CLAVE, PORT CLAVE Y SITE

    FDA Adverse Event
    Malfunction ·HOSPIRA·Product code FPA·October 31, 2012

    BD BACTEC FX, INSTRUMENT TOP, PACKAGED

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code MDB·February 22, 2021