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

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    Filters FDA Adverse Event ×

    PULSE GEN MODEL 102R

    FDA Adverse Event
    Malfunction ·CYBERONICS INC·Product code LYJ·May 8, 2014

    VISIONAIRE LEGION FE

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code KDC·October 23, 2012

    CONING WORKS LLC

    FDA Adverse Event
    Injury ·CONING WORKS, LLC·Product code KCN·August 9, 2010

    BD BACTEC¿ FX, INSTRUMENT TOP, PACKAGED

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code MDB·May 18, 2021