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

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    Filters FDA Adverse Event ×

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·RICE CREEK MFG·Product code LWP·February 9, 2013

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·January 10, 2011

    ASCENDRA 3 DELIVERY SYSTEM, 23MM

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code NPT·July 23, 2014

    THERMA CARE

    FDA Adverse Event
    Injury ·PROCTER & GAMBLE PAPER PRODUCT CO·Product code IMD·March 6, 2002