BEUDAMED
    9 results · 16ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    NUCLEUS 22

    FDA Adverse Event
    Injury ·COCHLEAR LIMITED·Product code MCM·May 18, 2025

    SYNCHROMED

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·September 9, 2010

    RESTYLANE, RESTYLANE

    FDA Adverse Event
    Injury ·Q-MED·Product code LMH·June 11, 2013

    RESTYLANE INJECTABLE GEL

    FDA Adverse Event
    Injury ·Q-MED AB·Product code LMH·August 26, 2011

    RESTYLANE, RESTYLANE

    FDA Adverse Event
    Injury ·Q-MED·Product code LMH·July 11, 2013

    RESTYLANE PERLANE

    FDA Adverse Event
    Injury ·GALDERMA Q-MED·Product code LMH·April 24, 2015

    RESTYLANE, RESTYLANE

    FDA Adverse Event
    Injury ·Q-MED·Product code LMH·February 14, 2014

    RESTYLANE, RESTYLANE

    FDA Adverse Event
    Injury ·Q-MED·Product code LMH·February 21, 2014

    HEARTWARE VENTRICULAR ASSIST SYSTEM - PUMP

    FDA Adverse Event
    Injury ·HEARTWARE, INC.·Product code DSQ·October 24, 2024