BEUDAMED
    5 results · 31ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PECTUS SYSTEM DEFAZIO 13 TI PECTUS BAR

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HRS·February 24, 2020

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·June 19, 2014

    WALLFLEX BILIARY RX FULLY-COVERED STENT SYSTEM, MODEL M00570500,M00570510, M0057

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code FGE·October 28, 2010

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code GEX·December 19, 2012

    PECTUS SYSTEM DEFAZIO 13.5 TI PECTUS BAR

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HRS·February 24, 2020