BEUDAMED
    8 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code MCM·August 23, 2016

    NUCLEUS 22

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

    HFV PATIENT CIRCUIT

    FDA Adverse Event
    Malfunction ·BUNNELL·Product code LSZ·September 14, 2012

    HFV PATIENT CIRCUIT

    FDA Adverse Event
    Malfunction ·BUNNELL·Product code LSZ·September 14, 2012

    HFV PATIENT CIRCUIT

    FDA Adverse Event
    Malfunction ·BUNNELL·Product code LSZ·September 14, 2012

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 30, 2014

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM DE MEXICO S DE RL DE CV·Product code FPO·November 13, 2012

    ALLEGRETTO WAVE

    FDA Adverse Event
    Malfunction ·WAVELIGHT GMBH·Product code LZS·September 15, 2010