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

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    Filters FDA Adverse Event ×

    CONSULTA

    FDA Adverse Event
    Malfunction ·MEDTRONIC S.A.·Product code LWS·December 14, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 22, 2013

    UNKNOWN_RECONSTRUCTIVE_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·July 9, 2014