BEUDAMED
    6 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    TORNIER AEQUALIS REVERSE SHOLDER PROSTHESIS

    FDA Adverse Event
    Malfunction ·TORNIER INC.·Product code HSD·June 18, 2009

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HRS·July 25, 2018

    MED SYSTEMS ELECTRO FLO 5000 PERCUSSOR, 30 POWER/FREQUENCY SETTINGS AN

    FDA Adverse Event
    Injury ·MED SYSTEM, INC.·Product code BYI·September 21, 2018

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 3, 2013

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·March 28, 2011

    ASCENSIA BREEZE (US)

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·April 15, 2008