BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HRS·November 16, 2015

    4.0MM CANCELLOUS BONE SCREW PARTIALLY THREADED/45MM

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HWC·December 9, 2015

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 7, 2014

    EON IPG

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·October 20, 2010

    RESTORE ULTRA

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LGW·December 21, 2012

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·September 1, 2016

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·December 4, 2015

    4.0MM CANCELLOUS BONE SCREW FULLY THREADED/45MM

    FDA Adverse Event
    Injury ·SYNTHES GRENCHEN·Product code HWC·December 18, 2015