BEUDAMED
    4 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SPINAL VERTEBRAL BODY REPLACEMENT DEVICE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MQP·April 25, 2016

    FUSION OMNI-TOME

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL·Product code KNS·February 28, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 5, 2011

    CAPSURE VDD 2

    FDA Adverse Event
    Injury ·MPRI·Product code DXY·August 8, 2014