BEUDAMED
    6 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    FORCEPS CEV405 FENESTRATED 350MM JOHANN [MXI/XOM]

    FDA Adverse Event
    Injury ·XOMED MICROFRANCE MFG·Product code GEI·March 19, 2014

    OMNIGUIDE SURGICAL

    FDA Adverse Event
    Malfunction ·OMNIGUIDE SURGICAL·Product code GEX·June 27, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·November 12, 2010

    PINNACLE MTL INS NEUT40IDX56OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·January 14, 2013

    PIPELINE

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·October 12, 2023

    PIPELINE

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·October 13, 2023