BEUDAMED
    FDA Adverse Event Death Summary report: N

    2031527-2012-00113

    MDR report key: 2859304 · Received December 5, 2012

    Report

    Report Number
    2031527-2012-00113
    Event Type
    Death
    Date Received
    December 5, 2012
    Date of Event
    August 14, 2012
    Report Date
    August 14, 2012
    Manufacturer
    ENDOLOGIX, INC.
    PMA / PMN Number
    P040002
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    PHYSICIAN
    Health Professional
    Yes

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Female Death