BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2031527-2012-00108

    MDR report key: 2808143 · Received October 29, 2012

    Report

    Report Number
    2031527-2012-00108
    Event Type
    Malfunction
    Date Received
    October 29, 2012
    Date of Event
    August 2, 2012
    Report Date
    August 2, 2012
    Manufacturer
    ENDOLOGIX, INC.
    PMA / PMN Number
    P040002
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    PHYSICIAN
    Health Professional
    Yes

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown