BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9610175-2014-00008

    MDR report key: 3686490 · Received March 18, 2014

    Report

    Report Number
    9610175-2014-00008
    Event Type
    Malfunction
    Date Received
    March 18, 2014
    Date of Event
    February 13, 2014
    Report Date
    February 13, 2014
    Manufacturer
    FRANTZ MEDICAL DEVELOPMENT LTD.
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TU
    Reporter Occupation
    UNKNOWN
    Health Professional
    *

    Patients

    Seq Age Sex Outcome Treatment
    1 77 YR Female