BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    7951000

    MDR report key: 7951000 · Received October 10, 2018

    Report

    Report Number
    7951000
    Event Type
    Malfunction
    Date Received
    October 10, 2018
    Date of Event
    April 5, 2018
    Report Date
    April 9, 2018
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    PA
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    DEVICE DID NOT FUNCTION AS EXPECTED. SUCTION CUPS WERE NOT "GRIPPING".

    Patients

    Seq Age Sex Outcome Treatment
    1 25185 DA