BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    *

    MDR report key: 2291306 · Received September 29, 2011

    Report

    Report Number
    2291306
    Event Type
    Malfunction
    Date Received
    September 29, 2011
    Date of Event
    September 1, 2011
    Report Date
    September 29, 2011
    Manufacturer
    KCI, INC.
    Product Code
    OMP
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    OH, US
    Reporter Occupation
    RISK MANAGER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * NEGATIVE PRESSURE WOUND THERAPY SYSTEM OMP KCI, INC. * 50586196

    Patients

    Seq Age Sex Outcome Treatment
    1 *