BEUDAMED
    FDA Adverse Event Other Summary report: N

    *

    MDR report key: 572945 · Received February 14, 2005

    Report

    Report Number
    9680515-2005-00001
    Event Type
    Other
    Date Received
    February 14, 2005
    Manufacturer
    *
    Product Code
    DWS
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * * DWS * * *

    Patients

    Seq Age Sex Outcome Treatment
    1 *