BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    1920664-2003-00239

    MDR report key: 458318 · Received May 2, 2003

    Report

    Report Number
    1920664-2003-00239
    Event Type
    Malfunction
    Date Received
    May 2, 2003
    Date of Event
    February 26, 2003
    Product Code
    ---
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1