BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2133615-2003-00001

    MDR report key: 455886 · Received April 25, 2003

    Report

    Report Number
    2133615-2003-00001
    Event Type
    Injury
    Date Received
    April 25, 2003
    Date of Event
    March 27, 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