BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2132280-2001-00003

    MDR report key: 332800 · Received May 15, 2001

    Report

    Report Number
    2132280-2001-00003
    Event Type
    Injury
    Date Received
    May 15, 2001
    Date of Event
    April 23, 2001
    Product Code
    ---
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    22866 ---

    Patients

    Seq Age Sex Outcome Treatment
    1