BEUDAMED
    FDA Adverse Event Injury Summary report: N

    1418957-1997-00005

    MDR report key: 101530 · Received June 13, 1997

    Report

    Report Number
    1418957-1997-00005
    Event Type
    Injury
    Date Received
    June 13, 1997
    Date of Event
    September 19, 1996
    Product Code
    IZO
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 IZO 55761G-2 0237-1293-001

    Patients

    Seq Age Sex Outcome Treatment
    1 *