BEUDAMED
    FDA Adverse Event Injury Summary report: N

    1811755-1998-00060

    MDR report key: 204436 · Received December 29, 1998

    Report

    Report Number
    1811755-1998-00060
    Event Type
    Injury
    Date Received
    December 29, 1998
    Date of Event
    November 11, 1998
    Product Code
    DZH
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1