BEUDAMED
    FDA Adverse Event Summary report: N

    2023366-1996-90001

    MDR report key: 63627 · Received January 15, 1997

    Report

    Report Number
    2023366-1996-90001
    Date Received
    January 15, 1997
    Date of Event
    October 29, 1996
    Product Code
    HQL
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1