BEUDAMED
    FDA Adverse Event Injury Summary report: N

    1920664-2007-00488

    MDR report key: 845450 · Received April 26, 2007

    Report

    Report Number
    1920664-2007-00488
    Event Type
    Injury
    Date Received
    April 26, 2007
    Product Code
    HQL
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1