BEUDAMED
    FDA Adverse Event Injury Summary report: N

    6000026-2001-00008

    MDR report key: 350474 · Received September 7, 2001

    Report

    Report Number
    6000026-2001-00008
    Event Type
    Injury
    Date Received
    September 7, 2001
    Date of Event
    July 26, 2001
    Manufacturer
    MEDTRONIC HEART VALVES, INC.
    Product Code
    LWQ
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    40516 LWQ MEDTRONIC HEART VALVES, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1