BEUDAMED
    FDA Adverse Event Summary report: N

    *

    MDR report key: 511160 · Received February 5, 2004

    Report

    Report Number
    1221826-2004-00002
    Date Received
    February 5, 2004
    Date of Event
    January 12, 2004
    Manufacturer
    *
    Product Code
    KQT
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 *