BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2021710-2001-00147

    MDR report key: 359928 · Received November 6, 2001

    Report

    Report Number
    2021710-2001-00147
    Event Type
    Malfunction
    Date Received
    November 6, 2001
    Date of Event
    February 14, 2001
    Product Code
    MNJ
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    49508 MNJ

    Patients

    Seq Age Sex Outcome Treatment
    1