BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    *

    MDR report key: 204720 · Received December 31, 1998

    Report

    Report Number
    9612030-1998-00011
    Event Type
    Malfunction
    Date Received
    December 31, 1998
    Date of Event
    December 3, 1998
    Product Code
    LRQ
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1