BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    1920664-1997-00052

    MDR report key: 64469 · Received January 17, 1997

    Report

    Report Number
    1920664-1997-00052
    Event Type
    Malfunction
    Date Received
    January 17, 1997
    Date of Event
    December 17, 1996
    Product Code
    HQE
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1