BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    1920664-1997-00200

    MDR report key: 84242 · Received April 14, 1997

    Report

    Report Number
    1920664-1997-00200
    Event Type
    Malfunction
    Date Received
    April 14, 1997
    Date of Event
    March 17, 1997
    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