BEUDAMED
    FDA Adverse Event Other Summary report: N

    1047439-2002-00010

    MDR report key: 383883 · Received March 11, 2002

    Report

    Report Number
    1047439-2002-00010
    Event Type
    Other
    Date Received
    March 11, 2002
    Date of Event
    January 11, 2002
    Product Code
    HOZ
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1