BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2110898-1996-00002

    MDR report key: 45090 · Received October 1, 1996

    Report

    Report Number
    2110898-1996-00002
    Event Type
    Injury
    Date Received
    October 1, 1996
    Date of Event
    June 21, 1996
    Product Code
    HRX
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HRX 83000

    Patients

    Seq Age Sex Outcome Treatment
    1 *