BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2110898-1997-00013

    MDR report key: 94899 · Received May 28, 1997

    Report

    Report Number
    2110898-1997-00013
    Event Type
    Injury
    Date Received
    May 28, 1997
    Date of Event
    April 3, 1997
    Product Code
    HRX
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1