BEUDAMED
    FDA Adverse Event Death Summary report: N

    6000026-1999-00019

    MDR report key: 257389 · Received January 3, 2000

    Report

    Report Number
    6000026-1999-00019
    Event Type
    Death
    Date Received
    January 3, 2000
    Date of Event
    November 21, 1999
    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