BEUDAMED
    FDA Adverse Event Summary report: N

    1222081-2006-00017

    MDR report key: 697554 · Received March 28, 2006

    Report

    Report Number
    1222081-2006-00017
    Date Received
    March 28, 2006
    Date of Event
    February 17, 2005
    Product Code
    HTT
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1