BEUDAMED
    FDA Adverse Event Other Summary report: N

    1220828-2002-00001

    MDR report key: 388322 · Received April 15, 2002

    Report

    Report Number
    1220828-2002-00001
    Event Type
    Other
    Date Received
    April 15, 2002
    Date of Event
    January 14, 2002
    Product Code
    BTM
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1