BEUDAMED
    FDA Adverse Event Summary report: N

    9610617-2001-00032

    MDR report key: 371164 · Received January 10, 2002

    Report

    Report Number
    9610617-2001-00032
    Date Received
    January 10, 2002
    Date of Event
    April 20, 2001
    Product Code
    FBJ
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1