BEUDAMED
    FDA Adverse Event Summary report: N

    UNK

    MDR report key: 371396 · Received January 7, 2002

    Report

    Report Number
    9613278-2001-00017
    Date Received
    January 7, 2002
    Report Date
    April 9, 2001
    Manufacturer
    BIONX IMPLANTS, LTD.
    Product Code
    ---
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    UNK

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 UNK UNK --- BIONX IMPLANTS, LTD. UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other