BEUDAMED
    FDA Adverse Event Injury Summary report: N

    BIOPRO

    MDR report key: 526006 · Received May 18, 2004

    Report

    Report Number
    1833506-2004-00001
    Event Type
    Injury
    Date Received
    May 18, 2004
    Date of Event
    March 4, 2004
    Report Date
    April 16, 2004
    Manufacturer
    BIOPRO, INC.
    Product Code
    KWD
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WI, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    PATIENT COMPLAINT OF APIN AND THICKNESS OF TOE AND SLIGHTLY LIMITED RANGE OF MOTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BIOPRO TOE MP JOINT KWD BIOPRO, INC. UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 74 YR Required Intervention