BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CODMAN DISPOSABLE VEIN STRIPPER

    MDR report key: 488887 · Received October 1, 2003

    Report

    Report Number
    1226348-2003-00216
    Event Type
    Injury
    Date Received
    October 1, 2003
    Date of Event
    August 27, 2003
    Manufacturer
    CODMAN & SHURTLEFF, INC.
    Product Code
    GAJ
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CODMAN DISPOSABLE VEIN STRIPPER STRIPPER, VEIN, DISPOSABLE GAJ CODMAN & SHURTLEFF, INC. NA FV495

    Patients

    Seq Age Sex Outcome Treatment
    1