BEUDAMED
    FDA Adverse Event Injury Summary report: N

    THINLINE 2 EZ

    MDR report key: 1452212 · Received August 7, 2009

    Report

    Report Number
    2124215-2009-12392
    Event Type
    Injury
    Date Received
    August 7, 2009
    Date of Event
    June 4, 2009
    Report Date
    August 7, 2009
    Manufacturer
    CPI - DEL CARIBE
    Product Code
    DTB
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 THINLINE 2 EZ IMPLANTABLE LEAD DTB CPI - DEL CARIBE 438-35S-58 NA