BEUDAMED
    FDA Adverse Event Other Summary report: N

    NONE

    MDR report key: 2138045 · Received October 19, 2007

    Report

    Report Number
    3004475983-2007-00003
    Event Type
    Other
    Date Received
    October 19, 2007
    Product Code
    FDG
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    INTEGRA LIFESCIENCES CORPORATION IS FILING ON BEHALF OF THE INITIAL DISTRIBUTOR (B)(4). CORRESPONDENCE SHOULD BE SENT TO: INTEGRA LIFESCIENCES CORPORATION; (B)(4); ATTN: CORPORATE COMPLAINT COORDINATOR. THE MANUFACTURER HAS BEEN NOTIFIED OF THE REPORTED COMPLAINT.

    Description of Event or Problem · 1

    .

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NONE FDG

    Patients

    Seq Age Sex Outcome Treatment
    1