BEUDAMED
    FDA Adverse Event Other Summary report: N

    NONE

    MDR report key: 2137894 · Received October 17, 2007

    Report

    Report Number
    8010877-2007-00005
    Event Type
    Other
    Date Received
    October 17, 2007
    Product Code
    GEN
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    INTEGRA LIFESCIENCES CORP IS FILING ON BEHALF OF THE INITIAL DISTRIBUTOR J. JAMNER SURGICAL INSTRUMENTS. CORRESPONDENCE SHOULD BE SENT TO: INTEGRA LIFESCIENCES CORP; (B)(4). ATTN: CORPORATE COMPLAINT COORDINATOR. THE MFR 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 GEN 0444222

    Patients

    Seq Age Sex Outcome Treatment
    1