BEUDAMED
    FDA Adverse Event Death Summary report: N

    *

    MDR report key: 1005270 · Received February 29, 2008

    Report

    Report Number
    1722684-2008-00002
    Event Type
    Death
    Date Received
    February 29, 2008
    Manufacturer
    CLINICAL INNOVATIONS, LLC
    Product Code
    HGS
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Narratives

    Additional Manufacturer Narrative · 1

    WE HAVE CONTACTED THE HOSPITAL SEVERAL TIMES, BUT AS OF THE DATE OF THIS FILING, HAVE NOT RECEIVED ANY FURTHER INFO.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * * HGS CLINICAL INNOVATIONS, LLC * *

    Patients

    Seq Age Sex Outcome Treatment
    1 0 DAY