BEUDAMED
    FDA Adverse Event Other Summary report: N

    9610617-2008-00015

    MDR report key: 1175324 · Received July 3, 2008

    Report

    Report Number
    9610617-2008-00015
    Event Type
    Other
    Date Received
    July 3, 2008
    Product Code
    FPK
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    EQUIMAT WAS RECENTLY RELEASED FOR EVAL, BUT HAS NOT BEEN RETURNED YET.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FPK

    Patients

    Seq Age Sex Outcome Treatment
    1