BEUDAMED
    FDA Adverse Event Other Summary report: N

    *

    MDR report key: 1311572 · Received November 10, 2008

    Report

    Report Number
    9610617-2008-00026
    Event Type
    Other
    Date Received
    November 10, 2008
    Manufacturer
    KARL STORZ GMBH & CO. KG
    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 KARL STORZ GMBH & CO. KG

    Patients

    Seq Age Sex Outcome Treatment
    1