BEUDAMED
    FDA Adverse Event Other Summary report: N

    *

    MDR report key: 965784 · Received September 21, 2005

    Report

    Report Number
    8010877-2005-00004
    Event Type
    Other
    Date Received
    September 21, 2005
    Manufacturer
    KOSCHER & WUERTZ GMBH
    Product Code
    ---
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    AN INVESTIGATION HAS BEEN INITIATED BASED ON THE REPORTED INFO.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * --- KOSCHER & WUERTZ GMBH

    Patients

    Seq Age Sex Outcome Treatment
    1