BEUDAMED
    FDA Adverse Event Summary report: N

    *

    MDR report key: 282267 · Received June 13, 2000

    Report

    Report Number
    9610617-2000-00009
    Date Received
    June 13, 2000
    Date of Event
    May 18, 2000
    Manufacturer
    KARL STORZ GMBH & CO.
    Product Code
    FEQ
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * * FEQ KARL STORZ GMBH & CO. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 *