BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    JAKO LARYNGEAL PROBE, ANGLED

    MDR report key: 275840 · Received April 28, 2000

    Report

    Report Number
    1423507-2000-00116
    Event Type
    Malfunction
    Date Received
    April 28, 2000
    Date of Event
    February 11, 2000
    Report Date
    April 28, 2000
    Product Code
    KAK
    Product Problem
    Yes
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 JAKO LARYNGEAL PROBE, ANGLED INSTRUMENT KAK BE2847 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 Other