BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    WIRE,TONSIL,SNARE #7

    MDR report key: 230885 · Received June 17, 1999

    Report

    Report Number
    6000008-1999-00006
    Event Type
    Malfunction
    Date Received
    June 17, 1999
    Date of Event
    February 26, 1999
    Report Date
    June 16, 1999
    Manufacturer
    BAUER & HASELBARTH GMBH
    Product Code
    KBZ
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    RISK MANAGER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 WIRE,TONSIL,SNARE #7 INSTRUMENT KBZ BAUER & HASELBARTH GMBH MO2010-007 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other