BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    *

    MDR report key: 338030 · Received June 7, 2001

    Report

    Report Number
    1418479-2001-00041
    Event Type
    Malfunction
    Date Received
    June 7, 2001
    Date of Event
    March 15, 2001
    Product Code
    KTF
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    26729 * KTF

    Patients

    Seq Age Sex Outcome Treatment
    1