BEUDAMED
    FDA Adverse Event Injury Summary report: N

    1825034-2000-00048

    MDR report key: 284381 · Received June 30, 2000

    Report

    Report Number
    1825034-2000-00048
    Event Type
    Injury
    Date Received
    June 30, 2000
    Date of Event
    May 12, 2000
    Product Code
    KWB
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 KWB

    Patients

    Seq Age Sex Outcome Treatment
    1