BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2249697-2008-00223

    MDR report key: 1110704 · Received August 4, 2008

    Report

    Report Number
    2249697-2008-00223
    Event Type
    Injury
    Date Received
    August 4, 2008
    Product Code
    KWY
    PMA / PMN Number
    K983382
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Narratives

    Additional Manufacturer Narrative · 1

    DEVICE IS NOT AVAILABLE FOR EVAL. NO EVAL WILL BE PERFORMED. ADD'L INFO HAS BEEN REQUESTED AND IF RECEIVED WILL BE PROVIDED ON A SUPPLEMENTAL REPORT.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1