BEUDAMED
    FDA Adverse Event Injury Summary report: N

    NONE

    MDR report key: 2212446 · Received September 10, 2008

    Report

    Report Number
    2249697-2008-00259
    Event Type
    Injury
    Date Received
    September 10, 2008
    Product Code
    JWH
    PMA / PMN Number
    UNK
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    DEVICE NOT RETURNED. NO EVAL WILL BE PERFORMED. IF DEVICE BECOMES AVAILABLE WITH ADDITIONAL INFO A SUPPLEMENTAL REPORT WILL BE ISSUED.

    Description of Event or Problem · 1

    SERIOUS INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NONE JWH

    Patients

    Seq Age Sex Outcome Treatment
    1