BEUDAMED
    FDA Adverse Event Other Summary report: N

    NO POWER

    MDR report key: 1342463 · Received March 5, 2009

    Report

    Report Number
    1019632-2009-00003
    Event Type
    Other
    Date Received
    March 5, 2009
    Report Date
    March 5, 2009
    Manufacturer
    ANSELL MEDICAL SDN
    Product Code
    KGO
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US

    Narratives

    Description of Event or Problem · 1

    WHILE WORKING WITH A PT, EYES WERE CONTAMINATED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NO POWER SURGICAL GLOVES KGO ANSELL MEDICAL SDN 0801405504

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK Other