BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CREATIVE MEDICAL TECHNOLOGIES, INC

    MDR report key: 310682 · Received December 21, 2000

    Report

    Report Number
    310682
    Event Type
    Injury
    Date Received
    December 21, 2000
    Date of Event
    October 3, 2000
    Report Date
    October 17, 2000
    Manufacturer
    CREATIVE MEDICAL TECHNOLOGIES INC
    Product Code
    CAW
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    NC, US
    Reporter Occupation
    NURSE

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CREATIVE MEDICAL TECHNOLOGIES, INC OXYGEN CONCENTRATOR CAW CREATIVE MEDICAL TECHNOLOGIES INC VA 950673 *

    Patients

    Seq Age Sex Outcome Treatment
    1 86 YR Hospitalization