BEUDAMED
    FDA Adverse Event Death Summary report: N

    RESUSCITATION ACE

    MDR report key: 378307 · Received February 19, 2002

    Report

    Report Number
    1066658-2002-00001
    Event Type
    Death
    Date Received
    February 19, 2002
    Date of Event
    January 22, 2002
    Report Date
    February 15, 2002
    Manufacturer
    RESUSCITATION ACE, INC.
    Product Code
    CCK
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RESUSCITATION ACE END-TIDAL CO2 DETECTOR/COLORMETRIC CCK RESUSCITATION ACE, INC. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 Death