BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ANESTAR ANESTHESIA SYSTEM

    MDR report key: 3091545 · Received April 30, 2013

    Report

    Report Number
    2221819-2013-00783
    Event Type
    Malfunction
    Date Received
    April 30, 2013
    Date of Event
    November 1, 2012
    Report Date
    April 30, 2013
    Manufacturer
    MINDRAY DS USA, INC.
    Product Code
    BSZ
    PMA / PMN Number
    001988
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    MINDRAY SERVICE REPRESENTATIVE REPLACED THE O2 SENSOR, CALIBRATED THE TESTED THE UNIT.

    Description of Event or Problem · 1

    CUSTOMER REPORTED THE ANESTAR ANESTHESIA SYSTEM DISPLAYED LOW O2 READINGS. NO PATIENT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    187234 ANESTAR ANESTHESIA SYSTEM ANESTHESIA DELIVERY SYSTEM BSZ MINDRAY DS USA, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1