BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    A5 ANESTHESIA SYSTEM

    MDR report key: 3091596 · Received April 30, 2013

    Report

    Report Number
    2221819-2013-00706
    Event Type
    Malfunction
    Date Received
    April 30, 2013
    Date of Event
    November 28, 2012
    Report Date
    April 30, 2013
    Manufacturer
    MINDRAY DS USA, INC.
    Product Code
    BSZ
    PMA / PMN Number
    123211
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    MINDRAY SERVICE REPRESENTATIVES TIGHTENED THE CANISTER WATER TRAP AND RESOLVED THE ISSUE. PERFORMED ALL FUNCTIONAL AND SAFETY CHECKS AND UNIT WAS RETURNED TO SERVICE.

    Description of Event or Problem · 1

    CUSTOMER REPORTED THE A5 ANESTHESIA SYSTEM HAD A SYSTEM LEAK WHICH MAY HAVE AFFECTED ANESTHESIA MONITORING. NO PATIENT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    186577 A5 ANESTHESIA SYSTEM ANESTHESIA DELIVERY SYSTEM BSZ MINDRAY DS USA, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1