BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LD304 MATERNITY BED

    MDR report key: 1964506 · Received December 22, 2010

    Report

    Report Number
    1831750-2010-05145
    Event Type
    Malfunction
    Date Received
    December 22, 2010
    Date of Event
    November 27, 2010
    Report Date
    November 27, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    HDD
    PMA / PMN Number
    K950889
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    CALF SUPPORTS.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE CALF SUPPORTS NOT HOLDING WITH PATIENT WEIGHT. THERE WAS PATIENT INVOLVEMENT; HOWEVER, NO ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LD304 MATERNITY BED LABOR AND DELIVERY BED HDD STRYKER CORP., MEDICAL DIV. 4701 NA

    Patients

    Seq Age Sex Outcome Treatment
    1