BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LD304 MATERNITY BED

    MDR report key: 1945262 · Received December 10, 2010

    Report

    Report Number
    1831750-2010-04714
    Event Type
    Malfunction
    Date Received
    December 10, 2010
    Date of Event
    November 12, 2010
    Report Date
    November 12, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV
    Product Code
    HDD
    PMA / PMN Number
    K950889
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OK, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SVC REPORT THAT THE PT LEFT SIDERAIL PANEL IS CRACKED. THERE WAS NO PT INVOLVEMENT; HOWEVER ADVERSE CONSEQUENCES ARE UNK.

    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