BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PILLING CORONARY SCISSORS

    MDR report key: 1033156 · Received April 23, 2008

    Report

    Report Number
    1044475-2008-00010
    Event Type
    Malfunction
    Date Received
    April 23, 2008
    Report Date
    March 28, 2008
    Manufacturer
    TELEFLEX MEDICAL
    Product Code
    LRW
    PMA / PMN Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FR
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    THE DEVICE HAS BEEN REQUESTED FOR INVESTIGATION, BUT HAS NOT BEEN REC'D YET. SHOULD THE DEVICE BECOME AVAILABLE, A DETAILED REVIEW OF THE DEVICE WILL BE PERFORMED.

    Description of Event or Problem · 1

    COMPLAINT REPORTED: "THE SCISSORS BROKE WHEN THEY WERE BEING USED ON PT." NO REPORTED INJURIES. NO FURTHER INFO OBTAINED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PILLING CORONARY SCISSORS CORONARY SCISSORS LRW TELEFLEX MEDICAL MM6

    Patients

    Seq Age Sex Outcome Treatment
    1