BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SLINGS, CLIP

    MDR report key: 3823636 · Received April 7, 2014

    Report

    Report Number
    3007420694-2014-00040
    Event Type
    Malfunction
    Date Received
    April 7, 2014
    Date of Event
    December 20, 2013
    Report Date
    March 7, 2014
    Manufacturer
    ARJOHUNTLEIGH POLSKA SP. ZO.O.
    Product Code
    IKX
    Product Problem
    Yes
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4).

    Description of Event or Problem · 1

    (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    207678 SLINGS, CLIP IKX ARJOHUNTLEIGH POLSKA SP. ZO.O.

    Patients

    Seq Age Sex Outcome Treatment
    1 Other