BEUDAMED
    FDA Adverse Event Other Summary report: N

    NICOLET ELITE WATERPOOF 2MHZ DOPPLER PROBE

    MDR report key: 375152 · Received January 31, 2002

    Report

    Report Number
    1718469-2002-00001
    Event Type
    Other
    Date Received
    January 31, 2002
    Date of Event
    January 8, 2002
    Report Date
    January 22, 2002
    Manufacturer
    NICOLET VASCULAR
    Product Code
    HEK
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    CUSTOMER STATED THAT PROBE WAS RECEIVED WITH WHAT APPEARED TO BE BLOOD ON THE FACE OF THE PROBE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NICOLET ELITE WATERPOOF 2MHZ DOPPLER PROBE OB DOPPLER PROBE HEK NICOLET VASCULAR X1-L006 *

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other