BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PROSENSE CRYOABLATION SYSTEM

    MDR report key: 17909759 · Received October 10, 2023

    Report

    Report Number
    3008797959-2023-00003
    Event Type
    Injury
    Date Received
    October 10, 2023
    Date of Event
    November 29, 2021
    Report Date
    October 11, 2023
    Manufacturer
    ICECURE MEDICAL LTD.
    Product Code
    GEH
    PMA / PMN Number
    K183213
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IS
    Reporter Occupation
    003

    Narratives

    Additional Manufacturer Narrative · 0

    AS DETAILED ABOVE.

    Description of Event or Problem · 0

    CRYOPROBE BENDING DUE TO USE ERROR WAS REPORTED, WITH NO SERIOUS INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2164384 PROSENSE CRYOABLATION SYSTEM PROSENSE CRYOABLATION SYSTEM GEH ICECURE MEDICAL LTD. FAS3100000,FAP7800000

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown Other