BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PAIN CARE 3000

    MDR report key: 2142371 · Received June 20, 2011

    Report

    Report Number
    2028253-2011-00026
    Event Type
    Injury
    Date Received
    June 20, 2011
    Date of Event
    September 16, 2003
    Report Date
    June 17, 2011
    Manufacturer
    BREG, INC
    Product Code
    MEB
    PMA / PMN Number
    K002073
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PT HAD SURGERY. ALLEGES CHONDROLYSIS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PAIN CARE 3000 88 FRN MEB BREG, INC 10314 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 Other| S