BEUDAMED
    FDA Adverse Event Other Summary report: N

    CLARUS MEDICAL LASE

    MDR report key: 311562 · Received December 29, 2000

    Report

    Report Number
    2183911-2000-00003
    Event Type
    Other
    Date Received
    December 29, 2000
    Report Date
    December 28, 2000
    Manufacturer
    CLARUS MEDICAL, LLC
    Product Code
    GEX
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    OTHER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CLARUS MEDICAL LASE ENDOSCOPIC DISECTOMY DEVICE GEX CLARUS MEDICAL, LLC 1100 - UNKNOWN UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other