BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Versacut Tissue Morcellator

    Reg #: 1720381 · FEI: 1720381 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    4
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    LUMENIS, INC.
    Registration Number
    1720381
    FEI Number
    1720381
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    1870 S Milestone Dr
    City
    SALT LAKE CITY
    State
    UT
    ZIP
    84104
    Country
    US

    Owner / Operator

    Firm Name
    Lumenis Be LTD
    Operator Number
    9017014
    Address
    9 Hakidma St., POB 426, Yokneam Industrial Park
    City
    Yokneam
    State
    IL-NOTA
    Postal Code
    2069236
    Country
    IL

    Products

    Device Name Product Code
    Laparoscope, General & Plastic Surgery GCJ

    Proprietary Names

    Versacut Tissue Morcellator VersaCut Blade Set Sterilization Tray VersaCut Hand Piece

    Establishment Types

    Manufacture Device in the United States for Export Only