BEUDAMED
    FDA Registration Active 🇺🇸 United States

    NexGen 900 Series

    Reg #: 3004989804 · FEI: 3004989804 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    4
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    MEDICATECH USA
    Registration Number
    3004989804
    FEI Number
    3004989804
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1245 N Patt St
    City
    Anaheim
    State
    CA
    ZIP
    92801
    Country
    US

    Owner / Operator

    Firm Name
    Medicatech USA
    Operator Number
    9073041
    Address
    1245 N Patt Street
    City
    Anaheim
    State
    CA
    Postal Code
    92801
    Country
    US
    Correspondent
    George Makar

    Products

    Device Name Product Code
    Generator, High-Voltage, X-Ray, Diagnostic IZO

    Proprietary Names

    NexGen 900 Series NexGen 940 Series NexGen 960 Series NexGen 950 Series

    Establishment Types

    Repack or Relabel Medical Device