BEUDAMED
    FDA Registration Active 🇩🇪 Germany

    ARTROMOT®-E2 Compact

    Reg #: 3007740591 · FEI: 3007740591 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    12
    Establishment Types
    3
    Classifications
    1

    Registration Details

    Registration Name
    DJO Global / Germany
    Registration Number
    3007740591
    FEI Number
    3007740591
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    ORMED GmbH, Boetzinger Strasse 90
    City
    Freiburg Baden-Wurttemberg
    Country
    DE

    Owner / Operator

    Firm Name
    DJO, LLC
    Operator Number
    9015378
    Address
    5919 Sea Otter Place, Suite 200
    City
    Carlsbad
    State
    CA
    Postal Code
    92010
    Country
    US
    Correspondent
    Dave Hunter

    Products

    Device Name Product Code
    Exerciser, Powered BXB

    Proprietary Names

    ARTROMOT®-E2 Compact OptiFlex®-S OptiFlex®-K1 Standard OptiFlex®-K1 Comfort Chip OptiFlex®-K1 Classic ARTROMOT®-E2 ARTROMOT®-SP3 Comfort Chip ARTROMOT® ACTIVE-K ARTROMOT®-SP3 Comfort ARTROMOT®-SP3 Standard ARTROMOT®-S4 ARTROMOT®-SP3 Standard Chip

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility Export Device to the United States But Perform No Other Operation on Device Manufacture Medical Device