BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Monicor-Rofes Biofeedback Device

    Reg #: 3025460482 · FEI: 3025460482 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    2
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Monicor USA Corporation
    Registration Number
    3025460482
    FEI Number
    3025460482
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    5130 S Fort Apache Rd., Suite 215-375
    City
    Las Vegas
    State
    NV
    ZIP
    89148
    Country
    US

    Owner / Operator

    Firm Name
    Monicor USA Corporation
    Operator Number
    10086832
    Address
    5130 S Fort Apache Rd., Suite 215-375
    City
    Las Vegas
    State
    NV
    Postal Code
    89148
    Country
    US
    Correspondent
    Robert Wagner

    Products

    Device Name Product Code
    Device, Biofeedback HCC

    Proprietary Names

    Monicor-Rofes Biofeedback Device Monicor-Rofes Biofeedback Device Pro

    Establishment Types

    Manufacture Medical Device