BEUDAMED
    FDA Registration Active 🇨🇦 Canada

    Scope Rhino Fiberoptic

    Reg #: 3023102955 · FEI: 3023102955 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    CHG-MERIDIAN CANADA LTD
    Registration Number
    3023102955
    FEI Number
    3023102955
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1 Robert Speck Parkway, Suite No. 960
    City
    Mississauga Ontario
    Country
    CA

    Regulatory Submissions

    510(k) Number
    K011869

    Owner / Operator

    Firm Name
    CHG-MERIDIAN CANADA LTD
    Operator Number
    10085392
    Address
    1 Robert Speck Parkway, Suite No. 960
    City
    Mississauga
    State
    Ontario
    Postal Code
    L4Z 2G5
    Country
    CA
    Correspondent
    Ken Berger

    US Agent

    Business Name
    CHG-MERIDIAN USA Corp.
    Contact Name
    Ken Berger
    Address
    21800 Oxnard Street, #400
    City
    Woodland Hills
    State
    CA
    ZIP
    91367
    Country
    US
    Email
    [email protected]
    Phone
    818 7021800

    Products

    Device Name Product Code
    Nasopharyngoscope (Flexible Or Rigid) EOB

    Proprietary Names

    Scope Rhino Fiberoptic

    Establishment Types

    Export Device to the United States But Perform No Other Operation on Device