BEUDAMED
    FDA Registration Active 🇨🇦 Canada

    CHG-MERIDIAN CANADA LTD

    Reg #: 3023102955 · FEI: 3023102955 · Expires 2026
    View on FDA
    Products
    10
    Proprietary Names
    5
    Establishment Types
    1
    Classifications
    10

    Registration Details

    Registration Name
    CHG-MERIDIAN CANADA LTD
    Registration Number
    3023102955
    FEI Number
    3023102955
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    1 Robert Speck Parkway, Suite No. 960
    City
    Mississauga Ontario
    Country
    CA

    Regulatory Submissions

    510(k) Number
    K121959

    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
    Endoscope, Accessories, Narrow Band Spectrum NWB
    Bronchoscope (Flexible Or Rigid) EOQ
    Unit, Electrosurgical, Endoscopic (With Or Without Accessories) KNS
    Forceps, Biopsy, Electric KGE
    Kit, Nephroscope FGA
    Cystoscope And Accessories, Flexible/Rigid FAJ
    Snare, Flexible FDI
    Forceps, Biopsy, Non-Electric FCL
    Nasopharyngoscope (Flexible Or Rigid) EOB
    Colonoscope And Accessories, Flexible/Rigid FDF

    Proprietary Names

    Scope Broncho Video Scope Cysto Battery Fiberoptic Scope Cysto Videoscope Scope Rhino Fiberoptic Scope Colono Video Scope

    Establishment Types

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