BEUDAMED
    FDA Registration Active 🇨🇦 Canada

    Scope Cysto Battery Fiberoptic

    Reg #: 3023102955 · FEI: 3023102955 · Expires 2025
    View on FDA
    Products
    6
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    6

    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
    K032092

    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
    Forceps, Biopsy, Electric KGE
    Unit, Electrosurgical, Endoscopic (With Or Without Accessories) KNS
    Cystoscope And Accessories, Flexible/Rigid FAJ
    Kit, Nephroscope FGA
    Forceps, Biopsy, Non-Electric FCL
    Snare, Flexible FDI

    Proprietary Names

    Scope Cysto Battery Fiberoptic

    Establishment Types

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