BEUDAMED
    FDA Registration Active 🇨🇦 Canada

    EpiZact

    Reg #: 3029960285 · FEI: 3029960285 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    GUIDESTAR MEDICAL DEVICES INC.
    Registration Number
    3029960285
    FEI Number
    3029960285
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    201-2067 Cadboro Bay Rd
    City
    Victoria British Columbia
    Country
    CA

    Regulatory Submissions

    510(k) Number
    K233056

    Owner / Operator

    Firm Name
    GuideStar Medical Devices Inc.
    Operator Number
    10089132
    Address
    201-2067 Cadboro Bay Rd
    City
    Victoria
    State
    British Columbia
    Postal Code
    V8R5G4
    Country
    CA
    Correspondent
    Michael Dolphin

    US Agent

    Business Name
    Lean RAQA, LLC
    Contact Name
    Michelle Lott
    Address
    131 E Loch Lomond Pl
    City
    Tucson
    State
    AZ
    ZIP
    85737
    Country
    US
    Email
    [email protected]
    Phone
    520 2759838

    Products

    Device Name Product Code
    Syringe, Piston FMF

    Proprietary Names

    EpiZact

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility