BEUDAMED
    FDA Registration Active 🇺🇸 United States

    MINNESOTA MEDTEC, INC.

    Reg #: 2134626 · FEI: 3003007911 · Expires 2026
    View on FDA
    Products
    4
    Proprietary Names
    1
    Establishment Types
    2
    Classifications
    4

    Registration Details

    Registration Name
    MINNESOTA MEDTEC, INC.
    Registration Number
    2134626
    FEI Number
    3003007911
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    11760 Justen Circle, Mail drop Unit B
    City
    MAPLE GROVE
    State
    MN
    ZIP
    55369
    Country
    US

    Owner / Operator

    Firm Name
    MINNESOTA MEDTEC, INC.
    Operator Number
    9036710
    Address
    11760 JUSTEN CIRCLE UNIT B, --
    City
    Osseo
    State
    MN
    Postal Code
    55369
    Country
    US
    Correspondent
    BRIAN - PACKARD

    Products

    Device Name Product Code
    Percutaneous Sheath Introducer Kit OFL
    Occluder, Balloon, Vena-Cava LWT
    Monitor, Esophageal Motility, Anorectal Motility, And Tube KLA
    Catheter, Angioplasty, Peripheral, Transluminal LIT

    Proprietary Names

    MCOMPASS

    Establishment Types

    Manufacture Device in the United States for Export Only Manufacture Medical Device for Another Party (Contract Manufacturer)