BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Scanlan Ligator

    Reg #: 2126670 · FEI: 2126670 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    2
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    SCANLAN INTERNATIONAL, INC.
    Registration Number
    2126670
    FEI Number
    2126670
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    1 SCANLAN PLZ
    City
    Saint Paul
    State
    MN
    ZIP
    55107
    Country
    US

    Owner / Operator

    Firm Name
    SCANLAN INTERNATIONAL, INC.
    Operator Number
    2126670
    Address
    ONE SCANLAN PLAZA, --
    City
    Saint Paul
    State
    MN
    Postal Code
    55107
    Country
    US

    Products

    Device Name Product Code
    Ligator, Hemorrhoidal FHN

    Proprietary Names

    Scanlan Ligator Scanturian™

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device