BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Duo Venous Stent System

    Reg #: 3017390540 · FEI: 3017390540 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    VESPER MEDICAL, INC.
    Registration Number
    3017390540
    FEI Number
    3017390540
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    5905 Nathan Ln N
    City
    Plymouth
    State
    MN
    ZIP
    55442
    Country
    US

    Regulatory Submissions

    PMA Number
    P230021

    Owner / Operator

    Firm Name
    Vesper Medical, Inc.
    Operator Number
    10077776
    Address
    222 Jacobs St
    City
    Cambridge
    State
    MA
    Postal Code
    02141
    Country
    US
    Correspondent
    Jayshree Patel

    Products

    Device Name Product Code
    Stent, Iliac Vein QAN

    Proprietary Names

    Duo Venous Stent System

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility