BEUDAMED
    FDA Registration Active 🇺🇸 United States

    NOVO VIVO SUCTON CATHETER

    Reg #: 2183741 · FEI: 2183741 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    GENESIS INDUSTRIES, INC.
    Registration Number
    2183741
    FEI Number
    2183741
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    601 PRO-JECT DR.
    City
    ELMWOOD
    State
    WI
    ZIP
    54740
    Country
    US

    Owner / Operator

    Firm Name
    GENESIS INDUSTRIES, INC.
    Operator Number
    2183741
    Address
    303 SOUTH MCKAY AVE.,, P.O. BOX 39
    City
    SPRING VALLEY
    State
    WI
    Postal Code
    54767
    Country
    US

    Products

    Device Name Product Code
    Catheter, Ventricular, General & Plastic Surgery GBS

    Proprietary Names

    NOVO VIVO SUCTON CATHETER

    Establishment Types

    Manufacture Medical Device