BEUDAMED
    FDA Registration Active 🇺🇸 United States

    K 600 LATEX TUBING

    Reg #: 3003502083 · FEI: 3003502083 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    5
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    KENT ELASTOMER PRODUCTS, INC.
    Registration Number
    3003502083
    FEI Number
    3003502083
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    7369 PEABODY-KENT RD.
    City
    WINESBURG
    State
    OH
    ZIP
    44690
    Country
    US

    Owner / Operator

    Firm Name
    KENT ELASTOMER PRODUCTS, INC.
    Operator Number
    9044738
    Address
    1500 ST. CLAIR AVE., --
    City
    Kent
    State
    OH
    Postal Code
    44240
    Country
    US
    Correspondent
    Brian Lipowski

    Products

    Device Name Product Code
    Catheter, Peritoneal GBW

    Proprietary Names

    K 600 LATEX TUBING KEP NON STERILE KEP NON-STERILE Penrose Drain Non-Sterile THERMOPLASTIC TUBING

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)