BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Leishmania Serum ELISA Test Kit

    Reg #: 3011527950 · FEI: 3011527950 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    NEW LIFE DIAGNOSTICS INC.
    Registration Number
    3011527950
    FEI Number
    3011527950
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    5909 Sea Lion Pl, Suite A
    City
    Carlsbad
    State
    CA
    ZIP
    92010
    Country
    US

    Owner / Operator

    Firm Name
    New Life Diagnostics. Inc.
    Operator Number
    10048943
    Address
    5909 Sea Lion Place, Suite A
    City
    Carlsbad
    State
    CA
    Postal Code
    92010
    Country
    US
    Correspondent
    Michelle Y Larmour

    Products

    Device Name Product Code
    Reagent, Leishmanii Serological LOO

    Proprietary Names

    Leishmania Serum ELISA Test Kit

    Establishment Types

    Manufacture Device in the United States for Export Only