BEUDAMED
    FDA Registration Active 🇺🇸 United States

    ELIXIR MEDICAL CORPORATION

    Reg #: 3005092783 · FEI: 3005092783 · Expires 2026
    View on FDA
    Products
    3
    Proprietary Names
    0
    Establishment Types
    1
    Classifications
    3

    Registration Details

    Registration Name
    ELIXIR MEDICAL CORPORATION
    Registration Number
    3005092783
    FEI Number
    3005092783
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    920 N. McCarthy Blvd, Suite 100
    City
    Milpitas
    State
    CA
    ZIP
    95035
    Country
    US

    Owner / Operator

    Firm Name
    Elixir Medical Corporation
    Operator Number
    10027369
    Address
    920 N. McCarthy Blvd, Suite 100
    City
    Milpitas
    State
    CA
    Postal Code
    95035
    Country
    US

    Products

    Device Name Product Code
    Coronary Drug-Eluting Stent NIQ
    Shockwave Intravascular Lithotripsy System QMG
    Absorbable Coronary Drug-Eluting Stent PNY

    Establishment Types

    Manufacture Device in the United States for Export Only