BEUDAMED
    FDA Registration Active 🇺🇸 United States

    nGen Pump

    Reg #: 3010653929 · FEI: 3010653929 · Expires 2025
    View on FDA
    Products
    3
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    3

    Registration Details

    Registration Name
    Stellartech Research Corp.
    Registration Number
    3010653929
    FEI Number
    3010653929
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    560 Cottonwood Dr
    City
    Milpitas
    State
    CA
    ZIP
    95035
    Country
    US

    Regulatory Submissions

    PMA Number
    P990071

    Owner / Operator

    Firm Name
    STELLARTECH RESEARCH CORP.
    Operator Number
    9022137
    Address
    560 Cottonwood Drive, --
    City
    Milpitas
    State
    CA
    Postal Code
    95035
    Country
    US
    Correspondent
    Derek Purdy

    Products

    Device Name Product Code
    Cardiac Ablation Percutaneous Catheter LPB
    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter OAD
    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation OAE

    Proprietary Names

    nGen Pump

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)