BEUDAMED
    FDA Registration Active 🇯🇵 Japan

    Lumipulse G ?-Amyloid Ratio (1-42/1-40)

    Reg #: 3002895169 · FEI: 3002895169 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    4
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Fujirebio Inc.
    Registration Number
    3002895169
    FEI Number
    3002895169
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1-3-14 Tanashioda, Chuo-ku
    City
    Sagamihara Kanagawa
    Country
    JP

    Regulatory Submissions

    510(k) Number
    DEN200072

    Owner / Operator

    Firm Name
    Fujirebio Diagnostics, Inc.
    Operator Number
    10022860
    Address
    201 Great Valley Parkway
    City
    Malvern
    State
    PA
    Postal Code
    19355
    Country
    US

    US Agent

    Business Name
    Fujirebio Diagnostics, Inc.
    Contact Name
    Greg Dickson
    Address
    201 Great Valley Parkway
    City
    Malvern
    State
    PA
    ZIP
    19355
    Country
    US
    Email
    [email protected]
    Phone
    610 2403888

    Products

    Device Name Product Code
    Alzheimer’S Disease Pathology Assessment Test QSE

    Proprietary Names

    Lumipulse G ?-Amyloid Ratio (1-42/1-40) Lumipulse G ?-Amyloid Immunoreaction Cartridges 1-42 Lumipulse G ?-Amyloid Immunoreaction Cartridges 1-40 Lumipulse G ?-Amyloid Calibrators

    Establishment Types

    Manufacture Medical Device