BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Lumipulse G Wash Solution 4008248

    Reg #: 1643621 · FEI: 1643621 · Expires 2025
    View on FDA
    Products
    3
    Proprietary Names
    7
    Establishment Types
    1
    Classifications
    3

    Registration Details

    Registration Name
    Fujirebio Diagnostics, Inc.
    Registration Number
    1643621
    FEI Number
    1643621
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    940 Crossroads Blvd
    City
    Seguin
    State
    TX
    ZIP
    78155
    Country
    US

    Regulatory Submissions

    510(k) Number
    K142895

    Owner / Operator

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

    Products

    Device Name Product Code
    Calibrator, Secondary JIT
    Analyzer, Chemistry (Photometric, Discrete), For Clinical Use JJE
    Test, Epithelial Ovarian Tumor-Associated Antigen (Ca125) LTK

    Proprietary Names

    Lumipulse G Wash Solution 4008248 Lumipulse G CA125II Calibrators Lumipulse G1200 Instrument Lumipulse G CA125II IC Specimen Diluent 1 Substrate Solutions Lumipulse G Wash Solution 231173

    Establishment Types

    Manufacture Medical Device