BEUDAMED
    FDA Registration Active 🇺🇸 United States

    ADVIA Centaur Creatine Kinase MB (CKMB)

    Reg #: 1219913 · FEI: 1219913 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    8
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    Siemens Healthcare Diagnostics Inc.
    Registration Number
    1219913
    FEI Number
    1219913
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    333 Coney Street
    City
    E Walpole
    State
    MA
    ZIP
    02032
    Country
    US

    Regulatory Submissions

    510(k) Number
    K962126

    Owner / Operator

    Firm Name
    SIEMENS HEALTHCARE DIAGNOSTICS INC.
    Operator Number
    9096044
    Address
    Siemens Healthcare Diagnostics Inc., 511 Benedict Avenue
    City
    Tarrytown
    State
    NY
    Postal Code
    10591
    Country
    US
    Correspondent
    Mary Seeger

    Products

    Device Name Product Code
    Differential Rate Kinetic Method, Cpk Or Isoenzymes JHS
    Fluorometric Method, Cpk Or Isoenzymes JHX

    Proprietary Names

    ADVIA Centaur Creatine Kinase MB (CKMB) Atellica IM Creatine Kinase MB (CKMB) Atellica IM Creatine Kinase MB Diluent (CKMB Dil) ADVIA Centaur Creatine Kinase MB Diluent (CKMB Dil) ADVIA Centaur Creatine Kinase MB Calibrator (CKMB CAL) Atellica IM Creatine Kinase MB Calibrator (CKMB CAL) ADVIA Centaur Creatine Kinase MB Master Curve Material (CKMB MCM) Atellica IM Creatine Kinase MB Master Curve Material (CKMB MCM)

    Establishment Types

    Manufacture Medical Device