BEUDAMED
    FDA Registration Active 🇬🇧 United Kingdom

    IMMULITE ACTH

    Reg #: 3002806944 · FEI: 3002806944 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    5
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED
    Registration Number
    3002806944
    FEI Number
    3002806944
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    GLYN RHONWY
    City
    LLANBERIS Wales
    Country
    GB

    Regulatory Submissions

    510(k) Number
    K960066

    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
    Radioimmunoassay, Acth CKG

    Proprietary Names

    IMMULITE ACTH IMMULITE 2000 ACTH IMMULITE IMMULITE/IMMULITE 1000 ACTH Sample Diluent ACTH Control

    Establishment Types

    Manufacture Medical Device