BEUDAMED
    FDA Registration Active 🇬🇧 United Kingdom

    Ortho Daily QC Simulated Whole Blood Quality Control Kit

    Reg #: 9610805 · FEI: 3002638287 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    MILLIPORE (UK) LTD
    Registration Number
    9610805
    FEI Number
    3002638287
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    FLEMING ROAD, KIRKTON CAMPUS
    City
    LIVINGSTON, W. LOTHIAN West Lothian
    Country
    GB

    Regulatory Submissions

    510(k) Number
    BK210653

    Owner / Operator

    Firm Name
    MilliporeSigma
    Operator Number
    1216103
    Address
    28820 Single Oak Drive
    City
    Temecula
    State
    CA
    Postal Code
    92590
    Country
    US
    Correspondent
    Catherine Karaman

    US Agent

    Business Name
    EMD MILLIPORE CORPORATION
    Contact Name
    Catherine Karaman
    Address
    28820 Single Oak Dr
    City
    Temecula
    State
    CA
    ZIP
    92590
    Country
    US
    Email
    [email protected]
    Phone
    951 2654660

    Products

    Device Name Product Code
    Kit, Quality Control For Blood Banking Reagents KSF

    Proprietary Names

    Ortho Daily QC Simulated Whole Blood Quality Control Kit

    Establishment Types

    Manufacture Medical Device