BEUDAMED
    FDA Registration Active 🇩🇪 Germany

    EUROIMMUN Analyzer I-2P

    Reg #: 3007361513 · FEI: 3007361513 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    11
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    EUROIMMUN Medizinische Labordiagnostika AG
    Registration Number
    3007361513
    FEI Number
    3007361513
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    EUROIMMUN AG, Werkstrasse 1
    City
    Dassow Mecklenburg-Western Pomerania
    Country
    DE

    Owner / Operator

    Firm Name
    EUROIMMUN Medizinische Labordiagnostika AG
    Operator Number
    10025212
    Address
    EUROIMMUN AG, Seekamp 31
    City
    Luebeck
    State
    Schleswig-Holstein
    Postal Code
    D-23560
    Country
    DE
    Correspondent
    Stephan Maihold

    Products

    Device Name Product Code
    Analyzer, Chemistry (Photometric, Discrete), For Clinical Use JJE

    Proprietary Names

    EUROIMMUN Analyzer I-2P EUROIMMUN Analyzer I EUROBlotOne EUROLabWorkstation ELISA Device Qualification Test Kit EUROLabLiquidHandler IF Sprinter Device Qualification Test Kit EUROLabWorkstation IFA Device Qualification Test Kit EUROLabWorkstation ELISA Device Qualification Test Kit EUROIMMUN Analyzer I / I-2P System liquid concentrate Sprinter XL

    Establishment Types

    Manufacture Medical Device