BEUDAMED
    FDA Registration Active 🇩🇪 Germany

    FRESENIUS KABI DEUTSCHLAND GMBH

    Reg #: 9681819 · FEI: 3000147578 · Expires 2026
    View on FDA
    Products
    4
    Proprietary Names
    6
    Establishment Types
    1
    Classifications
    4

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    Registration Details

    Registration Name
    FRESENIUS KABI DEUTSCHLAND GMBH
    Registration Number
    9681819
    FEI Number
    3000147578
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    5 ROBERT-KOCH-STRASSE
    City
    BAD HERSFELD Hesse
    Country
    DE

    Regulatory Submissions

    510(k) Number
    K221121

    Owner / Operator

    Firm Name
    Fresenius Kabi AG
    Operator Number
    9027285
    Address
    Else-Kroner-Str. 1
    City
    61352 Bad Homburg
    State
    DE-NOTA
    Postal Code
    NONE
    Country
    DE

    Products

    Device Name Product Code
    Set, Administration, Intravascular FPA
    Set, I.V. Fluid Transfer LHI
    Catheter, Irrigation GBX
    Pump, Infusion FRN

    Proprietary Names

    Volumat Line freeflex+ Transfer Adapter Transfer Set VOLUMAT MC AGILIA VOLUMAT LINES K-Zero Needleless Connector

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility