BEUDAMED
    FDA Registration Active 🇩🇪 Germany

    christoph miethke gmbh & co.kg

    Reg #: 3004721439 · FEI: 3004721439 · Expires 2026
    View on FDA
    Products
    3
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    3

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    Registration Details

    Registration Name
    christoph miethke gmbh & co.kg
    Registration Number
    3004721439
    FEI Number
    3004721439
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    ulanenweg 2, potsdam
    City
    potsdam Brandenburg
    Country
    DE

    Regulatory Submissions

    510(k) Number
    K120559

    Owner / Operator

    Firm Name
    christoph miethke gmbh & co.kg
    Operator Number
    10023285
    Address
    ulanenweg 2, potsdam
    City
    potsdam
    State
    Brandenburg
    Postal Code
    14469
    Country
    DE
    Correspondent
    joerg knebel

    US Agent

    Business Name
    Aesculap Inc.
    Contact Name
    Kamaal Anas
    Address
    3773 Corporate Parkway
    City
    Center Valley
    State
    PA
    ZIP
    18034
    Country
    US
    Email
    [email protected]
    Phone
    510 9849071 ext. 5071

    Products

    Device Name Product Code
    Shunt, Central Nervous System And Components JXG
    Instrument, Shunt System Implantation GYK
    Catheter, Ventricular HCA

    Proprietary Names

    Aesculap Miethke Ventricular Catheter

    Establishment Types

    Manufacture Medical Device