BEUDAMED
    FDA Registration Active 🇩🇪 Germany

    MeKo Manufacturing e.K.

    Reg #: 3009937642 · FEI: 3009937642 · Expires 2026
    View on FDA
    Products
    1
    Proprietary Names
    0
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    MeKo Manufacturing e.K.
    Registration Number
    3009937642
    FEI Number
    3009937642
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    Im Kirchenfelde 12-14
    City
    Sarstedt Lower Saxony
    Country
    DE

    Owner / Operator

    Firm Name
    MeKo Manufacturing e.K.
    Operator Number
    10044323
    Address
    Im Kirchenfelde 12-14
    City
    Sarstedt
    State
    Lower Saxony
    Postal Code
    31157
    Country
    DE

    US Agent

    Business Name
    MeKo MedTech Inc
    Contact Name
    Tim Fries
    Address
    8500 Normandale Lake Blvd Ste 350
    City
    Bloomington
    State
    MN
    ZIP
    55437
    Country
    US
    Email
    [email protected]
    Phone
    612 2409392

    Products

    Device Name Product Code
    Iliac Covered Stent, Arterial PRL

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)