BEUDAMED
    FDA Registration Active 🇩🇪 Germany

    STOCKERT GMBH

    Reg #: 3015537323 · FEI: 3015537323 · Expires 2025
    View on FDA
    Products
    4
    Proprietary Names
    0
    Establishment Types
    1
    Classifications
    4

    Registration Details

    Registration Name
    STOCKERT GMBH
    Registration Number
    3015537323
    FEI Number
    3015537323
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    BOETZINGER STRASSE 31
    City
    FREIBURG Baden-Wurttemberg
    Country
    DE

    Regulatory Submissions

    PMA Number
    P990071

    Owner / Operator

    Firm Name
    Stockert GmbH
    Operator Number
    9042012
    Address
    BOETZINGERSTR. 31, --
    City
    FREIBURG, B-W
    State
    DE-NOTA
    Postal Code
    D-79111
    Country
    DE
    Correspondent
    Christoph - Gerber

    US Agent

    Business Name
    MEDAGENT Inc.
    Contact Name
    Franz Menean
    Address
    264 Lafayette Rd Ste 7
    City
    Portsmouth
    State
    NH
    ZIP
    03801
    Country
    US
    Email
    [email protected]
    Phone
    603 5702039

    Products

    Device Name Product Code
    Cardiac Ablation Percutaneous Catheter LPB
    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter OAD
    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation OAE
    Catheter, Electrode Recording, Or Probe, Electrode Recording DRF

    Establishment Types

    Manufacture Medical Device