BEUDAMED
    FDA Registration Active 🇩🇪 Germany

    KBL 8000 alpha hybridSun

    Reg #: 3006116732 · FEI: 3006116732 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    9
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    KBL GmbH
    Registration Number
    3006116732
    FEI Number
    3006116732
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Ringstrasse 24-26
    City
    Dernbach Rhineland-Palatinate
    Country
    DE

    Regulatory Submissions

    510(k) Number
    K191881

    Owner / Operator

    Firm Name
    KBL GmbH
    Operator Number
    10030591
    Address
    Ringstrasse 24-26
    City
    Dernbach
    State
    Rhineland-Palatinate
    Postal Code
    56307
    Country
    DE
    Correspondent
    Ralf de Andreis

    US Agent

    Business Name
    Bentley Biomedical Consulting LLC
    Contact Name
    Shepard Bentley
    Address
    28241 Crown Valley Parkway, Suite 510(k)
    City
    Laguna Niguel
    State
    CA
    ZIP
    92677
    Country
    US
    Email
    [email protected]
    Phone
    949 3749187

    Products

    Device Name Product Code
    Booth, Sun Tan LEJ

    Proprietary Names

    KBL 8000 alpha hybridSun KBL 7900 alpha hybridSun KBL 7000 alpha hybridSun KBL P9 hybridSun KBL P9S hybridSun KBL K5 hybridSun KBL K7S hybridSun KBL K7 hybridSun KBL K9S hybridSun

    Establishment Types

    Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device