BEUDAMED
    FDA Registration Active 🇮🇳 India

    Model 5000/XX Series Multiplace Hyperbaric Chamber

    Reg #: 3013595329 · FEI: 3013595329 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    2
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Tekna Manufacturing Pvt. Ltd.
    Registration Number
    3013595329
    FEI Number
    3013595329
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    C19, Industrial Estate, Guindy
    City
    Chennai Tamil Nadu
    Country
    IN

    Regulatory Submissions

    510(k) Number
    K002794

    Owner / Operator

    Firm Name
    Tekna Manufacturing Pvt. Ltd
    Operator Number
    10045541
    Address
    C19, Industrial Estate, Guindy
    City
    Chennai
    State
    Tamil Nadu
    Postal Code
    600032
    Country
    IN
    Correspondent
    Sriram V Narasimhan

    US Agent

    Business Name
    Willow glen Consultancy llc
    Contact Name
    Willow Glen
    Address
    8880 Rio San Diego Dr Ste 800
    City
    San Diego
    State
    CA
    ZIP
    92108
    Country
    US
    Email
    [email protected]
    Phone
    619 8690249

    Products

    Device Name Product Code
    Chamber, Hyperbaric CBF

    Proprietary Names

    Model 5000/XX Series Multiplace Hyperbaric Chamber Modular Multiplace Hyperbaric Chamber

    Establishment Types

    Manufacture Medical Device