BEUDAMED
    FDA Registration Active 🇲🇺 Mauritius

    STOPLOSS, 3.5MM 10MM

    Reg #: 3004467263 · FEI: 3004467263 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    30
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    FCI SUD
    Registration Number
    3004467263
    FEI Number
    3004467263
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    VEL INDUSTRIAL COMPLEX, ROYAL ROAD
    City
    MAPOU LECLEZIO GOODLANDS Riviere du Rempart
    Country
    MU

    Regulatory Submissions

    510(k) Number
    K140290

    Owner / Operator

    Firm Name
    Carl Zeiss Meditec, Inc.
    Operator Number
    9053564
    Address
    5300 Central Parkway
    City
    Dublin
    State
    CA
    Postal Code
    94568
    Country
    US

    US Agent

    Business Name
    CARL ZEISS MEDITEC USA, INC.
    Contact Name
    Paul Swift
    Address
    5300 Central Parkway
    City
    Dublin
    State
    CA
    ZIP
    94568
    Country
    US
    Email
    [email protected]
    Phone
    817 9258507

    Products

    Device Name Product Code
    Lacrimal Stents And Intubation Sets OKS

    Proprietary Names

    STOPLOSS, 3.5MM 10MM STOPLOSS, 3.5MM 9MM STOPLOSS, 3.5MM 22MM STOPLOSS, 3.5MM 21MM STOPLOSS, 4MM 13MM STOPLOSS, 4MM 9MM STOPLOSS, 4MM 20MM STOPLOSS, 3.5MM 15MM STOPLOSS, 4MM 15MM STOPLOSS, 3.5MM 14MM STOPLOSS, 3.5MM 20MM STOPLOSS, 4MM 17MM STOPLOSS, 4MM 11MM STOPLOSS, 3.5MM 18MM STOPLOSS, 4MM 14MM STOPLOSS JONES TUBE INTRODUCER SET STOPLOSS, 3.5MM 17MM STOPLOSS, 3.5MM 12MM STOPLOSS, 3.5MM 19MM STOPLOSS, 4MM 21MM STOPLOSS, 4MM 12MM STOPLOSS, 3.5MM 11MM STOPLOSS, 4MM 16MM STOPLOSS, 4MM 18MM STOPLOSS, 4MM 10MM STOPLOSS JONES TUBE REMOVAL TOOL STOPLOSS, 3.5MM 16MM STOPLOSS, 4MM 19MM STOPLOSS, 3.5MM 13MM STOPLOSS, 4MM 22MM

    Establishment Types

    Manufacture Medical Device