BEUDAMED
    FDA Registration Active 🇯🇵 Japan

    Perifix

    Reg #: 9680591 · FEI: 3005732259 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    8
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    B. BRAUN AESCULAP JAPAN CO., LTD.
    Registration Number
    9680591
    FEI Number
    3005732259
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    TOCHIGI FACTORY, 285 OGAKI,, TSUGA-MACHI, TOCHIGI-SHI
    City
    TOCHIGI
    Country
    JP

    Regulatory Submissions

    510(k) Number
    K813186

    Owner / Operator

    Firm Name
    B. BRAUN MELSUNGEN AG
    Operator Number
    8010484
    Address
    CARL-BRAUN-STR.1, --
    City
    MELSUNGEN
    State
    DE-NOTA
    Postal Code
    34212
    Country
    DE
    Correspondent
    Kamaal Anas

    US Agent

    Business Name
    B. BRAUN MEDICAL, INC.
    Contact Name
    Kamaal Anas
    Address
    824 Twelfth Avenue
    City
    Bethlehem
    State
    PA
    ZIP
    18018
    Country
    US
    Email
    [email protected]
    Phone
    484 5231349

    Products

    Device Name Product Code
    Anesthesia Conduction Kit CAZ

    Proprietary Names

    Perifix Perifix Catheter Perican Tuohy Needle Perifix Filter Sets Perifix Basic Single dose and continuous epidural tray Perifix mini sets Perifix continuous epidural tray Perifix Basic Intermediate dose and continuous epidural tray

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)