BEUDAMED
    FDA Registration Active 🇮🇹 Italy

    ADRIA SRL.

    Reg #: 3014200871 · FEI: 3014200871 · Expires 2026
    View on FDA
    Products
    6
    Proprietary Names
    9
    Establishment Types
    1
    Classifications
    6

    Registration Details

    Registration Name
    ADRIA SRL.
    Registration Number
    3014200871
    FEI Number
    3014200871
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    Via Modena n. 46
    City
    San Giovanni in Persiceto Bologna
    Country
    IT

    Regulatory Submissions

    510(k) Number
    K141557

    Owner / Operator

    Firm Name
    Adria Srl.
    Operator Number
    10062522
    Address
    Via Modena n. 46
    City
    San Giovanni in Persiceto (BO)
    State
    IT-NOTA
    Postal Code
    40017
    Country
    IT

    US Agent

    Business Name
    Dumotech, LLC.
    Contact Name
    Duc Duong
    Address
    6758 East Pris Ave. SE
    City
    Caledonia
    State
    MI
    ZIP
    49316
    Country
    US
    Email
    [email protected]
    Phone
    800 9196101 ext. 122

    Products

    Device Name Product Code
    Arthroscope HRX
    Injector, Vertebroplasty (Does Not Contain Cement) OAR
    Bit, Drill HTW
    Collector, Urine, (And Accessories) For Indwelling Catheter KNX
    Spinal Channeling Instrument, Vertebroplasty OCJ
    Needle, Aspiration And Injection, Disposable GAA

    Proprietary Names

    Herniatome 5091715, 5091749, 5091745 Cement Injection Cannula - 495041420 Kit of 2 Cement delivery instruments - 495041123 Vertebroplasty Injector Kit - 49000001 Hollow Drill - 495930810 Litebag 500/0600 Vertebroplasty Needle Kit - 49225 Vertebroplasty Needle - 496xx, 498xx, 491xx, 490xx, 492xx, T0604xx Vertebroplasty Canulated Needle - 493xx, T0604xx

    Establishment Types

    Manufacture Medical Device