BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Site-Rite Needle Guide Kits and Pro

    Reg #: 3013041594 · FEI: 3013041594 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Dymax, Corp.
    Registration Number
    3013041594
    FEI Number
    3013041594
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    141 Zehner School Rd
    City
    Zelienople
    State
    PA
    ZIP
    16063
    Country
    US

    Regulatory Submissions

    510(k) Number
    K042445

    Owner / Operator

    Firm Name
    C. R. Bard, Inc.
    Operator Number
    2212754
    Address
    1 Becton Drive
    City
    Franklin Lakes
    State
    NJ
    Postal Code
    07417
    Country
    US

    Products

    Device Name Product Code
    Transducer, Ultrasonic, Diagnostic ITX

    Proprietary Names

    Site-Rite Needle Guide Kits and Pro

    Establishment Types

    Repack or Relabel Medical Device