BEUDAMED
    FDA Registration Active 🇺🇸 United States

    PRO-TECH Design & Mfg, Inc.

    Reg #: 3010531069 · FEI: 3010531069 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    0
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    PRO-TECH Design & Mfg, Inc.
    Registration Number
    3010531069
    FEI Number
    3010531069
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    4041 Express Street
    City
    Arlington
    State
    TX
    ZIP
    76001
    Country
    US

    Regulatory Submissions

    510(k) Number
    K972665

    Owner / Operator

    Firm Name
    PRO-TECH Design & Mfg, Inc.
    Operator Number
    9048910
    Address
    14561 MARQUARDT AVE., --
    City
    Santa Fe Springs
    State
    CA
    Postal Code
    90670
    Country
    US

    Products

    Device Name Product Code
    Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass DWF

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)