BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Selectra Guiding Catheters

    Reg #: 1028232 · FEI: 1028232 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    3
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    BIOTRONIK, INC.
    Registration Number
    1028232
    FEI Number
    1028232
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    6024 JEAN RD.
    City
    LAKE OSWEGO
    State
    OR
    ZIP
    97035
    Country
    US

    Regulatory Submissions

    510(k) Number
    K183265

    Owner / Operator

    Firm Name
    BIOTRONIK, INC.
    Operator Number
    1028232
    Address
    6024 JEAN RD., --
    City
    Lake Oswego
    State
    OR
    Postal Code
    97035
    Country
    US
    Correspondent
    JON - BRUMBAUGH

    Products

    Device Name Product Code
    Catheter, Percutaneous DQY

    Proprietary Names

    Selectra Guiding Catheters Selectra Slitter Tool Selectra Accessory Kit

    Establishment Types

    Repack or Relabel Medical Device