BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Stinger M

    Reg #: 1313046 · FEI: 1313046 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    9
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    C.R. BARD, INC.
    Registration Number
    1313046
    FEI Number
    1313046
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    289 Bay Rd
    City
    Queensbury
    State
    NY
    ZIP
    12804
    Country
    US

    Regulatory Submissions

    PMA Number
    P000020

    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
    Cardiac Ablation Percutaneous Catheter LPB

    Proprietary Names

    Stinger M Stinger SM Stinger Stinger S Scorpion TempLink M Extension Cables Scorpion 2 and Scorpion 2M Ablation distal tip electrodes & TempLink/ Catheters all with 4mm or 5mm

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)