BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Arrow Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) ARROWg+ard Blue Plus(R) Catheter

    Reg #: 3010425778 · FEI: 3010425778 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    16
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Teleflex LLC (NADC 2)
    Registration Number
    3010425778
    FEI Number
    3010425778
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    11245 N. Distribution Cove
    City
    Olive Branch
    State
    MS
    ZIP
    38654
    Country
    US

    Regulatory Submissions

    510(k) Number
    K993691

    Owner / Operator

    Firm Name
    Arrow International LLC (subsidiary of Teleflex Incorporated
    Operator Number
    2518433
    Address
    3015 Carrington Mill Blvd.
    City
    Morrisville
    State
    NC
    Postal Code
    27560
    Country
    US
    Correspondent
    Divya Raman

    Products

    Device Name Product Code
    Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days FOZ

    Proprietary Names

    Arrow Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) ARROWg+ard Blue Plus(R) Catheter ARROWg+ard Blue Plus Multi-Lumen CVC Super Kit ARROWg+ard Blue Plus Quad-Lumen CVC Set ARROWg+ard Blue Plus Multi-Lumen CVC Set ARROWg+ard Blue Plus Two-Lumen CVC ARROWg+ard Blue Plus Multi-Lumen CVC Extreme Kit ARROWg+ard Blue Plus Quad-Lumen CVC AGB+ Two-Lumen CVC Kit Ag+ Blue Plus ML CVCs ARROWg+ard Blue Plus Two-Lumen CVC Super Kit ARROWg+ard Blue Plus Two-Lumen CVC Kit ARROWg+ard Blue Plus Quad-Lumen CVC Super Kit ARROWg+ard Blue Plus Multi-Lumen CVC Kit ARROWg+ard Blue Plus Two-Lumen CVC Set AGB+ Quad Lumen CVC Kit AGB+ Multi-Lumen CVC Kit

    Establishment Types

    Repack or Relabel Medical Device