Australia TGA ARTG recordLarge-Bore CVC Set with Blue FlexTip ARROWg+ard Blue for High Volume Infusions - Central venous catheterization kit, short-term
Australia TGA ARTG Registered Device · Teleflex Medical Australia Pty Ltd · Arrow International LLC Subsidiary of Teleflex Incorporated · Class III · Started August 27, 2020
Good Name: Teleflex Medical Australia Pty Ltd - Large-Bore CVC Set with Blue FlexTip ARROWg+ard Blue for High Volume Infusions - Central venous catheterization kit, short-term
- Risk Class
- Class III
- Product Type
- Medical device system
- ARTG Category
- General
- Start Date
- August 27, 2020
- Effective Date
- August 27, 2020
- Country
- United States of America
- Address
- 3015 Carrington Mill Blvd, Morrisville, North Carolina, 27560
A collection of sterile devices and materials intended to provide short-term introduction of a central venous catheter for treatment of diseases or procedures requiring central venous access. The ARROWg+ard antimicrobial surface is intended to provide protection against catheter-related bloodstream infections. The large-bore multiple-lumen catheter permits venous access to the central circulation for rapid fluid administration. It may be inserted into the jugular, subclavian, or femoral veins.
Access comprehensive regulatory information for Large-Bore CVC Set with Blue FlexTip ARROWg+ard Blue for High Volume Infusions - Central venous catheterization kit, short-term in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is sponsored by Teleflex Medical Australia Pty Ltd, manufactured by Arrow International LLC Subsidiary of Teleflex Incorporated in United States of America. The device registration started on August 27, 2020.
This page provides complete registration details including sponsor information, manufacturer details, and regulatory compliance data from the official Australia TGA ARTG medical device database. Pure Global AI offers free access to Australia's complete medical device registry with 131,000+ devices, helping global MedTech companies navigate TGA regulations efficiently.