Australia TGA ARTG record

Peripheral intravenous cannula

Australia TGA ARTG Registered Device · Smiths Medical Australasia Pty Ltd · Smiths Medical ASD Inc · Class IIb · Started May 31, 2024

Good Name: Smiths Medical Australasia Pty Ltd - Peripheral intravenous cannula

Device classification

Risk Class: Class IIb
Product Type: Single Device Product
ARTG Category: General

Registration information

Start Date: May 31, 2024
Effective Date: May 31, 2024

Sponsor

Name: Smiths Medical Australasia Pty Ltd

Manufacturer

Name: Smiths Medical ASD Inc
Country: United States of America
Address: 6000 Nathan Lane North , Minneapolis, MN, 55442

Intended purpose

The POWERWAND™ XL Introducer with Extended Dwell Catheter made of ChronoFlex C® with BioGUARD™ Technology is used to gain access to the vascular system to sample blood and administer fluids intravenously. It may also be used for power injection of contrast media up to a rate of 8 ml/sec, at a maximum of 325 psi fluid pressure.

About this record

Access comprehensive regulatory information for Peripheral intravenous cannula in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is sponsored by Smiths Medical Australasia Pty Ltd, manufactured by Smiths Medical ASD Inc in United States of America. The device registration started on May 31, 2024.

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.