Australia TGA ARTG record

Vibratory intravascular recanalization system catheter

Australia TGA ARTG Registered Device · Bard Australia Pty Ltd · Bard Peripheral Vascular Inc · Class IIb · Started November 18, 2022

Good Name: Bard Australia Pty Ltd - Vibratory intravascular recanalization system catheter

Device classification

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

Registration information

Start Date: November 18, 2022
Effective Date: November 18, 2022

Sponsor

Name: Bard Australia Pty Ltd

Manufacturer

Name: Bard Peripheral Vascular Inc
Country: United States of America
Address: 1625 West 3rd Street, Tempe, AZ, 85281

Intended purpose

Used in combination with the Recanalization System to facilitate the intra-luminal placement of conventional guidewires beyond peripheral artery chronic total occlusions via atherectomy

About this record

Access comprehensive regulatory information for Vibratory intravascular recanalization system catheter in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is sponsored by Bard Australia Pty Ltd, manufactured by Bard Peripheral Vascular Inc in United States of America. The device registration started on November 18, 2022.

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.