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Vibratory intravascular recanalization system catheter

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.

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Class IIb
Class IIb
Vibratory intravascular recanalization system catheter
Australia TGA ARTG Registered Device
Good Name: Bard Australia Pty Ltd - Vibratory intravascular recanalization system catheter
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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

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
Manufacturer
Country
United States of America
Address
1625 West 3rd Street, Tempe, AZ, 85281