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Epic™ Over-the-wire Self-Expanding Nitinol Vascular Stent with Delivery System - Multiple peripheral arteries stent - ARTG 468825

Access comprehensive regulatory information for Epic™ Over-the-wire Self-Expanding Nitinol Vascular Stent with Delivery System - Multiple peripheral arteries stent in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is registered under ARTG number 468825 and sponsored by Boston Scientific Pty Ltd, manufactured by Boston Scientific Corporation in United States of America. The device registration started on November 15, 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.

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Class III
ARTG 468825
Class III
Epic™ Over-the-wire Self-Expanding Nitinol Vascular Stent with Delivery System - Multiple peripheral arteries stent
ARTG ID: 468825
Good Name: Boston Scientific Pty Ltd - Epic™ Over-the-wire Self-Expanding Nitinol Vascular Stent with Delivery System - Multiple peripheral arteries stent
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Intended Purpose

The Epic™ Over-the-wire Self-Expanding Nitinol Vascular Stent with Delivery System is indicated to improve luminal diameter in the treatment of adults with de-novo or restenotic lesions in the iliac arteries, superficial femoral artery (SFA), and/or proximal popliteal artery (PPA).

Device Classification
Risk Class
Class III
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
468825
Start Date
November 15, 2024
Effective Date
November 15, 2024
Manufacturer
Country
United States of America
Address
300 Boston Scientific Way, Marlborough, MA, 01752