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Option Elite 100cm Retievable Vena Cava Filter System - Vena cava filter, optional - ARTG 284696

Access comprehensive regulatory information for Option Elite 100cm Retievable Vena Cava Filter System - Vena cava filter, optional in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is registered under ARTG number 284696 and sponsored by Life Healthcare Pty Ltd, manufactured by Argon Medical Devices Inc in United States of America. The device registration started on January 17, 2017.

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 284696
Class III
Option Elite 100cm Retievable Vena Cava Filter System - Vena cava filter, optional
ARTG ID: 284696
Good Name: Life Healthcare Pty Ltd - Option Elite 100cm Retievable Vena Cava Filter System - Vena cava filter, optional
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Intended Purpose

The Optionโ„ข ELITE Vena Cava Filter 100cm System is intended for the prevention of recurrent pulmonary embolism (PE) via placement in the vena cava in the following conditions: - Pulmonary thromboembolism when anticoagulant therapy is contraindicated, - Failure of anticoagulant therapy in thromboembolic diseases, - Emergency treatment following massive pulmonary embolism where anticipated benefits of conventional therapy are reduced, - Chronic, recurrent pulmonary embolism when anticoagulant therapy has failed or is contraindicated. The Filter may be removed according to supplied instructions in patients who no longer require a filter. Retrieval of the filter can only be performed by the jugular approach. The Angiographic Vessel Dilator is designed to provide angiographic visualization and linear measurement of the vasculature when used in conjunction with the delivery of radiopaque contrast media to the vena cava.

Device Classification
Risk Class
Class III
Product Type
Medical device system
ARTG Category
General
Registration Information
ARTG ID
284696
Start Date
January 17, 2017
Effective Date
January 17, 2017
Manufacturer
Country
United States of America
Address
1445 Flat Creek Road, Athens, Texas, 75751