E-tegra Stent Graft System – Aortic Extension - Abdominal aortic aneurysm stent - ARTG 388372
Access comprehensive regulatory information for E-tegra Stent Graft System – Aortic Extension - Abdominal aortic aneurysm stent in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is registered under ARTG number 388372 and sponsored by Cryolife Medical (Australia) Company Pty Ltd, manufactured by Jotec GmbH in Germany. The device registration started on May 12, 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.
The E-tegra Stent Graft System is indicated for the endovasculartreatment of infrarenal aortic aneurysms. These aneurysms can alsoaffect the common iliac artery.