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Arthrex® Univers Revers™ Modular Glenoid System Monoblock Post Baseplate - Reverse shoulder prosthesis base plate - ARTG 481525

Access comprehensive regulatory information for Arthrex® Univers Revers™ Modular Glenoid System Monoblock Post Baseplate - Reverse shoulder prosthesis base plate in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is registered under ARTG number 481525 and sponsored by Arthrex Australia Pty Ltd, manufactured by Arthrex Inc in United States of America. The device registration started on March 03, 2025.

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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TGA ARTG Official Data
Class III
ARTG 481525
Class III
Arthrex® Univers Revers™ Modular Glenoid System Monoblock Post Baseplate - Reverse shoulder prosthesis base plate
ARTG ID: 481525
Good Name: Arthrex Australia Pty Ltd - Arthrex® Univers Revers™ Modular Glenoid System Monoblock Post Baseplate - Reverse shoulder prosthesis base plate
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Intended Purpose

The Arthrex® Univers Revers™ Modular Glenoid System Monoblock Post Baseplate is indicated for use in a grossly rotator cuff deficient glenohumeral joint with severe arthropathy or a previously failed joint replacement with a gross rotator cuff deficiency.The patient’s joint must be anatomically and structurally suited to receive the selected implant(s), and a functional deltoid muscle is necessary to use the device. The Univers Revers Modular Glenoid System is indicated for primary or revision total shoulder replacement for the relief of pain and significant disability due to gross rotator cuff deficiency. The Univers Revers Modular Glenoid System is porous coated and is intended for cementless use with the addition of screws for fixation.

Device Classification
Risk Class
Class III
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
481525
Start Date
March 03, 2025
Effective Date
March 03, 2025
Manufacturer
Country
United States of America
Address
1370 Creekside Boulevard, Naples, Florida, 34108-1945