Australia TGA ARTG record

Bone grafting cannula

Australia TGA ARTG Registered Device · Actis Medical Pty Ltd · Silony Medical GmbH · Class IIa · Started January 22, 2024

Good Name: Actis Medical Pty Ltd - Bone grafting cannula

Device classification

Risk Class: Class IIa
Product Type: Single Device Product
ARTG Category: General

Registration information

Start Date: January 22, 2024
Effective Date: January 22, 2024

Sponsor

Name: Actis Medical Pty Ltd

Manufacturer

Name: Silony Medical GmbH
Country: Germany
Address: Leinfelder Strasse 60, Leinfelden-Echterdingen, 70771

Intended purpose

A rigid, single use metal tube intended to be used surgically to introduce bone substitute to fill gaps in the bone structure created during orthopaedic surgical procedures, particularly of the spine.

About this record

Access comprehensive regulatory information for Bone grafting cannula in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Actis Medical Pty Ltd, manufactured by Silony Medical GmbH in Germany. The device registration started on January 22, 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.