ARTG 436530Bone grafting cannula
ARTG ID: 436530 · Actis Medical Pty Ltd · Silony Medical GmbH · Class IIa · Started January 22, 2024
Good Name: Actis Medical Pty Ltd - Bone grafting cannula
- Risk Class
- Class IIa
- Product Type
- Single Device Product
- ARTG Category
- General
- ARTG ID
- 436530
- Start Date
- January 22, 2024
- Effective Date
- January 22, 2024
- Country
- Germany
- Address
- Leinfelder Strasse 60, Leinfelden-Echterdingen, 70771
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.
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 registered under ARTG number 436530 and 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.