ARTG 439075Verticale Reusable Instruments - Fixation system implantation kit, internal
ARTG ID: 439075 · Actis Medical Pty Ltd · Silony Medical GmbH · Class I · Started January 31, 2024
Good Name: Actis Medical Pty Ltd - Verticale Reusable Instruments - Fixation system implantation kit, internal
- Risk Class
- Class I
- Product Type
- Medical device system
- ARTG Category
- General
- ARTG ID
- 439075
- Start Date
- January 31, 2024
- Effective Date
- January 31, 2024
- Country
- Germany
- Address
- Leinfelder Strasse 60, Leinfelden-Echterdingen, 70771
A system of various surgical instruments intended to be used to perform orthopaedic surgical procedures. Devices are reusable.
Access comprehensive regulatory information for Verticale Reusable Instruments - Fixation system implantation kit, internal in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 439075 and sponsored by Actis Medical Pty Ltd, manufactured by Silony Medical GmbH in Germany. The device registration started on January 31, 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.