Australia TGA ARTG record

Verticale Reusable Instruments - Fixation system implantation kit, internal

Australia TGA ARTG Registered Device · 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

Device classification

Risk Class: Class I
Product Type: Medical device system
ARTG Category: General

Registration information

Start Date: January 31, 2024
Effective Date: January 31, 2024

Sponsor

Name: Actis Medical Pty Ltd

Manufacturer

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

Intended purpose

A system of various surgical instruments intended to be used to perform orthopaedic surgical procedures. Devices are reusable.

About this record

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 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.