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Verticale Reusable Instruments - Fixation system implantation kit, internal

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.

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TGA ARTG Official Data
Class I
Class I
Verticale Reusable Instruments - Fixation system implantation kit, internal
Australia TGA ARTG Registered Device
Good Name: Actis Medical Pty Ltd - Verticale Reusable Instruments - Fixation system implantation kit, internal
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Intended Purpose

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

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
Manufacturer
Country
Germany
Address
Leinfelder Strasse 60, Leinfelden-Echterdingen, 70771