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Orthopaedic cement injection cannula

Access comprehensive regulatory information for Orthopaedic cement injection 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.

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Class IIa
Class IIa
Orthopaedic cement injection cannula
Australia TGA ARTG Registered Device
Good Name: Actis Medical Pty Ltd - Orthopaedic cement injection cannula
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Intended Purpose

A sterile tube that is attached to the distal end of an orthopaedic cement dispenser and through which the bone cement is dispensed to the target site. This is intended to be used during spine surgery. This is a single-use device.

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