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Internal spinal fixation procedure kit, reusable - ARTG 480505

Access comprehensive regulatory information for Internal spinal fixation procedure kit, reusable in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 480505 and sponsored by Evolution Surgical Pty Ltd, manufactured by SMAIO in France. The device registration started on February 24, 2025.

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 I
ARTG 480505
Class I
Internal spinal fixation procedure kit, reusable
ARTG ID: 480505
Good Name: Evolution Surgical Pty Ltd - Internal spinal fixation procedure kit, reusable
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Intended Purpose

A collection of various surgical instruments intended to be used to perform a bone-screw internal spinal fixation procedure. This is a reusable device.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
480505
Start Date
February 24, 2025
Effective Date
February 24, 2025
Manufacturer
Name
SMAIO
Country
France
Address
2 Place Berthe Morisot, Parc Technologique, SAINT PRIEST, 69800