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Transducer assembly, ultrasound, diagnostic, intracorporeal, surgical - ARTG 461916

Access comprehensive regulatory information for Transducer assembly, ultrasound, diagnostic, intracorporeal, surgical in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 461916 and sponsored by Fujifilm Australia Pty Ltd, manufactured by Fujifilm Corporation in Japan. The device registration started on September 03, 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 IIa
ARTG 461916
Class IIa
Transducer assembly, ultrasound, diagnostic, intracorporeal, surgical
ARTG ID: 461916
Good Name: Fujifilm Australia Pty Ltd - Transducer assembly, ultrasound, diagnostic, intracorporeal, surgical
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Intended Purpose

The subject surgical ultrasound imaging probes are intended to be placed within a patient's surgical site for localised intra-operative imaging applications.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
461916
Start Date
September 03, 2024
Effective Date
September 03, 2024
Manufacturer
Country
Japan
Address
26-30 Nishiazabu 2 Chome, MINATO KU TOKYO, 106 8620