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Diagnostic x-ray digital imaging conversion system - ARTG 308272

Access comprehensive regulatory information for Diagnostic x-ray digital imaging conversion system in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 308272 and sponsored by Shimadzu Medical Systems Oceania Pty Ltd, manufactured by Konica Minolta Inc in Japan. The device registration started on August 15, 2018.

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
ARTG 308272
Class IIa
Diagnostic x-ray digital imaging conversion system
ARTG ID: 308272
Good Name: Shimadzu Medical Systems Oceania Pty Ltd - Diagnostic x-ray digital imaging conversion system
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Intended Purpose

A device is intended for use in the acquisition and process of radiographic images of human anatomy. It is intended to replace radiographic film/screen system in general-purpose diagnostic procedures.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
308272
Start Date
August 15, 2018
Effective Date
August 15, 2018
Manufacturer
Country
Japan
Address
1 Sakura-machi Hino-shi, TOKYO, 1918511