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Konica AeroDR - Diagnostic x-ray digital imaging conversion system - ARTG 460513

Access comprehensive regulatory information for Konica AeroDR - 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 460513 and sponsored by InMed Healthcare Pty Ltd, manufactured by Konica Minolta Inc in Japan. The device registration started on August 23, 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
ARTG 460513
Class IIa
Konica AeroDR - Diagnostic x-ray digital imaging conversion system
ARTG ID: 460513
Good Name: InMed Healthcare Pty Ltd - Konica AeroDR - Diagnostic x-ray digital imaging conversion system
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Intended Purpose

The flat panel sensor system is intended for healthcare professionals to capture for display radiographic images of human anatomy. It is intended for use in general projection radiographic applications wherever conventional film/screen or CR systems may be used. The device is not intended for mammography, fluoroscopy, tomography and angiography applications.

Device Classification
Risk Class
Class IIa
Product Type
Medical device system
ARTG Category
General
Registration Information
ARTG ID
460513
Start Date
August 23, 2024
Effective Date
August 23, 2024
Manufacturer
Country
Japan
Address
1 Sakura-machi Hino-shi, TOKYO, 1918511