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Hi Scan - Digital imaging system, computed radiography, dental - ARTG 392039

Access comprehensive regulatory information for Hi Scan - Digital imaging system, computed radiography, dental in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 392039 and sponsored by Anthos In Australia, manufactured by Cefla SC in Italy. The device registration started on July 11, 2022.

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 392039
Class IIa
Hi Scan - Digital imaging system, computed radiography, dental
ARTG ID: 392039
Good Name: Anthos In Australia - Hi Scan - Digital imaging system, computed radiography, dental
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Intended Purpose

the Hi-Scan is a Phosphor plate system for acquiring and processing intraoral digital images that can be used with all intraoral X-ray systems. In order to manage the intraoral images, it is essential to use a personal computer and an image viewer program. The hy-scan system was developed to simplify the process of acquiring and viewing intraoral images on a digital screenโ€

Device Classification
Risk Class
Class IIa
Product Type
Medical device system
ARTG Category
General
Registration Information
ARTG ID
392039
Start Date
July 11, 2022
Effective Date
July 11, 2022
Manufacturer
Country
Italy
Address
Via Bicocca 14/C, Imola BO, 40026