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Transducer assembly, ultrasound, diagnostic, intracorporeal, vaginal - ARTG 378300

Access comprehensive regulatory information for Transducer assembly, ultrasound, diagnostic, intracorporeal, vaginal in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 378300 and sponsored by Fujifilm Australia Pty Ltd, manufactured by FUJIFILM Healthcare Corporation in Japan. The device registration started on November 19, 2021.

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 378300
Class IIa
Transducer assembly, ultrasound, diagnostic, intracorporeal, vaginal
ARTG ID: 378300
Good Name: Fujifilm Australia Pty Ltd - Transducer assembly, ultrasound, diagnostic, intracorporeal, vaginal
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Intended Purpose

The subject ultrasound imaging probes are intended to be positioned within the human vagina or rectum for making ultrasound observations of uterus, prostate and surrounding organs.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
378300
Start Date
November 19, 2021
Effective Date
November 19, 2021
Manufacturer
Country
Japan
Address
2-1 Shintoyofuta Kashiwa-shi, Chiba, 277-0804