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Transducer assembly, ultrasound, diagnostic, intracorporeal, vaginal - ARTG 384972

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 384972 and sponsored by Olympus Australia Pty Ltd, manufactured by FUJIFILM Healthcare Corporation in Japan. The device registration started on March 02, 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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TGA ARTG Official Data
Class IIa
ARTG 384972
Class IIa
Transducer assembly, ultrasound, diagnostic, intracorporeal, vaginal
ARTG ID: 384972
Good Name: Olympus Australia Pty Ltd - Transducer assembly, ultrasound, diagnostic, intracorporeal, vaginal
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Intended Purpose

This probe is intended for use by a doctor or other qualified operator for inserting into a human vagina and making ultrasonic observations of the uterus and surrounding organs.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
384972
Start Date
March 02, 2022
Effective Date
March 02, 2022
Manufacturer
Country
Japan
Address
2-1 Shintoyofuta Kashiwa-shi, Chiba, 277-0804