ARTG 384972Transducer assembly, ultrasound, diagnostic, intracorporeal, vaginal
ARTG ID: 384972 · Olympus Australia Pty Ltd · FUJIFILM Healthcare Corporation · Class IIa · Started March 02, 2022
Good Name: Olympus Australia Pty Ltd - Transducer assembly, ultrasound, diagnostic, intracorporeal, vaginal
- Risk Class
- Class IIa
- Product Type
- Single Device Product
- ARTG Category
- General
- ARTG ID
- 384972
- Start Date
- March 02, 2022
- Effective Date
- March 02, 2022
- Country
- Japan
- Address
- 2-1 Shintoyofuta Kashiwa-shi, Chiba, 277-0804
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.
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.