ARTG 461917Rectal/vaginal ultrasound imaging transducer
ARTG ID: 461917 · Fujifilm Australia Pty Ltd · Fujifilm Corporation · Class IIa · Started September 03, 2024
Good Name: Fujifilm Australia Pty Ltd - Rectal/vaginal ultrasound imaging transducer
- Risk Class
- Class IIa
- Product Type
- Single Device Product
- ARTG Category
- General
- ARTG ID
- 461917
- Start Date
- September 03, 2024
- Effective Date
- September 03, 2024
- Country
- Japan
- Address
- 26-30 Nishiazabu 2 Chome, MINATO KU TOKYO, 106 8620
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.
Access comprehensive regulatory information for Rectal/vaginal ultrasound imaging transducer in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 461917 and sponsored by Fujifilm Australia Pty Ltd, manufactured by Fujifilm Corporation in Japan. The device registration started on September 03, 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.