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Rectal/vaginal ultrasound imaging transducer - ARTG 461917

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.

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Class IIa
ARTG 461917
Class IIa
Rectal/vaginal ultrasound imaging transducer
ARTG ID: 461917
Good Name: Fujifilm Australia Pty Ltd - Rectal/vaginal ultrasound imaging transducer
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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
461917
Start Date
September 03, 2024
Effective Date
September 03, 2024
Manufacturer
Country
Japan
Address
26-30 Nishiazabu 2 Chome, MINATO KU TOKYO, 106 8620