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Bite registration device, <specify> - ARTG 390538

Access comprehensive regulatory information for Bite registration device, <specify> in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 390538 and sponsored by Wishmed Pty Ltd, manufactured by Premium Plus Japan Co Ltd in Japan. The device registration started on June 16, 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 I
ARTG 390538
Class I
Bite registration device, <specify>
ARTG ID: 390538
Good Name: Wishmed Pty Ltd - Bite registration device, <specify>
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Intended Purpose

Bite registration device is intended to be used during dental treatment for registration of the position of lower and upper jaws. It is a single use product.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
390538
Start Date
June 16, 2022
Effective Date
June 16, 2022
Sponsor
Manufacturer
Country
Japan
Address
2nd Floor 1-4-2 Jonan Ikedashi, Osaka, 5630025