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Endotherapy needle, single use - ARTG 445734

Access comprehensive regulatory information for Endotherapy needle, single use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 445734 and sponsored by Fujifilm Australia Pty Ltd, manufactured by FUJIFILM medwork GmbH in Germany. The device registration started on April 15, 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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TGA ARTG Official Data
Class IIa
ARTG 445734
Class IIa
Endotherapy needle, single use
ARTG ID: 445734
Good Name: Fujifilm Australia Pty Ltd - Endotherapy needle, single use
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Intended Purpose

The device is used for endoscopic injection in the upper and lower gastrointestinal tract.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
445734
Start Date
April 15, 2024
Effective Date
April 15, 2024
Manufacturer
Country
Germany
Address
Medworkring 1, Hochstadt, 91315