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Endotherapy forceps, biopsy, flexible, single-use

Access comprehensive regulatory information for Endotherapy forceps, biopsy, flexible, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Fujifilm Australia Pty Ltd, manufactured by FUJIFILM medwork GmbH in Germany. The device registration started on April 16, 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
Class IIa
Endotherapy forceps, biopsy, flexible, single-use
Australia TGA ARTG Registered Device
Good Name: Fujifilm Australia Pty Ltd - Endotherapy forceps, biopsy, flexible, single-use
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Intended Purpose

The device is used for taking samples from the upper and lower intestinal tract and from the bronchial tract.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
April 16, 2024
Effective Date
April 16, 2024
Manufacturer
Country
Germany
Address
Medworkring 1, Hochstadt, 91315