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Endoscopic electrosurgical electrode/submucosal lift needle - ARTG 421913

Access comprehensive regulatory information for Endoscopic electrosurgical electrode/submucosal lift needle in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is registered under ARTG number 421913 and sponsored by Rymed Pty Ltd, manufactured by Erbe Elektromedizin GmbH in Germany. The device registration started on September 15, 2023.

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 IIb
ARTG 421913
Class IIb
Endoscopic electrosurgical electrode/submucosal lift needle
ARTG ID: 421913
Good Name: Rymed Pty Ltd - Endoscopic electrosurgical electrode/submucosal lift needle
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Intended Purpose

The Hybrid Knife flex is intended for monopolar cutting and coagulation, needle free injection and tissue selective hydro dissection including lifting mucosal lesions by injecting into the submucosa

Device Classification
Risk Class
Class IIb
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
421913
Start Date
September 15, 2023
Effective Date
September 15, 2023
Sponsor
Manufacturer
Country
Germany
Address
Waldhornlestrasse 17, Tubingen, Tubingen, 72072