ARTG 421501Electrode, transcutaneous, electrical nerve stimulation
ARTG ID: 421501 · OneX Medical Australia Pty Ltd · Tenscare Limited · Class I · Started September 08, 2023
Good Name: OneX Medical Australia Pty Ltd - Electrode, transcutaneous, electrical nerve stimulation
- Risk Class
- Class I
- Product Type
- Single Device Product
- ARTG Category
- General
- ARTG ID
- 421501
- Start Date
- September 08, 2023
- Effective Date
- September 08, 2023
- Name
- Tenscare Limited
- Country
- United Kingdom
- Address
- PainAway House 9 Blenheim Road Longmead Business Park, Epsom, Surrey, KT19 9BE
GMDN: 35995 These products are adhesive electrodes which are intended for use as the disposable, conductive adhesive interface between the patient’s skin and the Electrical Stimulator. They are intended to be used with marked Electrical Stimulators, i.e. TENS (Transcutaneous Electrical Nerve Stimulation) and EMS (Electrical Muscular Stimulation)
Access comprehensive regulatory information for Electrode, transcutaneous, electrical nerve stimulation in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 421501 and sponsored by OneX Medical Australia Pty Ltd, manufactured by Tenscare Limited in United Kingdom. The device registration started on September 08, 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.