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Electrode, transcutaneous, electrical nerve stimulation - ARTG 385291

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 385291 and sponsored by Compliance Management Solutions, manufactured by Tenscare Limited in United Kingdom. The device registration started on March 09, 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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Class I
ARTG 385291
Class I
Electrode, transcutaneous, electrical nerve stimulation
ARTG ID: 385291
Good Name: Compliance Management Solutions - Electrode, transcutaneous, electrical nerve stimulation
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Intended Purpose

The QALM transcutaneous electrical nerve stimulation pads is an electrode that is designed to be placed on the patient's skin in order to deliver an electrical stimulus to reduce or eliminate pain.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
385291
Start Date
March 09, 2022
Effective Date
March 09, 2022
Manufacturer
Country
United Kingdom
Address
PainAway House 9 Blenheim Road Longmead Business Park, Epsom, Surrey, KT19 9BE