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Electrode, transcutaneous, electrical nerve stimulation

Australia TGA ARTG Registered Device · Compliance Management Solutions · Tenscare Limited · Class I · Started March 09, 2022

Good Name: Compliance Management Solutions - Electrode, transcutaneous, electrical nerve stimulation

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

About this record

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 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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