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
- Risk Class
- Class I
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- March 09, 2022
- Effective Date
- March 09, 2022
- Name
- Tenscare Limited
- Country
- United Kingdom
- Address
- PainAway House 9 Blenheim Road Longmead Business Park, Epsom, Surrey, KT19 9BE
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.
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.