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Analgesic TENS system

Australia TGA ARTG Registered Device · Australian Physiotherapy Equipment · Everyway Medical Instruments Co Ltd · Class IIa · Started July 06, 2020

Good Name: Australian Physiotherapy Equipment - Analgesic TENS system

Device classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration information
Start Date
July 06, 2020
Effective Date
July 06, 2020
Sponsor
Manufacturer
Country
Taiwan
Address
3 Fl & 8 Fl No 5 Lane 155 Section 3 Bei-Sheng Road, Shenkeng District, New Taipei City, 22203
Intended purpose

Analgesic peripheral nerve stimulator consisting of external stimulator and electrode placed on the skin not penetrating the body at any time, so electrical stimulus is applied through the skin (transcutaneously) to the painful area. It typically includes several predetermined stimulation modulation options, e.g. pulse frequency or pulse duration. This device is also known as a transcutaneous electric nerve stimulator (TENS) and is used to treat pain associated with surgery, trauma, musculoskeletal problems, bursitis or dental problems. It is also used in physical therapy.

About this record

Access comprehensive regulatory information for Analgesic TENS system in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Australian Physiotherapy Equipment, manufactured by Everyway Medical Instruments Co Ltd in Taiwan. The device registration started on July 06, 2020.

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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