ARTG 443974Transcutaneous electrical stimulation electrode, reusable
ARTG ID: 443974 · Boian Surgical Pty Ltd · Shenzhen Xingyuanli Technology Co Ltd · Class I · Started March 19, 2024
Good Name: Boian Surgical Pty Ltd - Transcutaneous electrical stimulation electrode, reusable
- Risk Class
- Class I
- Product Type
- Single Device Product
- ARTG Category
- General
- ARTG ID
- 443974
- Start Date
- March 19, 2024
- Effective Date
- March 19, 2024
- Country
- China
- Address
- 4/F No 1 TianShiDa Industrial Park No 79 Longwo Road Kengzi Street, Pingshan New District, Shenzhen, Guangdong Province
A non-invasive flexible, conductive pad intended, to be adhered to a patient's skin, to provide therapeutic electrical stimuli through the body surface [e.g., transcutaneous electrical nerve stimulation (TENS) or electrical muscle stimulation (EMS). This is a reusable device.
Access comprehensive regulatory information for Transcutaneous electrical stimulation electrode, reusable in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 443974 and sponsored by Boian Surgical Pty Ltd, manufactured by Shenzhen Xingyuanli Technology Co Ltd in China. The device registration started on March 19, 2024.
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.