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Transcutaneous electrical stimulation electrode, reusable

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 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.

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Class I
Class I
Transcutaneous electrical stimulation electrode, reusable
Australia TGA ARTG Registered Device
Good Name: Boian Surgical Pty Ltd - Transcutaneous electrical stimulation electrode, reusable
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DJ Fang

DJ Fang

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Intended Purpose

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.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
March 19, 2024
Effective Date
March 19, 2024
Manufacturer
Country
China
Address
4/F No 1 TianShiDa Industrial Park No 79 Longwo Road Kengzi Street, Pingshan New District, Shenzhen, Guangdong Province