Australia TGA ARTG record

Stimulator, electrical, analgesic, peripheral nerve, transcutaneous

Australia TGA ARTG Registered Device · Boian Surgical Pty Ltd · Well-Life Healthcare Ltd · Class IIa · Started June 18, 2014

Good Name: Boian Surgical Pty Ltd - Stimulator, electrical, analgesic, peripheral nerve, transcutaneous

Device classification

Risk Class: Class IIa
Product Type: Medical device system
ARTG Category: General

Registration information

Start Date: June 18, 2014
Effective Date: June 18, 2014

Sponsor

Name: Boian Surgical Pty Ltd

Manufacturer

Name: Well-Life Healthcare Ltd
Country: Taiwan
Address: 1F No 16 Lane 454 Jungjeng Road, Yunghe District, New Taipei City

Intended purpose

To treat pain associated with sore and aching muscles due to daily activities, surgery, trauma, musculoskeletal problems, bursitis or dental problems. It may also used in physical therapy.

About this record

Access comprehensive regulatory information for Stimulator, electrical, analgesic, peripheral nerve, transcutaneous in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Boian Surgical Pty Ltd, manufactured by Well-Life Healthcare Ltd in Taiwan. The device registration started on June 18, 2014.

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.