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Stimulator, electrical, analgesic, peripheral nerve, transcutaneous - ARTG 224675

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 registered under ARTG number 224675 and 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.

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TGA ARTG Official Data
Class IIa
ARTG 224675
Class IIa
Stimulator, electrical, analgesic, peripheral nerve, transcutaneous
ARTG ID: 224675
Good Name: Boian Surgical Pty Ltd - Stimulator, electrical, analgesic, peripheral nerve, transcutaneous
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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.

Device Classification
Risk Class
Class IIa
Product Type
Medical device system
ARTG Category
General
Registration Information
ARTG ID
224675
Start Date
June 18, 2014
Effective Date
June 18, 2014
Manufacturer
Country
Taiwan
Address
1F No 16 Lane 454 Jungjeng Road, Yunghe District, New Taipei City