Australia flagARTG 227187

Stimulator, electrical, analgesic, peripheral nerve, transcutaneous

ARTG ID: 227187 · Veratemp · Hivox Biotek Inc · Class IIa · Started August 22, 2014

Good Name: Veratemp - Stimulator, electrical, analgesic, peripheral nerve, transcutaneous

Device classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration information
ARTG ID
227187
Start Date
August 22, 2014
Effective Date
August 22, 2014
Sponsor
Manufacturer
Country
Taiwan
Address
8F 98 Shinghe Road, Sanchong City, Taipei Hsien, 241
Intended purpose

A Transcutaneous Electrical Nerve Stimulation (TENS) device that emits controlled micro-electric impulses through the skin to interact with nerves for temporary pain relief. The pain relieving effect comes from blocking the nerve pathway transmitting pain signals.

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 registered under ARTG number 227187 and sponsored by Veratemp, manufactured by Hivox Biotek Inc in Taiwan. The device registration started on August 22, 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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