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Electrode, transcutaneous, electrical nerve stimulation - ARTG 396783

Access comprehensive regulatory information for Electrode, transcutaneous, electrical nerve stimulation in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 396783 and sponsored by Veratemp, manufactured by Hivox Biotek Inc in Taiwan. The device registration started on September 30, 2022.

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 I
ARTG 396783
Class I
Electrode, transcutaneous, electrical nerve stimulation
ARTG ID: 396783
Good Name: Veratemp - Electrode, transcutaneous, electrical nerve stimulation
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Intended Purpose

Replacement electrical stimulation Gel-Pads for PAINmate TENS device.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
396783
Start Date
September 30, 2022
Effective Date
September 30, 2022
Sponsor
Manufacturer
Country
Taiwan
Address
5FNo 123 Shingde Road, Sanchong Dist., NewTaipei City, 241