Australia TGA ARTG recordElectrode, transcutaneous, electrical nerve stimulation
Australia TGA ARTG Registered Device · Veratemp · Hivox Biotek Inc · Class I · Started September 30, 2022
Good Name: Veratemp - Electrode, transcutaneous, electrical nerve stimulation
- Risk Class
- Class I
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- September 30, 2022
- Effective Date
- September 30, 2022
- Name
- Veratemp
- Name
- Hivox Biotek Inc
- Country
- Taiwan
- Address
- 5FNo 123 Shingde Road, Sanchong Dist., NewTaipei City, 241
Replacement electrical stimulation Gel-Pads for PAINmate TENS device.
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 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.