Australia TGA ARTG recordTranscutaneous electrical stimulation electrode, reusable
Australia TGA ARTG Registered Device · Otto Bock Australia Pty Ltd · Bioness Inc · Class I · Started February 13, 2024
Good Name: Otto Bock Australia Pty Ltd - Transcutaneous electrical stimulation electrode, reusable
- Risk Class
- Class I
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- February 13, 2024
- Effective Date
- February 13, 2024
- Name
- Bioness Inc
- Country
- United States of America
- Address
- 25103 Rye Canyon Loop, Valencia, CA, 91355
An electrical conductor intended to be attached to the patient's skin to provide therapeutic electrical stimulate the body surface for for example transcutaneous electrical nerve stimulation ,electrical muscle stimulation.
Access comprehensive regulatory information for Transcutaneous electrical stimulation electrode, reusable in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by Otto Bock Australia Pty Ltd, manufactured by Bioness Inc in United States of America. The device registration started on February 13, 2024.
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.