Australia TGA ARTG recordGel, electrode
Australia TGA ARTG Registered Device · Seer Medical Holdings Ltd · Seer Medical Holdings Ltd · Class I · Started October 14, 2021
Good Name: Seer Medical Pty Ltd - Gel, electrode
- Risk Class
- Class I
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- October 14, 2021
- Effective Date
- October 14, 2021
- Country
- Australia
- Address
- 278 Queensberry Street, Melbourne, VIC, 3000
The Electrode Refill Gel is to supplement the existing electrical coupling gel under the recording electrodes for Neurophysiology examinations such as EEG studies.
Access comprehensive regulatory information for Gel, electrode in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by Seer Medical Holdings Ltd, manufactured by Seer Medical Holdings Ltd in Australia. The device registration started on October 14, 2021.
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.