Australia TGA ARTG recordWart-removal material
Australia TGA ARTG Registered Device · LaCorium Health Australia Pty Ltd · Logikal Health Products Pty Ltd · Class IIa · Started July 13, 2023
Good Name: LaCorium Health Australia Pty Ltd - Wart-removal material
- Risk Class
- Class IIa
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- July 13, 2023
- Effective Date
- July 13, 2023
- Country
- Australia
- Address
- Unit 3 18-20 Accolade Avenue, MORISSET, NSW, 2264
A non-sterile topical device intended to be applied to the surface of a wart for its eventual removal after repeated applications by dehydrating and drying warts. The precision of application with this intended device ensures controlled release of the formic acid onto the treatment site. It is normally available (non-prescription) over the counter (OTC). Application of formic acid in a unique precise applicator ensures that the intended device stays on the site of action and doesn’t harm the intact skin around the wart. After application, this device cannot be reused, although the product within the tube allows multiple application, within expiry date.
Access comprehensive regulatory information for Wart-removal material in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by LaCorium Health Australia Pty Ltd, manufactured by Logikal Health Products Pty Ltd in Australia. The device registration started on July 13, 2023.
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.