ARTG 464251BIOFLEX MiniPort Home - Red-light phototherapy unit, home-use
ARTG ID: 464251 · RQSolutions Medical Devices Distribution Support · Meditech International Inc · Class IIa · Started October 14, 2024
Good Name: RQSolutions Medical Devices Distribution Support - BIOFLEX MiniPort Home - Red-light phototherapy unit, home-use
- Risk Class
- Class IIa
- Product Type
- Medical device system
- ARTG Category
- General
- ARTG ID
- 464251
- Start Date
- October 14, 2024
- Effective Date
- October 14, 2024
- Country
- Canada
- Address
- Unit 1/411 Horner Avenue, Toronto, Ontario, M8W 4W3
he BIOFLEX MiniPort Home is used by trained healthcare professionals as well as general public and is indicated for use to emit energy in the red and infrared spectrum to provide topical heating for the purpose of elevating tissue temperature for temporary relief of minor muscle and joint pain, arthritis, muscle spasm, relieving stiffness, promoting relaxation of muscle tissue and temporary increase in local blood circulation.
Access comprehensive regulatory information for BIOFLEX MiniPort Home - Red-light phototherapy unit, home-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 464251 and sponsored by RQSolutions Medical Devices Distribution Support, manufactured by Meditech International Inc in Canada. The device registration started on October 14, 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.