Deep-tissue electromagnetic stimulation system, professional
Australia TGA ARTG Registered Device · MediCel Aesthetics · Zhengzhou PZ Laser Slim Technology Co Ltd · Class I · Started December 15, 2021
Good Name: MediCel Aesthetics - Deep-tissue electromagnetic stimulation system, professional
- Risk Class
- Class I
- Product Type
- Single Device Product
- ARTG Category
- General-Export
- Start Date
- December 15, 2021
- Effective Date
- December 15, 2021
- Country
- China
- Address
- Room 201 2nd Floor Building 2 No 52 Hongsong Road High-tech Development Zone, Zhengzhou City, Henan Province, 450001
Device for (EM) Electromagnetic Therapy. It is a device used for muscle strengthening and contouring using Functional Magnetic Stimulation
Access comprehensive regulatory information for Deep-tissue electromagnetic stimulation system, professional in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by MediCel Aesthetics, manufactured by Zhengzhou PZ Laser Slim Technology Co Ltd in China. The device registration started on December 15, 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.