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Hand-held deep-tissue electromagnetic stimulator

Access comprehensive regulatory information for Hand-held deep-tissue electromagnetic stimulator in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Evomed Pty Ltd, manufactured by Bioelectronics Corporation in United States of America. The device registration started on January 20, 2016.

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.

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TGA ARTG Official Data
Class IIa
Class IIa
Hand-held deep-tissue electromagnetic stimulator
Australia TGA ARTG Registered Device
Good Name: Evomed Pty Ltd - Hand-held deep-tissue electromagnetic stimulator
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Intended Purpose

ActiPatch uses Electromagnetic Pulse Therapy to relieve pain and inflammation.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
January 20, 2016
Effective Date
January 20, 2016
Sponsor
Manufacturer
Country
United States of America
Address
4539 Metropolitan Court, Frederick, MD, 21704