Australia TGA ARTG record

Hand-held deep-tissue electromagnetic stimulator

Australia TGA ARTG Registered Device · Evomed Pty Ltd · Bioelectronics Corporation · Class IIa · Started January 20, 2016

Good Name: Evomed Pty Ltd - Hand-held deep-tissue electromagnetic stimulator

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

Name: Evomed Pty Ltd

Manufacturer

Name: Bioelectronics Corporation
Country: United States of America
Address: 4539 Metropolitan Court, Frederick, MD, 21704

Intended purpose

ActiPatch uses Electromagnetic Pulse Therapy to relieve pain and inflammation.

About this record

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.