Australia TGA ARTG record

Electrode, electrocardiograph, single use

Australia TGA ARTG Registered Device · Cardio-Jenic Pty Ltd · Heart Test Laboratories Inc dba Heart Sciences · Class I · Started August 17, 2017

Good Name: Cardio-Jenic Pty Ltd - Electrode, electrocardiograph, single use

Device classification

Risk Class: Class I
Product Type: Single Device Product
ARTG Category: General

Registration information

Start Date: August 17, 2017
Effective Date: August 17, 2017

Sponsor

Name: Cardio-Jenic Pty Ltd

Manufacturer

Name: Heart Test Laboratories Inc dba Heart Sciences
Country: United States of America
Address: 550 Reserve Street Suite 360, Southlake, Texas, 76092

Intended purpose

The MyoVista Center Post Electrodes are a proprietary single-use disposable designed to provide consistent, high quality signal capture for exclusive use with MyoVista hsECG device.

About this record

Access comprehensive regulatory information for Electrode, electrocardiograph, single use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by Cardio-Jenic Pty Ltd, manufactured by Heart Test Laboratories Inc dba Heart Sciences in United States of America. The device registration started on August 17, 2017.

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.