Pure Global

Electrode, electrocardiograph, single use

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.

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TGA ARTG Official Data
Class I
Class I
Electrode, electrocardiograph, single use
Australia TGA ARTG Registered Device
Good Name: Cardio-Jenic Pty Ltd - Electrode, electrocardiograph, single use
Pure Global
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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.

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
Manufacturer
Country
United States of America
Address
550 Reserve Street Suite 360, Southlake, Texas, 76092