Australia TGA ARTG record

Probe, <specify>

Australia TGA ARTG Registered Device · Baxter Healthcare Pty Ltd · Cheetah Medical Israel Ltd · Class I · Started May 30, 2020

Good Name: Baxter Healthcare Pty Ltd - Probe, <specify>

Device classification

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

Registration information

Start Date: May 30, 2020
Effective Date: May 30, 2020

Sponsor

Name: Baxter Healthcare Pty Ltd

Manufacturer

Name: Cheetah Medical Israel Ltd
Country: Israel
Address: 2A Hashlosha St F-32, Tel Aviv, Israel, 6706055

Intended purpose

Four non-invasive sensor pads are applied to the thorax, creating a “box” around the heart. A small electric current is applied across the thorax between the outer pair of sensors. A voltage signal is recorded between the inner pair of sensors. They do not have a monitoring function.

About this record

Access comprehensive regulatory information for Probe, <specify> in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by Baxter Healthcare Pty Ltd, manufactured by Cheetah Medical Israel Ltd in Israel. The device registration started on May 30, 2020.

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.