Australia TGA ARTG record

Oximeter, pulse

Australia TGA ARTG Registered Device · YES Medical · Shenzhen Aeon Technology Co Ltd · Class IIa · Started August 20, 2021

Good Name: YES Medical - Oximeter, pulse

Device classification

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

Registration information

Start Date: August 20, 2021
Effective Date: August 20, 2021

Sponsor

Name: YES Medical

Manufacturer

Name: Shenzhen Aeon Technology Co Ltd
Country: China
Address: RM6H02 Block 27-29 Tianxia IC Industrial Park Majialong No 133 of Yiyuan Road, Nantou Street, Nanshan District Shenzhen, 518052

Intended purpose

A digital fingertip pulse oximeter intended for noninvasive spot-check measurement of SpO2 and pulse rate. The product is suitable for use in clinics and hospitals including clinical use in out-patient, casualty units, Day procedures etc.

About this record

Access comprehensive regulatory information for Oximeter, pulse in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by YES Medical, manufactured by Shenzhen Aeon Technology Co Ltd in China. The device registration started on August 20, 2021.

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.