Australia TGA ARTG record

Cuff, blood pressure, reusable

Australia TGA ARTG Registered Device · Philips Electronics Australia Ltd · SunTech Medical Inc · Class I · Started June 03, 2019

Good Name: Philips Electronics Australia Ltd - Cuff, blood pressure, reusable

Device classification

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

Registration information

Start Date: June 03, 2019
Effective Date: June 03, 2019

Sponsor

Name: Philips Electronics Australia Ltd

Manufacturer

Name: SunTech Medical Inc
Country: United States of America
Address: Suite 117 507 Airport Boulevard, Morrisville, NC, 27560-8200

Intended purpose

Indicated for blood pressure monitoring in patients from neonate to adult.

About this record

Access comprehensive regulatory information for Cuff, blood pressure, reusable in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by Philips Electronics Australia Ltd, manufactured by SunTech Medical Inc in United States of America. The device registration started on June 03, 2019.

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.