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Cuff, blood pressure, reusable - ARTG 318240

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 registered under ARTG number 318240 and 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.

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TGA ARTG Official Data
Class I
ARTG 318240
Class I
Cuff, blood pressure, reusable
ARTG ID: 318240
Good Name: Philips Electronics Australia Ltd - Cuff, blood pressure, reusable
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Intended Purpose

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

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
318240
Start Date
June 03, 2019
Effective Date
June 03, 2019
Manufacturer
Country
United States of America
Address
Suite 117 507 Airport Boulevard, Morrisville, NC, 27560-8200