Australia TGA ARTG record

Gel, ultrasonic coupling

Australia TGA ARTG Registered Device · Philips Electronics Australia Ltd · Parker Laboratories Inc · Class I · Started August 12, 2019

Good Name: Philips Electronics Australia Ltd - Gel, ultrasonic coupling

Device classification

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

Registration information

Start Date: August 12, 2019
Effective Date: August 12, 2019

Sponsor

Name: Philips Electronics Australia Ltd

Manufacturer

Name: Parker Laboratories Inc
Country: United States of America
Address: 286 Eldridge Road, Fairfield, New Jersey, 07004

Intended purpose

Are non-sterile, water-soluble and non-staining gels intended for external use only and are used with all commercially available ultrasound devices.

About this record

Access comprehensive regulatory information for Gel, ultrasonic coupling 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 Parker Laboratories Inc in United States of America. The device registration started on August 12, 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.