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Gel, ultrasonic coupling

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.

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TGA ARTG Official Data
Class I
Class I
Gel, ultrasonic coupling
Australia TGA ARTG Registered Device
Good Name: Philips Electronics Australia Ltd - Gel, ultrasonic coupling
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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.

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
Manufacturer
Country
United States of America
Address
286 Eldridge Road, Fairfield, New Jersey, 07004