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Connector, <specify> - ARTG 445953

Access comprehensive regulatory information for Connector, <specify> in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 445953 and sponsored by Air Liquide Healthcare Pty Ltd, manufactured by INOSYSTEMS SA in France. The device registration started on April 19, 2024.

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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Class I
ARTG 445953
Class I
Connector, <specify>
ARTG ID: 445953
Good Name: Air Liquide Healthcare Pty Ltd - Connector, <specify>
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Intended Purpose

Intended for sampling the inhaled gas during inhaled Nitric Oxide therapy with the Nitric Oxide delivery and monitoring system

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
445953
Start Date
April 19, 2024
Effective Date
April 19, 2024
Manufacturer
Country
France
Address
7 rue Georges Besse, Antony, 92160