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Condensate trap, general-purpose, single use - ARTG 472025

Access comprehensive regulatory information for Condensate trap, general-purpose, single use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 472025 and sponsored by GE Healthcare Australia Pty Ltd, manufactured by GE Healthcare Finland Oy in Finland. The device registration started on December 06, 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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TGA ARTG Official Data
Class I
ARTG 472025
Class I
Condensate trap, general-purpose, single use
ARTG ID: 472025
Good Name: GE Healthcare Australia Pty Ltd - Condensate trap, general-purpose, single use
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Intended Purpose

This device is a water trap which is intended to be used with sidestream sampling and helps to protect GE monitors from water, secretions, and bacterial contamination during gas monitoring in the OR or ICU environments. The accessories are indicated for use by qualified medical personnel only. It is intended to facilitate the periodical removal of the accumulated liquid which can be discarded without interruption of the ongoing treatment or process. This device is reusable after has been appropriately cleansed between uses.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
472025
Start Date
December 06, 2024
Effective Date
December 06, 2024
Manufacturer
Country
Finland
Address
Kuortaneenkatu 2, Helsinki, FI-00510