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Tube/mask breathing circuit connector, non-sterile, single-use

Access comprehensive regulatory information for Tube/mask breathing circuit connector, non-sterile, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Device Technologies Australia Pty Ltd, manufactured by Vadi Medical Technology Co Ltd Yangmei in Taiwan. The device registration started on May 16, 2022.

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 IIa
Class IIa
Tube/mask breathing circuit connector, non-sterile, single-use
Australia TGA ARTG Registered Device
Good Name: Device Technologies Australia Pty Ltd - Tube/mask breathing circuit connector, non-sterile, single-use
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Intended Purpose

A connector intended to provide connection between two devices in order to enable the delivery of respiratory gases to the patient.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
May 16, 2022
Effective Date
May 16, 2022
Manufacturer
Country
Taiwan
Address
No 198 Lane 298 Huandong Road, ZhongShan Village Yangmei District, Taoyuan City, 32665