Australia TGA ARTG record

Connector, breathing circuit, reuseable

Australia TGA ARTG Registered Device · Innervate Pty Ltd · Hans Rudolph Inc · Class IIa · Started March 02, 2022

Good Name: Innervate Pty Ltd - Connector, breathing circuit, reuseable

Device classification

Risk Class: Class IIa
Product Type: Single Device Product
ARTG Category: General

Registration information

Start Date: March 02, 2022
Effective Date: March 02, 2022

Sponsor

Name: Innervate Pty Ltd

Manufacturer

Name: Hans Rudolph Inc
Country: United States of America
Address: 8325 Cole Parkway, Shawnee, KS, 66227

Intended purpose

A non-sterile device intended to connect a breathing circuit breathing tube to an endotracheal (ET) tube, anaesthesia face mask, or other non-sampling breathing circuit component. It is constructed with standardised connecting dimensions and may be designed to connect breathing tubes from paediatric to adult sizes. It may be made of plastic and/or metal and can have a straight or elbow-shaped design (excluding Y-piece connectors). Some designs may allow for partial rotation at the point of connection (a swivel) and may include a suction port or gas sampling port. This is a reusable device.

About this record

Access comprehensive regulatory information for Connector, breathing circuit, reuseable in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Innervate Pty Ltd, manufactured by Hans Rudolph Inc in United States of America. The device registration started on March 02, 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.