Australia TGA ARTG record

CA-MI HI-FLO kit - Tubing set, nebulizer

Australia TGA ARTG Registered Device · Device Technologies Australia Pty Ltd · Ca-Mi Srl · Class IIa · Started October 29, 2019

Good Name: Device Technologies Australia Pty Ltd - CA-MI HI-FLO kit - Tubing set, nebulizer

Device classification

Risk Class: Class IIa
Product Type: Medical device system
ARTG Category: General

Registration information

Start Date: October 29, 2019
Effective Date: October 29, 2019

Sponsor

Name: Device Technologies Australia Pty Ltd

Manufacturer

Name: Ca-Mi Srl
Country: Italy
Address: Via Ugo La Malfa 13 Frazione Pilastro, Langhirano , PR, 43013

Intended purpose

A set of devices used to function in conjunction with a nebulizer/aerosol drug delivery device.

About this record

Access comprehensive regulatory information for CA-MI HI-FLO kit - Tubing set, nebulizer 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 Ca-Mi Srl in Italy. The device registration started on October 29, 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.