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

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.

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TGA ARTG Official Data
Class IIa
Class IIa
CA-MI HI-FLO kit - Tubing set, nebulizer
Australia TGA ARTG Registered Device
Good Name: Device Technologies Australia Pty Ltd - CA-MI HI-FLO kit - Tubing set, nebulizer
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Intended Purpose

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

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
Manufacturer
Country
Italy
Address
Via Ugo La Malfa 13 Frazione Pilastro, Langhirano , PR, 43013