Australia flagARTG 259155

Medicine chamber spacer

ARTG ID: 259155 · Cipla Australia Pty Ltd · Cipla Limited · Class I · Started September 04, 2015

Good Name: Cipla Australia Pty Ltd - Medicine chamber spacer

Device classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration information
ARTG ID
259155
Start Date
September 04, 2015
Effective Date
September 04, 2015
Sponsor
Manufacturer
Country
India
Address
Cipla House Peninsula Business Park, Ganpatrao Kadam Marg, Lower Parel Mumbai, 400 013
Intended purpose

A device in the form of a small container that is placed between a metered dose inhaler (MDI) and the patient's mouth, to function as a reservoir into which an aerosol medication is dispensed in order to minimize delivery of large aerosolized particles. It is typically made of plastic materials and is in the form as a small tube-like container. By holding the drug(s) after aerosolization, this device reduces the direct delivery of large aerosolized particles which would otherwise deposit in the mouth and which are intended for the lower airways. This is a reusable device

About this record

Access comprehensive regulatory information for Medicine chamber spacer in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 259155 and sponsored by Cipla Australia Pty Ltd, manufactured by Cipla Limited in India. The device registration started on September 04, 2015.

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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