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Spirometer, diagnostic

Access comprehensive regulatory information for Spirometer, diagnostic in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Dalmedi Technologies Pty Ltd, manufactured by Beijing M&B Electronic Instruments Co Ltd in China. The device registration started on April 09, 2018.

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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Class IIa
Class IIa
Spirometer, diagnostic
Australia TGA ARTG Registered Device
Good Name: Dalmedi Technologies Pty Ltd - Spirometer, diagnostic
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Intended Purpose

Intended for monitoring peak expired flow rate (PEF) and forced expiratory volume in one second (FEV1).

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
April 09, 2018
Effective Date
April 09, 2018
Manufacturer
Country
China
Address
Rm 6319 Bldg 1 27 Yongwang Road Daxing Bioengineering and Medicine Industry Base, Zhongguancun Science Park, Daxing District Beijing, 102629