Australia TGA ARTG recordSpirometer/pulmonary function analyser syringe
Australia TGA ARTG Registered Device · MGC Diagnostics Australia Pty Ltd · Hans Rudolph Inc · Class I · Started March 22, 2021
Good Name: MGC Diagnostics Australia Pty Ltd - Spirometer/pulmonary function analyser syringe
- Risk Class
- Class I
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- March 22, 2021
- Effective Date
- March 22, 2021
- Name
- Hans Rudolph Inc
- Country
- United States of America
- Address
- 8325 Cole Parkway, Shawnee, KS, 66227
This device is designed for testing and calibrating Flow and Volume Measurement Devices by injecting small volumes of gas into a spirometer, pulmonary function analyser, or other diagnostic pulmonary testing device for calibration or reference. This device is used by persons trained in the calibration procedures of the equipment under test. This is a reusable device.
Access comprehensive regulatory information for Spirometer/pulmonary function analyser syringe in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by MGC Diagnostics Australia Pty Ltd, manufactured by Hans Rudolph Inc in United States of America. The device registration started on March 22, 2021.
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.