PHARMAGAS: The First and Only CE MDR-Certified Medical Fluid Analyzer
Published on October 29, 2026
NOVAIR announces that it has obtained CE MDR certification for its PHARMAGAS device, a cabinet for analyzing the quality of medical fluids, in accordance with European Regulation (EU) 2017/745.
The PHARMAGAS is the first and only analysis cabinet of its kind to receive this certification.
Classified as a Class IIb Medical Device, the PHARMAGAS meets the highest standards of quality and reliability. It provides continuous monitoring of the quality of oxygen and medical air distributed throughout hospital networks.
With its modular design, it analyzes up to 8 quality parameters: CO and COâ‚‚ as standard, plus Hâ‚‚O, Oâ‚‚, NO, NOâ‚‚, SOâ‚‚, and OIL using additional modules. It provides real-time monitoring, with visual alarms if defined thresholds are exceeded, and records measurements to facilitate quality tracking of medical fluids.
This certification, issued by DNV, is the result of the work of NOVAIR’s Quality & Regulatory Affairs and Engineering/Design teams. With PHARMAGAS, NOVAIR is setting a new standard for monitoring the quality of medical fluids, ensuring the safety of healthcare facilities and patients.