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Vyaire Medical Receives FDA Clearance of New Pulmonary Function Testing Technology

Tuesday, August 20, 2019 Respiratory Disease News
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Vyntus™ ONE, Vyntus™ BODY and SentrySuite™ Software Available to U.S. Healthcare Market Immediately

CHICAGO, Aug. 20, 2019 /PRNewswire/ -- Vyaire Medical, Inc., the healthcare industry's dedicated "breathing company," today announced the U.S. Food and Drug Administration (FDA) has granted FDA 510(k) clearance for two of its latest Pulmonary Function Testing (PFT) technologies: Vyntus ONE, Vyntus BODY with SentrySuite Software. 
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The Vyntus ONE is designed to be a convenient PFT station available in a fixed or mobile configuration that is patient-friendly and easy for clinicians to use. Vyntus BODY is engineered to conduct body plethysmography to measure lung capacity and other pulmonary functions for patients of all sizes and mobility, offering larger interior space to accommodate patients of any size without increasing the footprint of the cabin.  Both Vyntus ONE and Vyntus BODY include a newly designed Ultrasonic Flow Sensor that represents significant improvements in efficiency and accuracy of pulmonary function testing.
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All Vyntus technologies run on the SentrySuite Software, which is easy-to-operate and designed completely around the user experience for accurate results and optimal workflow. SentrySuite provides seamless integration and secure connectivity with both the clinical infrastructure and the electronic medical records (EMR) platform.

"These new Vyntus products offer a modern ergonomic design, state-of-the-art ultrasonic sensor technology for consistent and accurate respiratory testing as well as more efficient hygiene and maintenance protocols for customers," said Dave Eckley, Vyaire's Chief Executive Officer. "These benefits are absolutely meaningful in today's respiratory diagnostics clinical environment and demonstrate the value of the Vyaire technologies."

Vyaire believes this product launch represents the most progressive innovation in the Respiratory Diagnostics field in many years. Vyntus ONE and Vyntus BODY are the continued expansion of the portfolio – including Vyntus CPX, Vyntus SPIRO, Vyntus WALK, and Vyntus ECG – all of which run on the SentrySuite Software platform.

Learn more at vyaire.com

About Vyaire Medical Headquartered in Chicago, IL., Vyaire Medical supports and improves the lives of patients with an unyielding focus on improving patient outcomes and increasing value for customers. The company was formed in October 2016, to serve healthcare customers with innovative device and service solutions across the respiratory and anesthesia continua of care.  Vyaire's legacy brands have a 65-year track record of pioneering, innovating, and advancing respiratory diagnostics, ventilation, and anesthesia delivery & patient monitoring.

From industry-pioneering brands that include Bird, Bear, and Jaeger to respected industry leaders AirLife™, Vital Signs™, Viasys, and many others — Vyaire Medical has nearly 27,000 distinct part numbers recognized, trusted and preferred by specialists in the respiratory therapy and anesthesiology healthcare markets worldwide.

Learn more at www.vyaire.com.

NOTE TO EDITORS: Product photography and technical information available upon request.

For U.S. distribution. © 2019 Vyaire. Vyaire, the Vyaire logo and all other trademarks or registered trademarks are property of Vyaire Medical, Inc., or one of its affiliates. VYR-US-1800043

Contact Debra Goetz Chief Brand & Digital Officer Phone:  +1 (872)-221-7450 Email: [email protected]

Cision View original content:http://www.prnewswire.com/news-releases/vyaire-medical-receives-fda-clearance-of-new-pulmonary-function-testing-technology-300904013.html

SOURCE Vyaire Medical

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