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Philip​s EV300​

Important Notice

*In response to the August 2021 FDA​​ Class 2 Device Recall of the Trilogy EV300​, ​the SNS recovere​d and/or replaced all Philips Trilogy EV300 ventilator models deployed to U.S. health jurisdictions for COVID-19. SNS is coordinating closely with federal and commercial partners to resolve the recall issue.

The Trilogy EV300 ventilator delive​rs enhanced performance in noninvasive (NIV) and invasive (IV) ventilation, so patients can be treated with a single device throughout their hospital stay, regardless of changing conditions.

Fact Sheet
Trilogy EV300 Brochure


 Clinical Presentation