A readily available ventilator for both invasice and non-invasive use that fills the critical hospital ventilation shortage. The Philips Respironics E30 ventilator is authorized for use to treat patients with respiratory insufficiency.
Healthcare providers are working diligently to treat soaring numbers of patients at a time when there are too few ventilators to provide care.
VieMed is responding to this pressing global need by quickly distributing the
new Philips Respironics E30 ventilator with the needs of healthcare workers and patients in mind while also complying to medical device quality standards.
This global ventilator solution, can be purchased by governments and hospitals who are experiencing ventilator shortages. The Philips Respironics E30 ventilator can be used when there is limited access to a fully featured critical care ventilator.
Designed for mass production by a team deeply experienced in respiratory care, the Philips Respironics E30 ventilator meets numerous important needs.
FEATURES AND BENEFITS:
Easy to use
Quick set-up and simple operations allowing
healthcare providers with a wide range of skill sets
to treat and monitor patients.
Designed for your safety
Recommended circuit set-ups contain a bacterial/viral filter to minimize exposure for healthcare providers when used invasively or with example accessories that may be used, such as a full-face, non-vented (without integrated leak) mask, or helmet.
Safe entrainment of oxygen (patient circuit up to
30 lpm / device inlet up to 60 lpm) to deliver high
levels of inspired oxygen.
Key monitoring and alarms
On-screen respiratory monitoring (pressure, tidal
volume, RR, Minute Ventilation, leak and SpO2) as
well as visual and audible alarms to provide
pertinent therapy information.
FDA Emergency Use Authorization:
The Philips Respironics E30 Ventilator is provided globally under the Emergency Use Authorization issued by the US FDA for ventilators, ventilator tubing connectors and ventilator accessories, which authorizes its use for the duration of the US Health and Human Services public health emergency declaration justifying emergency use of these devices, unless terminated or revoked (after which the products may no longer be used). This device is not FDA cleared or approved.
Not for personal use. U.S. federal law restricts these devices to sale by or on the order of a physician.