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Philips Respironics E30 Ventilaton Solution

E30

Ventilaton Solution

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As COVID-19 continues to spread globally, healthcare providers are working diligently to treat soaring numbers of patients at a time when there are too few ventilators to provide care. Philips is responding to this pressing global need by quickly scaling production of the new Philips Respironics E30 ventilator with the needs of healthcare workers and COVID-19 patients.

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Features
Easy to use

Quick set-up and simple operations allowing healthcare providers with a wide range of skill sets to treat and monitor patients.

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 noninvasively with example accessories that may be used, such as a full-face, non-vented (without integrated leak) mask, or helmet.2

Recommended circuit set-ups contain a bacterial/viral filter to minimize exposure for healthcare providers when used invasively or noninvasively with example accessories that may be used, such as a full-face, non-vented (without integrated leak) mask, or helmet.2
Oxygen delivery

Safe entrainment of oxygen (patient circuit up to 30 lpm / device inlet up to 60 lpm) to deliver high levels of inspired oxygen.

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.3

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.3
  • Emergency Use Authorization The Philips Respironics E30 Ventilator is provided globally for use under local emergency use authorizations, such as the FDA Emergency Use Authorization for ventilators, Health Canada Interim Order for use in relation
  • to COVID-19, and waiver of CE marking, which authorize its use for the duration of the COVID-19 public health emergency, unless terminated or revoked (after which the products may no longer be used). This device is not FDA cleared or approved.
  • 1 This use is subject to an emergency use authorization, such as FDA Emergency Use Authorization for Ventilators, Health Canada Interim Order for use in relation to COVID-19, and waiver of CE marking.
  • 2 These circuit set-ups and accessories are examples provided for information purposes only as not all have been validated for use with the Philips Respironics E30 Ventilator.
  • 3 With attachments.

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