V60 Plus Ventilator

V60 Plus

Ventilator

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Philips V60 Plus ventilator leverages our noninvasive (NIV) capabilities by offering two therapy options in one device, integrating both NIV and high flow therapy (HFT). V60 Plus enhances workflow and patient care efficiency by enabling clinicians to easily, readily and rapidly adjust therapies around changing patient conditions without switching devices.

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Features

Quick transition between NIV and HFT: Quick transition between NIV and HFT

With the combination of NIV and HFT modes on one device, the V60 Plus is essential in supporting rapid weaning. And because it is an all-in-one device, you can streamline your equipment and consumables inventory.
Advanced NIV with Auto-Trak technology: Advanced NIV with Auto-Trak technology

By providing auto-adaptive leak compensation, inspiratory triggering, and expiratory cycling, Auto-Trak delivers optimal synchrony in the face of dynamic leak and changing patient demand. Noninvasive ventilation modes and options include: S/T, AVAPS, PCV, CPAP with C-Flex, PPV and Auto-Trak Plus.
Save time with automatic mask calibration: Save time with automatic mask calibration

Pre-defined settings for Philips hospital masks help you save time when initiating treatment. You select the setting, and the V60 Plus automatically calibrates flow characteristics for better monitoring and therapy.
Flexible, easy, upgradeable: Flexible, easy, upgradeable

Designed to include pediatric use (20kg or greater) and equipped with several modes as well as HFT, the V60 Plus allows you to meet the specific needs of your patients. The high-resolution touchscreen makes operation easy and facilitates waveform interpretation. The internal six-hour battery enables intra-hospital transport.

* May not be available in all markets, please check with your Philips representative for complete portfolio availability.
Software version 3.00 is a modification to the existing V60 ventilator and is therefore provided for use in accordance with FDA’s recent guidance, Enforcement Policy for Ventilators and Accessories and Other Respiratory Devices During the Coronavirus Disease 2019 (COVID-19) Public Health Emergency, Section IV Policy for Modifications to FDA-Cleared Devices, issued March 2020. It is intended to remain in effect only for the duration of the public health emergency related to COVID-19 declared by the Department of Health and Human Services (HHS)