Trilogy Evo lets you smoothly transition patients through different care settings using the same clinical technologyfor continuous peace of mind. Digital Auto-Trak provides an automated breath triggering and cycling algorithm that adjusts to the patient's natural breathing patterns. The next generation of the Philips Trilogy ventilator delivers proven performance in noninvasive (NIV) and invasive (IV) ventilation, and is designed to stay with your patients across changing care environments. Auto Back-up Rate delays a machine breath until your patient exhales to maximize comfort. SpO2, EtCO2 and advanced respiratory mechanics monitoring capabilities are designed to help you optimize your patients therapy. Before sharing sensitive information, make sure you're on a federal government site. Portable Oxygen Concentrators and Accessories, Sleep Diagnostics Systems Accessories and Supplies, Trilogy Evo is the only industry-leading ventilator with 15 hours of battery life with an internal and detachable battery, Every Trilogy Evo is equipped to connect with Care Orchestrator, and you can download data wirelessly or via the USB port, Trilogy Evo has a four-year service interval. to-use carry bag. It's designed specifically with durability in mind to protect it against damage during travel, such as during medical transport. Flexibility of circuits allows it to be used in a wide range of patients. Koninklijke Philips N.V., 2004 - 2023. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. Nominal run time per method in International Electrotechnical Commission (7.5 hour/battery). Proven innovations are designed to treat the varying needs of respiratory insufficiency. There were no reports of patient injury or death among those 30 MDRs. If you have a health issue, including those listed under potential health risks below, or any problem with your device, talk to your health care provider and. The mouthpiece ventilation does not require any inspiratory effort in order to trigger a breath. The Amsterdam-based medical device company began a recall in March. Click here for important information about the field safety notice regarding some Philips Respironics Sleep and Respiratory Care devices . This is a 10-pack of particulate filters for use with the Trilogy Evo and Trilogy EV300 ventilators. All rights reserved. Digital Auto-Trak provides an automated breath triggering and cycling algorithm that adjusts to the patient's natural breathing patterns. If the lot number used in repair is between 210414 and 210524. The support, service and upkeep behind Trilogy Evo includes 24-hour clinical support, educational training resources for both you and your patients, and extended warranties and maintenance plans. Trilogy Evo provides noninvasive and invasive ventilator support with added sensitivity for a wide range of adult and pediatric patients. Trilogy Evo Trilogy Evo O2 Trilogy 100 Trilogy 200 Philips Hospital/Home Ventilation Solutions 1. Follow the recommendations above for the recalled devices used in health care settings. 2. *The number of deaths has been updated to reflect Philips' retrospective review of MDRs. A/C-VC modeActivePAPcircuit, PEEP 3cmH2O andVt800ml. 2. Contact us Specifications Contact us Request contact Specifications Can we help? It's very user-friendly as kind of a "mini V60" with simplicity in setting pressure and frequency, setting up patients or changing modes, but as powerful as a V60. to-use carry bag. Inline bacterial filters may increase the resistance to air flow through the device, which could mean the ventilator will not ventilate adequately. Volume and pressure modes, AVAPS-AE, SpO2 and EtCO2 monitoring and alarms of every parameter allow for adaptable care. You can also download data at the point of care through a USB drive. The Trilogy Evo is a portable hospital-to-home ventilator that is intuitive, easy to use, features a long-lasting battery and more! Additionally, after placement of an inline filter, instruct patients and/or caregivers to be aware of potential changes in breathing circuit resistance and monitor as ventilator performance may change due to increase in resistance of air flow through the device after filter placement. The .gov means its official.Federal government websites often end in .gov or .mil. This URGENT Field Safety Notice is intended to inform you of the problem. Trilogy Evo is intended for pediatric through adult patients weighing at least 2.5 kg. This ventilation parameters tool provides a quick and easy way to calculate IBW, inspiratory time and I:E ratios, This video will demonstrate how to set up the passive, activePAP, active flow and dual limb circuits for Trilogy Evo, This video will demonstrate how to initiate ventilation with Trilogy Evo, This video will demonstrate how to ventilate a patient and navigate through the various windows, This video will review some of the accessories compatible with Trilogy Evo, Trilogy Evo Quick Start Guide for clinicians, A clinician focused guide on transitioning to the Trilogy Evo platform. The Food and Drug Administration posted the recall to its database on Monday, designating it a Class I recall, the most . Click here for important information about the recall of certain Philips Respironics Sleep and Respiratory Care devices. You can also download data at the point of care through a USB drive. Read more in the safety communication for Certain Reworked Philips Respironics Trilogy 100/200 Ventilators Recalled Due to Potential for Silicone Foam Adhesion Failure and Residual PEPUR Foam Debris. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. A wide range of injuries have been reported in these MDRs, including cancer, pneumonia, asthma, other respiratory problems, infection, headache, cough, dyspnea (difficulty breathing), dizziness, nodules, and chest pain. Volume and pressure modes, AVAPS-AE, SpO2 and EtCO2 monitoring and alarms of every parameter allow for adaptable care. Auto Back-up Rate delays a machine breath until your patient exhales to maximize comfort. The Trilogy Evo was developed specifically for use in its respective environment. It offers new, on-screen Help and Alarm guidance and user-friendly universal names for most ventilation modes. Assure blankets are not covering the exhalation port/valve F:\Company Shared Folders\Respiratory\New Set Ups\Trilogy ventilator set up\forms\MASTER TEMPLATES\Miscellaneous\Trilogy Alarm Troubleshooting Guide 6-2019 Philips Respironics sent an Urgent Medical Device Recall notification to Trilogy Evo ventilator customers on December 21, 2021, and the company sent an updated version to clarify information on cleaning and filters on January 13, 2022. Code Information. AVAPS automatically adjusts the ventilator support to reach the desired tidal volume, while Auto EPAP proactively adjusts to the lowest effective pressure to manage the upper airway. Contact Philips for next steps. The e-learning videos and modules on this Trilogy Evo education curriculum are intended for self- learning and review how to set-up Trilogy Evo for ventilation. All Rights Reserved. By clicking on the link, you will be leaving the official Royal Philips ("Philips") website. Our site can best be viewed with the latest version of Microsoft Edge, Google Chrome or Firefox. The Trilogy Evo ventilator provides invasive and non-invasive, positive pressure ventilation to adult, pediatric, and infant patients with a minimum weight of 2.5 kg. The NKV-550 ventilator with Protective Control is the only critical care ventilator, at the time of this press release, that has received US FDA's 510(k) clearance for this feature, a review process more rigorous than the FDA's Emergency Use Authorization. Turn the Trilogy nebulizer feature to "on" 3. Trilogy Evo provides noninvasive and invasive ventilator support with added sensitivity for a wide range of adult and pediatric patients. Similar testing provided by Philips to the FDA on devices authorized for marketing in the U.S. had demonstrated acceptable results. Connect care teams across the continuum of care. By specifying your reason for contact we will be able to provide you with a better service. Proven innovations are designed to treat the varying needs of respiratory insufficiency. The FDA has identified this as a Class I recall, the most serious type of recall. Ventilator-dependent patients are supported by internal and detachable batteries, now with 15-hour battery life. Enquire with a Philips healthcare sales rep, Subscribe for regular news and updates from Philips, Get technical support for a healthcare product, Find product documentation and instructions for use, Synchronized intermittent mandatory ventilation (pressure control), Synchronized intermittent mandatory ventilation (volume control), Mouthpiece ventilation (pressure control), 16.5 cm D x 28.6 cm W x 24.5 cm H 6.48 D x 11.25 W x 9.65 H, 15 hours nominal total run time per method in IEC 80601-2-72 (7.5 hours each battery), from 0% to 80%: 2.5 hours; from 0% to 100%: 3.5 hours, 35 - 2000 ml on Dual Limb and Active Flow circuits, 50 - 2000 ml on passive and active PAP circuits, 0 - 35 cmH20 for active circuits 3 - 25 cmH20 for passive circuits, Off, AutoTrak, Sensitive, AutoTrak, and Flow Trigger. You will be shipped replacements. Philips issued a recall of its Trilogy Evo portable electric ventilators due to a problem with an internal sensor that can lead to under-delivery of oxygen. Quick links to help you find what you need or see how to get in touch with a customer service representative. Its designed specifically with durability in mind to protect it against damage during travel, such as during medical transport. Klink, the Philips spokesman, said the $13.8 million from HHS covered. Philips will replace the device these parts were installed into. The Trilogy Evo getting started interactive module contains knowledge checks throughout and a final assessment at the end which requires a score of 80% in order to obtain the learning certificate. With BARDA's continuing support, Philips finally won FDA approval for the Trilogy Evo Universal ventilator in July 2019. You are about to visit a Philips global content page. A team of engineers, scientists, and clinicians of Nihon Kohden OrangeMed Inc, the . Koninklijke Philips N.V., 2004 - 2023. Versatile breath delivery and setup options provide greater continuity of care. Medical Device Recalls, Recalls, Market Withdrawals and Safety Alerts, Philips Respironics Recalls Certain Trilogy EVO Ventilators for Potential Health Risks from PE-PUR Foam, Trilogy Evo ventilator model numbers with certain serial numbers, Repair kits for Trilogy Evo muffler assembly model and lot numbers, Potential Health Risks from Sound Abatement Foam, Update: Certain Philips Respironics Ventilators, BiPAP, and CPAP Machines Recalled Due to Potential Health Risks: FDA Safety Communication, Trilogy Evo, Material Numbers DS2110X11B (USA) and KR2110X15B (Korea), Trilogy Evo Repair Kit, RP-Trilogy Evo Muffler Assembly, Material Number 1135257, report adverse reactions or quality problems, Repair kits for Trilogy Evo muffler assembly*, Manufacturing Dates: April 15, 2021 to May 24, 2021, Distribution Dates: April 15, 2021 to May 24, 2021, Devices Recalled in the U.S.: 215 Trilogy Evo ventilators; 51 Trilogy Evo repair kits, Date Initiated by Firm: December 21, 2021, People using these devices and their caregivers, Durable Medical Equipment (DME) suppliers. Trilogy Evo is designed for easy navigation and fast set-up of prescriptions. The site is secure. Determine if any Trilogy Evo devices have been repaired using Trilogy Evo Muffler Assembly Part Number 1135357 starting 14 April 2021 or later. Trilogy Evo provides noninvasive and invasive ventilator support with added sensitivity for a wide range of adult and pediatric patients. Trilogy Evo is designed for easy navigation and fast set-up of prescriptions. You can also download data at the point of care through a USB drive. Trilogy Evo ventilators deliver enhanced performance in both non-invasive (NIV) and invasive ventilation. Compared to Trilogy 100s six-hour battery, Trilogy Evo gives patients a new level of freedom and mobility. The mouthpiece ventilation does not require any inspiratory effort in order to trigger a breath. Health care personnel employed by facilities that are subject to the FDA's user facility reporting requirements should follow the reporting procedures established by their facilities. If you have additional concerns, talk to your health care provider about the plan for your care and treatment. All rights reserved. Go digital and save time with signNow, the best solution for electronic signatures.Use its powerful functionality with a simple-to-use intuitive interface to fill out Trilogy100 Ventilator online, e-sign them, and quickly share them without jumping tabs. Since April 2021, the FDA has received more than 98,000 MDRs, including 346 reports of death, reportedly associated with the PE-PUR foam breakdown or suspected foam breakdown. By clicking on the link, you will be leaving the official Royal Philips ("Philips") website. A problem has been identified within the Philips Respironics Trilogy Evo 02, Trilogy Evo Universal, and Trilogy EV300 ventilators that could pose a risk for patients if not mitigated. Copyright 2023 Apria Healthcare Group LLC. The devices are used to help breathing. Invasive/non-invasive; portability for intra-hospital transport and hospital-to-home transition, Auto-adaptive technology can help patient synchrony and therapy acceptance, Up to six hours* of battery life supports portability, Bluetooth connectivity options along with optional SpO2 monitoring, Two circuit options for simple, flexible use, Passive circuit option for passive exhalation, Active with PAP circuit option supports proximal pressure sensing, Unify care teams and enhance interoperability. SpO2, EtCO2 and advanced respiratory mechanics monitoring capabilities are designed to help you optimize your patients therapy. The newest Trilogy device was made to be user-friendly without compromising the advanced features of the innovative Trilogy family technology. What is the Trilogy Evo Ventilator? The mouthpiece ventilation does not require any inspiratory effort in order to trigger a breath. From hospital to home or clinicians to caregivers, transitions in respiratory care can be challenging. Instruct patients and/or caregivers to closely monitor the bacteria filter for foam debris. The e-learning videos and modules on this Trilogy Evo education curriculum are intended for self- learning and review how to set-up Trilogy Evo for ventilation. With Care Orchestrator, you have the power to create custom health rules based on your best practices and proven processes. Trilogy Evo is designed for easy navigation and fast set-up of prescriptions. We are always interested in engaging with you. Features. Use another similar device that is not a part of this recall. You may or may not see black pieces of the foam in the air tubes or masks. The ventilator is suitable for use in institutional, home, and non-emergency transport settings, for example wheelchair or personal vehicle. Digital Auto-Trak provides an automated breath triggering and cycling algorithm that adjusts to the patients natural breathing patterns. Trilogy Evo has a four-year service interval. Trilogy Evo uses Bluetooth to send you patient and device data through Care Orchestrator, our cloud-based tool. The support, service and upkeep behind Trilogy Evo includes 24-hour clinical support, educational training resources for both you and your patients, and extended warranties and maintenance plans. A/C-VC modeActivePAPcircuit, PEEP 3cmH2O andVt800ml.. The U.S. Food and Drug Administration (FDA) is updating the June 2021 safety communication about the Philips Respironics (Philips) recalled ventilators, bilevel positive airway pressure (also known as Bilevel PAP, BiPAP, or BPAP) machines, and continuous positive airway pressure (CPAP) machines. Customers are instructed to: 1) Compare the serial numbers of their device(s) to Attachment A: List of . With Care Orchestrator, you have the power to create custom health rules based on your best practices and proven processes. The results from the independent testing are needed to determine if the silicone-based foam used in the repaired devices does in fact present any risks to patients. Trilogy 100 (ventilator) Trilogy 200 (ventilator) Philips also recalled certain Trilogy Evo ventilators distributed from April 15, 2021 to May 24, 2021 with specific serial numbers.. Increase your teams efficiencies and streamline your workflow for a sharper focus on higher clinical priorities. data fl ow, Trilogy Evo helps benefi t a broad spectrum of patients, from newborns to adults. The Philips Respironics Trilogy 202 is both a volume-control & pressure-control ventilator for invasive and non-invasive ventilation. Trilogy Evo provides noninvasive and invasive ventilator support with added sensitivity for a wide range of adult and pediatric patients. With Care Orchestrator, you have the power to create custom health rules based on your best practices and proven processes. If you treat a patient who has a health issue, including those listed under potential health risks below, or have any problem with a device, report the issue or. It's designed specifically with durability in mind to protect it against damage during travel, such as during medical transport. The Trilogy Evo ventilators with non-conforming foam were distributed to customers in the United States and Korea. UPDATE - On April 7, 2023: The FDA classified Certain Reworked DreamStation CPAP, BiPAP Machines for the Risk They May Deliver Inaccurate or Insufficient Therapy as a Class I recall, the most serious type of recall. Connected Trilogy provides remote viewing of key ventilation parameters, alarm data, device performance and patient usage. This update provides additional information on the recall for people who use repaired and replaced devices. PHILIPS RESPIRONICS RECALL: Click here for more information. Run your business as you see fit, customizing reports and alerts to aid in identifying patients at risk and provide them with timely care. Proven innovations are designed to treat the varying needs of respiratory insufficiency. Volume and pressure modes, AVAPS-AE, SpO2 and EtCO2 monitoring and alarms of every parameter allow for adaptable care. When the PE-PUR foam breaks down, it may: The potential risks of particulate exposure if inhaling or swallowing pieces of PE-PUR foam include: The potential risks of inhaling chemicals released into the device's air tubes from the PE-PUR foam include: During the 2021 manufacturing facility inspection, the FDA obtained additional information, not previously available to the FDA, regarding the silicone-based foam used in a similar device marketed outside the U.S., which failed one safety test for the release of VOCs. The e-learning videos and modules on this Trilogy Evo education curriculum are intended for self- learning and review how to set-up Trilogy Evo for ventilation. In April 2021, Philips first notified the FDA of their intention to conduct a field action due to concerns pertaining to foam breakdown in certain ventilators, BiPAP machines, and CPAP machines. Koninklijke Philips N.V., 2004 - 2023. Trilogy Evo provides noninvasive and invasive ventilator support with added sensitivity for a wide range of adult and pediatric patients. 2022-23 Medinfra India. Add to my planner. Trilogy Evo needs preventive maintenance only every four years, and minimal equipment for calibration. Volume and pressure modes, AVAPS-AE, SpO2 and EtCO2 monitoring and alarms of every parameter allow for adaptable care. Click here for important information about the field safety notice regarding some Philips Respironics Sleep and Respiratory Care devices . Shop for products on our online store of order seamlessly through your own procurement system. Compared to Trilogy 100's All Rights Reserved. Philips makes no representations or warranties of any kind with regard to any third-party websites or the information contained therein. A Philips supplier incorrectly used polyester-based polyurethane (PE-PUR) sound abatement foam, a non-conforming material, in the muffler assembly of the affected Trilogy Evo ventilators. The Trilogy Evo trainings are designed for both Healthcare Professionals and Caregivers or users of the Trilogy Evo. Detachable battery charge time 0% to 80% is 2.5 hours, internal battery charge time 0% to 100% is 3.5 hours. By clicking on the link, you will be leaving the official Royal Philips ("Philips") website. If you have a health issue, including any of the health issues listed above, or any problem with your device, the FDA encourages you to talk to your health care provider and report the problem through the MedWatch Voluntary Reporting Form. Flexibility of circuits allows it to be used in a wide range of patients. CPAP Full Face Masks. Trilogy Evo is a next-generation portable home ventilator that provides invasive and noninvasive positive pressure ventilation for the care of patients weighing 2.5 kg, and it is intended for use by qualified, trained personnel under the direction of a physician. See the latest FDA Actions in the FAQs on Philips Respironics Ventilator, BiPAP Machine, and CPAP Machine Recalls. Identify all of the impacted devices purchased by your organization. Trilogy Evo lets you smoothly transition patients through different care settings using the same clinical technologyfor continuous peace of mind. Transfer data wirelessly to the cloud with safe, secure, connectivity with the Trilogy hub. The PE-PUR foam used in the recalled devices may break down and can result in serious injury, cause permanent impairment, and require medical intervention to prevent permanent injury to users. Introducing Trilogy Evo: Our new, portable life-support ventilator platform designed to: Stay with patients across care settings. Manufacturers, such as Philips, are required to submit medical device reports (MDRs) when they become aware of an event that reasonably suggests that one of their devices may have caused or contributed to a death or serious injury, or has malfunctioned and that device or a similar device marketed by the manufacturer would be likely to cause or contribute to a death or serious injury if the malfunction were to recur. Philips recalled the following devices made between 2009 and April 26, 2021: Philips also recalled certain Trilogy Evo ventilators distributed from April 15, 2021 to May 24, 2021 with specific serial numbers. No duplication of any materials herein is authorized without the express consent of Apria Healthcare Group LLC. Any links to third-party websites that may appear on this site are provided only for your convenience and in no way represent any affiliation or endorsement of the information provided on those linked websites. Emergency Care and Resuscitation Solutions, Radiography | X-ray & Fluoroscopy Solutions, Transition to the future of respiratory care with, For more information on our Philips Learning connection please click here. Handy tips for filling out Trilogy100 Ventilator online. The ventilator can measure, display, record, and alarm oxygen saturation level (SpO2), fraction of inspired oxygen (FiO2), carbon dioxide (CO2) and pulse rate data when integrated with the appropriate accessories. Philips submitted 30 MDRs between 2011-April 2021 that they identified as associated with the PE-PUR foam degradation (breakdown). Philips makes no representations or warranties of any kind with regard to any third-party websites or the information contained therein. Volume and pressure modes, AVAPS-AE, SpO2 and EtCO2 monitoring and alarms of every parameter allow for adaptable care. Any links to third-party websites that may appear on this site are provided only for your convenience and in no way represent any affiliation or endorsement of the information provided on those linked websites. Ventilator-dependent patients are supported by internal and detachable batteries, now with 15-hour battery life. Connected Trilogy Health Rules can be customized with patient-specific ventilator parameters to trigger notifications that proactively identify patients with potential increased need for intervention. Trilogy-100-Ventilator-Information-and-User-Guide. In June 2021, Philips recalled certain ventilators, BiPAP machines, and CPAP machines (see table below) because of potential health risks. Please navigate to the training sections most relevant to you. Break down (degrade) into black pieces that may enter the device's air tubes and be inhaled or swallowed by the user. Your provider may advise you to: Stop using your recalled device (see How to Know if You Should Stop Using Your Device in. Trilogy Evo provides noninvasive and invasive ventilator support with added sensitivity for a wide range of adult and pediatric patients. * Note: Trilogy 100 and 200 ventilators were previously recalled in June 2021 due to the same foam risk. Surgical options, including removing sinus tissue or realigning the jaw. Proven innovations are designed to treat the varying needs of respiratory insufficiency. Any links to third-party websites that may appear on this site are provided only for your convenience and in no way represent any affiliation or endorsement of the information provided on those linked websites. Trilogy Evo provides noninvasive and invasive ventilator support with added sensitivity for a wide range of adult and pediatric patients. Koninklijke Philips N.V., 2004 - 2023. Health care professionals and consumers may report adverse reactions or quality problems they experienced using these devices to MedWatch: The FDA Safety Information and Adverse Event Reporting Program using an online form, regular mail, or FAX. Bacterial filters will not help to reduce exposure to certain chemicals that may be released from the PE-PUR foam. PE-PUR foam is used to lessen sound and vibration in these devices and other medical equipment. An official website of the United States government, Recalls, Market Withdrawals and Safety Alerts, UPDATE: Certain Philips Respironics Ventilators, BiPAP Machines, and CPAP Machines Recalled Due to Potential Health Risks: FDA Safety Communication, Recalled BiPAP or CPAP Machines & Recommendations, Repaired and Replaced BiPAP or CPAP Machines & Recommendations, Potential Health Risks from the PE-PUR Foam, FAQs on Philips Respironics Ventilator, BiPAP Machine, and CPAP Machine Recalls, Certain Reworked Philips Respironics Trilogy 100/200 Ventilators Recalled Due to Potential for Silicone Foam Adhesion Failure and Residual PEPUR Foam Debris, Register your device(s) on Philips' recall website, report the issue or problem through the MedWatch Voluntary Reporting Form, problem through the MedWatch Voluntary Reporting Form, potential risks associated with the use of ozone and ultraviolet (UV) light products for cleaning CPAP machines and accessories, report the problem through the MedWatch Voluntary Reporting Form, FDA's user facility reporting requirements, Philips Respironics Ventilator, BiPAP Machine, and CPAP Machine Recalls, Garbin Plus, Aeris, LifeVent (ventilator). By clicking on the link, you will be leaving the official Royal Philips ("Philips") website. Talk to your health care provider to decide if the plan for your care and treatment should change as a result of this recall. It is important to note the following considerations: Inline bacterial filters will not help to reduce contact with certain chemicals that may be released from the PE-PUR foam. At this time, the information provided by Philips has not established that the filters can reduce the PE-PUR foam's risks. Flexibility of circuits allows it to be used in Any links to third-party websites that may appear on this site are provided only for your convenience and in no way represent any affiliation or endorsement of the information provided on those linked websites. It delivers enhanced performance in noninvasive and invasive ventilation, so patients can be treated with a single device through . Philips EverFlo Oxygen Concentrator 5 Ltr, Philips Respironics Trilogy EVO (OBM) Ventilator, Fresenius Kabi Syringe and Infusion Pumps, Check Out Philips Everflo Oxygen Concentrator, 35 2000 ml on Dual Limb and Active Flow circuits, 50 2000 ml on passive and active PAP circuits, 0 35 cmH20 for active circuits 3 25 cmH20 for passive circuits, Off, AutoTrak, Sensitive, AutoTrak, and Flow Trigger, Synchronized intermittent mandatory ventilation (volume control), Mouthpiece ventilation (pressure control), Synchronized intermittent mandatory ventilation (pressure control), 15 hours nominal total run time per method in IEC 80601-2-72 (7.5 hours each battery), from 0% to 80%: 2.5 hours; from 0% to 100%: 3.5 hours, 16.5 cm D x 28.6 cm W x 24.5 cm H 6.48 D x 11.25 W x 9.65 H. Review the recommendations above with patients who use the recalled devices, including that for some patients, stopping use of the device may involve greater risk than continuing to use the recalled device. Philips makes no representations or warranties of any kind with regard to any third-party websites or the information contained therein. six-hour battery, Trilogy Evo gives patients a new level of freedom and mobility. Through its 15-hour battery life, it provides you the next level of mobility so you can achieve a higher quality of life during treatment. Nominal run time per method in InternationalElectrotechnicalCommission (7.5 hr/battery). Intended to inform you of the innovative Trilogy family trilogy ventilator evo in these devices and other medical equipment Philips. This is a 10-pack of particulate filters for use in its respective.. ; on & quot ; on & quot ; on & quot ; on & quot ; 3 #. Pe-Pur foam, from newborns to adults or the information contained therein on-screen. Trigger notifications that proactively identify patients with potential increased need for intervention, now with battery! Device these parts were installed into is not a Part of this.... 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