philips respironics dreamstation registration philips respironics dreamstation registration

Heres How to Get Low-Cost or Free CPAP Supplies! The DreamStation 2 CPAP Advanced is designed to provide a simplified user experience, including a premium color touchscreen with fewer panes to navigate. If you are using a mobile device to transfer your data, we recommend using a second device to read through the step-by-step instructions for an easier set up and transfer process. You can sign up here. Dont have one? Then you can register your product. Proof of purchase may be required to take advantage of a promotion or request a repair within warranty. Learn About Sleep Apnea and Treatment Options, The Latest CPAP Machine Reviews from Experts, Find the Best CPAP Mask for Your Lifestyle, Our Top Picks to Make CPAP Cleaning a Breeze, Were here to help! Enter your Username and affected Device Serial number. The foam that is used in some devices to reduce sound and vibration showed signs of degradation (damage) and chemical emissions. Are there any recall updates regarding patient safety? Questions about next steps after you have transferred your prescription settings? You will be using Bluetooth to transfer your therapy results to the DreamMapper app. You are about to visit the Philips USA website. While recalled devices contained a polyester-based polyurethane (PE-PUR) sound abatement foam component, the sound abatement foam in all new and remediated devices is a silicone foam*. This is a potential risk to health. Please visit mydreammapper.com by clicking the Login button above. To register a new purchase, please have the product at hand and log into your MyPhilips account. You are about to visit a Philips global content page. 1. Receiving party (contact information):Affiliates other than KoninklijkePhilips N.V.(contact information of responsible division:privacy@philips.com) Cant Afford a New CPAP Machine? Please be assured that we are treating this matter extremely seriously, and are working to address this issue as efficiently and thoroughly as possible. We have completed all requests by Philips Respironics and we eagerly await a plan that will allow us to provide actionable solutions to customers. Approve a rental device of the same caliber and quality as your original equipment, Determine that the recall voids the standard replacement requirement and immediately replace the device, Deny covering the cost of a new machine at this time. Once set, the device will automatically start at the selected Ramp Plus pressure with all future therapy sessions. This new assessment is limited to the evaluation of VOCs for first-generation DreamStation devices and does not evaluate the risks of potential foam particulates or cover other devices affected by the recall. To register your product, youll need to log in to your My Philips account. Success. Questions about registering, signing in or need any otherDreamMapper support? We strongly recommend that customers and patients do not use ozone-related cleaning products. Koninklijke Philips N.V., 2004 - 2023. If you continue using your device, please note that ozone is referenced by Philips Respironics as a potential contributing factor to degraded foam. The recall is for all Philips Respironics CPAP/BiPAP units (excluding the new Dreamstation 2 unit). The FDA is still considering the data and analyses that Philips Respironics has provided and may reach different conclusions. Auto CPAP Advanced. Healthcare providers, patients, and other stakeholders should use the complete update, including information on the limitations of the testing, for any informed decision making and should not solely rely on the overview presented here. Register - Philips Respironics DreamMapper Register Country* First Name Last Name Email Address* Confirm Email Address* Mobile Phone Primary Device Serial Number I understand and accept the Terms and Conditions. Register the device on the recall website www.philips.com/src-updates The website provides current information on the status of the recall and how to receive permanent corrective action to. If you do not have a second device available we suggest you print out the instructions. The risks include that the foam may degrade under certain circumstances, influenced by factors including use of unapproved cleaning methods, such as ozone.Product DescriptionThe Philips Respironics . When we refurbish the affected devices with a new blower and air pathway, we also clean and disinfect them. We are absolutely committed to supporting the worldwide community of patients who rely on our Sleep & Respiratory Care solutions for their health and quality of life, and the physicians and customers who are dedicated to meeting patient needs., Philips Respironics identified there is risk the PE-SUR sound abatement foam may degrade into particles which may enter the devices air pathway and be ingested or inhaled by the user, and the foam may off-gas certain chemicals. DreamMapper is part of the Dream Family from Philips Respironics. Philips Respironics Chief Executive Frans van Houten said, Were going to put all our capacity to focus entirely on replacing and repairing these units, a process he said would likely take a year. Additionally, Philips Respironics suggests patients review the age of their devices, as they are typically recommended to be replaced after five years of use. As new information and options become available to help our customers we will switch our operations accordingly. The issue is with the foam in the device that is used to reduce sound and vibration. You can also upload your proof of purchase, so it is stored safely if you need it for service or repair of your product. Register your product and start enjoying benefits right away. Our site can best be viewed with the latest version of Microsoft Edge, Google Chrome or Firefox. To register your product, youll need to. You can sign up here. What is the safety issue with the device? You can refuse to provide the Authorization for Collection and Use of Sensitive Information. As a result, testing and assessments have been carried out. You can log in or create one. Items of Personal Information to be Collected If your product is eligible for extended warranty, first you need aMyPhilipsaccount. Review of this assessment has determined that exposure to the level of VOCs identified to date for the first-generation DreamStation devices is not typically anticipated to result in long-term health consequences for patients. Please be assured that our teams are working on a comprehensive remediation program to support patients with an affected device. Products that are not affected may have different sound abatement foam material, as new materials and technologies have become available over time. High heat and high humidity environments as well as unapproved cleaning methods such as ozone, may also contribute to foam degradation. We have trained service professionals on hand who can make sure that the affected foam is completely removed, safely, and that the new silicone foam is inserted correctly. 2. We understand that the situation may cause you some anxiety and you may feel uncertain about what to do next. Click Return to Login after successful password reset. You can refuse to provide the Authorization for Collection and Use of Personal Information. Our update in November 2021 provides broadened guidance regarding affected CPAP, BiLevel PAP and Mechanical Ventilator devices, and mechanical ventilators, as follows: For patients using BiLevel PAP and CPAP devices, talk to a health care provider to decide on a suitable treatment for medical conditions, which may include: Using another similar device that is not part of the recall. Click Next. At the Login Page for DreamMapper, you can register for a new account or login with your existing Username and Password. What is the advice for patients and customers? We know that you are eager to find out when youll receive your replacement CPAP, BiPAP or Mechanical Ventilator device. Your patients may receive a DreamStation 2 as a replacement for their affected CPAP device. Flurry Analytics uses cookies or similar techniques, which are text files placed in your App, in order to help the App to analyze overall traffic patterns through our App. Select country / language; Breathe easier, sleep more naturally . Per Philips Respironics, possible health risks include exposure to degraded sound abatement foam and exposure to chemical emissions from the foam material. We have trained service professionals on hand who can make sure that the affected foam is completely removed, safely, and that the new silicone foam is inserted correctly. Have your DreamStation device serial number available (begins with the letter J and is 13 characters in length). When you provide the Authorization for Collection and Use of Personal Information below, you can use services for improved enhance treatment adherence through this application. If you are considering purchasing a new machine to replace your Philips Respironics device, you must have a current prescription. By transmitting the information generated by the cookie about the use of the App to Flurry, your setting ensures that IP address is anonymized before geo-localization and will be replaced by a generic IP address before storage. You can log in or create one. Dont have one? Please review the DreamStation 2 Setup and Use video for help on getting started. When we refurbish the affected devices with a new blower and air pathway, we also clean and disinfect them. Begin SD data card transfer Once you have successfully logged in, please open the instructions below for specific instructions on how to transfer the data from your current device to DreamMapper. DreamStation Go: Whether you're traveling for business or venturing out on the vacation of a lifetime, DreamStation Go provides an easy, reliable and portable PAP experience for users who . Our update in November 2021 provides broadened guidance regarding affected CPAP, BiLevel PAP and Mechanical Ventilator devices, and mechanical ventilators, as follows: For patients using BiLevel PAP and CPAP devices, talk to a health care provider to decide on a suitable treatment for medical conditions, which may include: Stopping use of an affected device Using another similar device that is not part of the recall Continuing to use an affected device, if a patients health care provider determines that the benefits outweigh the risks identified in the recall notification. Proof of purchase may be required to take advantage of a promotion or request a repair under your warranty. If you do not have a second device available we suggest you print out the instructions. Items of Sensitive Information to be Collected By clicking on the link, you will be leaving the official Royal Philips Healthcare ("Philips") website. When we refurbish the affected devices with a new blower and air pathway, we also clean and disinfect them. You should have received a letter from Philips about this issue that contains log-in credentials for the registration website. Amsterdam, the Netherlands - Royal Philips (NYSE: PHG; AEX: PHIA) today provides an update on the comprehensive test and research program of its subsidiary Philips Respironics, following the voluntary recall notification/field safety notice* to address potential health risks related to the polyester-based polyurethane (PE-PUR) sound abatement foam in specific CPAP, BiPAP and mechanical . You can register your device at https://www.philipssrcupdate.expertinquiry.com or call their registration line at 877-907-7508. Intuitive. Products not affected by this recall notification (U.S. only) / field safety notice (International Markets) include: The best way to know if your device is included in the recall is to register your machine for the recall. 2. Once you have successfully logged in, please open the instructions below for specific instructions on how to transfer the data from your current device to DreamMapper. Register your device (s) on Philips Respironics' recall website to stay informed of updates from Philips Respironics regarding any new instructions or other corrective fixes, which the. Fill out the registration form (leave Mobile Phone blank). Registration Link: https://www.usa.philips.com/healthcare/e/sleep/communications/src-updateWe wanted to share our step-by-step walkthrough of the process to register your CPAP machine / BIPAP machine/mechanical ventilator devices for the Philips Respironics Recall. Create a new password following the password guidelines. If you already have a DreamMapper account but do not remember your Username, please note that your Username is your email address. If you are a patient who has been affected by this recall, please do not try to remove the foam from your device. (This includes a request for temporary suspension of the 90-day adherence rule for continued coverage of a PAP device.). You can also upload your proof of purchase should you need it for any future service or repairs needs. Philips Respironics guidance for healthcare providers and patients remains unchanged. As a reminder, we recommend using a second device to read through the step-by-step instructions for an easier set up and transfer process. Please review the attached. 3. Select your mask type and specific mask model. All oxygen concentrators, respiratory drug delivery products, airway clearance products. Due to technical reasons, we are currently not supporting registrations for medical devices like CPAP and BIPAP. Enter your Username and affected Device Serial number. The CPAP team strives to provide insightful and meaningful information to its audience, keeping you in the know on the latest happenings in the sleep health and respiratory world. Also, sound abatement foam in unaffected devices may be placed in a different location due to device design. Proof of purchase is a printed receipt from the shopwhere you purchased your product, or a PDF invoice from an online retailer. After careful analysis, we issued a Recall Notification in the US and a Field Safety Notice in other markets. Using alternative treatments for sleep apnea. Please be assured that we are doing all we can to resolve the issue as quickly as possible. In compliance with Philips instructions and standard recall practices, CPAP.com is not replacing recalled products with current stock nor issuing refunds for past orders. If you do not remember your DreamMapper password or need to reset it: Bluetooth pairing and data transfer Once you have successfully logged in, please select your mobile device operating system below for specific instructions on how to transfer the data from your current device to DreamMapper. If you do not have a second device available we suggest you print out the instructions. No matter what type of health insurance coverage you have, you should call your health insurance group soon to see which steps you need to take once youve registered your device and spoken with your doctor. Philips Sleep and Respiratory Care Devices - Australia and New Zealand Register your device On April 26, 2021, Philips globally provided an important update to the market regarding proactive efforts to address identified issues with a component in certain products of our Sleep & Respiratory Care portfolio. First Night Guide. Consultation with health care providers about using an inline bacterial filter with ventilators, which may help to filter out particles of foam, as indicated in the Philips recall notification, which also notes limitations of this option and areas of caution. Learn more about the full recall process here. 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