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Sep 27, 2023 · Globally, we have remediated 99% of actionable* sleep therapy device registrations to date. As the remediation of the ventilator devices continues, Philips Respironics will be communicating with Durable Medical Equipment providers (DMEs) directly throughout the process.
- Information for Patients
Following ongoing communications, Philips Respironics agreed...
- News & Updates
An update on our progress . Globally, we have remediated 99%...
- Ozone Cleaner Information
Begin registration process. 877-907-7508. If you haven't yet...
- Contact and Support
Please call our registration line or visit our registration...
- Information for Clinicians
Together with five independent, certified testing...
- Understanding The Recall Process
Your device registration is matched to your DME; A device...
- Information for Patients
Product registration. To register a new purchase, please have the product on hand and log into your My Philips account. Click here to register a device affected by the recall of certain Philips Respironics Sleep and Respiratory Care devices.
People also ask
What happens after I Register my Philips device?
How many actionable* sleep therapy device registrations have been remediated?
How will Philips Respironics communicate with DMEs during the remediation process?
Register affected devices on the recall notification (U.S. only) / field safety notice (International Markets) website, www.philips.com/SRC-update.
Download the app Using your mobile device: Download the DreamMapper app by using the app store buttons above. Create New Account Fill out the registration form. Have your DreamStation device serial number available (begins with the letter “J” and is 13 characters in length).
Jun 29, 2023 · Please log-in to the Patient Portal for device specific instructions on how Philips Respironics can obtain your prescription and fulfill your replacement device. Depending on your specific situation, you may be eligible to select an Auto-adjusting CPAP replacement device.
Sep 27, 2023 · Register your device (s) Questions and answers. Support line 0800 249 4578 (UK) or (0044) 20 8089 3822 (outside of UK) Questions and answers.
If you have not done so already, please click here to begin the device registration process. Our update in November 2021 provides broadened guidance regarding affected CPAP, BiLevel PAP and Mechanical Ventilator devices, and mechanical ventilators, as follows: