remede.zoll.comCentral Sleep Apnea (CSA) Treatment | remedē®

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Description:remedē®, an implantable therapy that activates automatically to treat the harmful effects of central sleep...

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System Search the remedē® System website About Careers Newsroom Blog Contact Clinicians Home Central Sleep Apnea rem edē System Patient Stories Getting rem edē About Careers Newsroom Blog Contact Clinicians Central Sleep Apnea rem edē System Patient Stories Getting rem edē About Patient Stories Find a Doctor Important Safety Information About Patient Stories Find a Doctor Important Safety Information Search the remedē® System website Treat central sleep apnea without masks or medications Living with central sleep apnea (CSA) can be exhausting. But with the rem edē ® System, you can finally get the sleep you need to take back your days. Are you looking for relief from CSA? If you’re like many people living with central sleep apnea, you haven’t found a treatment that works–or lasts. That’s why we developed the rem edē System, the first FDA-approved non-mask therapy designed to treat moderate to severe CSA in adults. rem edē is an implantable device that activates automatically and restores a more normal breathing pattern, so you can sleep peacefully—and have more energy for what you love. Learn more about CSA and rem edē Understand CSA Central sleep apnea is a serious disorder that causes disrupted breathing during sleep. Know the symptoms, causes, and how to find out if you have CSA. Learn About CSA Discover rem edē Learn about an FDA approved non-mask treatment for CSA. LEARN ABOUT rem edē Getting rem edē Understand the process of getting rem edē and find a doctor near you who can help determine if you are a candidate. INTERESTED in rem edē ? Real people, real impact Hear from rem edē patients who share their experiences living with CSA, how they got the rem edē System, and how it’s improved their lives. WATCH PATIENT STORIES Am I a candidate for rem edē ® ? Important Safety Information The rem edē ® System is indicated for moderate to severe Central Sleep Apnea in adult patients. Your doctor will need to evaluate your condition to determine if the rem edē System is right for you. The rem edē System is MR Conditional but conditions apply. Please make sure that your physician knows about the conditions and precautions to ensure safety, which can be found in the rem edē System MRI guidelines manual. You should not have the rem edē System implanted if you have an infection and you will not be able to have diathermy (special heat therapies) after implantation. The rem edē System may be used if you have another stimulation device such as a heart pacemaker or defibrillator; special testing will be needed to ensure the devices are not interacting. As with any surgically implanted device, there are risks related to the surgical procedure itself which may include, but are not limited to, pain, swelling, and infection. Once the therapy is turned on, some patients may experience discomfort from stimulation and/or from the presence of the device. The majority of these events are resolved either on their own or by adjusting the therapy settings. The rem edē System may not work for everyone. There are additional risks associated with removing your system. If you and your doctor decide to remove the system, another surgery will be required. Be sure to talk with your doctor so that you thoroughly understand all of the risks and benefits associated with the implantation of the rem edē System. Rx only. For further information, please visit remede.zoll.com, call +1-952-540-4470 or email info@remede.zoll.com . 12400 Whitewater Dr., Suite 150 Minnetonka, MN 55343 USA 952-540-4470 info@remede.zoll.com Important Safety Information About Contact Indication for use: The rem edē ® System is an implantable phrenic nerve stimulator indicated for the treatment of moderate to severe central sleep apnea (CSA) in adult patients. Read full indications for use The rem edē ® System, rem edē ® EL System, and rem edē ® EL-X System have received FDA approval. The rem edē ® System model 1001 has received CE Mark approval. Copyright © 2023 ZOLL Medical Corporation. All rights reserved. Respicardia and rem edē are registered trademarks of ZOLL Respicardia, Inc. in the United States and/or other countries. ZOLL is a registered trademark of ZOLL Medical Corporation in the United States and/or other countries. © 2024 ZOLL Medical Corporation. Patents Privacy Policy Terms of Use Am I a candidate for rem edē? Contact Us Manage Cookie Consent To provide the best experiences, we use technologies like cookies to store and/or access device information. Consenting to these technologies will allow us to process data such as browsing behavior or unique IDs on this site. Not consenting or withdrawing consent, may adversely affect certain features and functions. Functional Functional Always active The technical storage or access is strictly necessary for the legitimate purpose of enabling the use of a specific service explicitly requested by the subscriber or user, or for the sole purpose of carrying out the transmission of a communication over an electronic communications network. Preferences Preferences The technical storage or access is necessary for the legitimate purpose of storing preferences that are not requested by the subscriber or user. Statistics Statistics The technical storage or access that is used exclusively for statistical purposes. 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