THE LATEST ADVANCEMENT IN

remedē® SYSTEM TECHNOLOGY

THE LATEST ADVANCEMENT IN

remedē® SYSTEM TECHNOLOGY

remede_EL-X_system

The remedē EL-X System is a next generation platform combining enhanced functionality with a patient-friendly design that simplifies the implant procedure and delivers long-lasting benefits to your adult patients with central sleep apnea.

NEXT GENERATION PLATFORM

Extended longevity

Long-lasting battery life extended by 40% from previous platform1

Patient-friendly design

Small and thin; size decreased by 25% from previous model1 with rounded edges designed for comfort

Remede EL-X

SIMPLIFIED IMPLANT

Single lead, single port system

Delivers stimulation and senses respiration from a single lead, simplifying the implant experience

NEXT GENERATION remedē REPORTS

Enhanced with DRēAM View

remedē Reports software is designed to deliver insightful information for you to efficiently tailor therapy for your patients. The latest enhancement, DRēAM View, provides an enhanced set of full-night, comprehensive, and detailed diagnostic data.

Remede-EL-X

remedē EL SYSTEM

Built on the same next-generation platform, the remedē EL is designed for compatibility with current IS-1 leads.

1. FDA PMA P160039, Supplement 006, Physician Manual.
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For Patients

IMPORTANT SAFETY INFORMATION

The remedē® 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 remedē system is right for you. You will not be able to have an MRI or diathermy (special heat therapies) if you have the remedē system implanted. The remedē 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 remedē 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 remedē system. Rx only. For further information, please call +1-952-540-4470 or email info@respicardia.com.