Downloadable materials and support to help you learn more about the StimRouter PNS System.
StimRouter PNS User Guide
This guide contains helpful information on the user kit components, operating instructions, and maintenance requirements for the StimRouter Neuromodulation System.
DownloadStimRouter PNS E-EFC User Guide
This guide contains helpful information on the user kit components, operating instructions and maintenance requirements for the StimRouter Neuromodulation System.
DownloadStimRouter PNS Clinician Guide
This guide contains helpful information on the user kit components, operating instructions and maintenance requirements for the StimRouter Neuromodulation System.
DownloadBattery Life Guidelines for StimRouter PNS
Guidelines for maximizing the battery life of your StimRouter PNS system.
DownloadStimRouter PNS Product Brochure
Information about the StimRouter PNS system as a treatment for chronic pain.
DownloadElectrode Selection Guide for StimRouter PNS
Guidelines for helping to choose the best electrode size for your StimRouter implant.
DownloadStimRouter PNS User Reference Card
This card is a quick reference, including StimRouter PNS setup, patient programmer operating instructions, electrode and EPT removal, and troubleshooting.
DownloadPatient Information and Medical Release Form (Form 1) – US
Patient Information and Medical Release Form for StimRouter PNS. This form is intended for United States users.
DownloadWarranty Card for the StimRouter PNS
This card contains helpful details of the StimRouter PNS Neuromodulation System’s one-year limited warranty.
DownloadMedical Device ID Card for StimRouter PNS
StimRouter Medical Device Identification Card for patients who need a replacement Medical Device ID Card.
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Rx Only. The StimRouter Neuromodulation System is indicated for pain management in adults who have severe intractable chronic pain of peripheral nerve origin, as an adjunct to other modes of therapy (e.g. medications). The StimRouter is not intended to treat pain in the craniofacial region. StimRouter is contraindicated in patients who have any active implanted device such as an implanted demand cardiac pacemaker or defibrillator, or metallic implant in the immediate area intended for implant. For complete instructions for use, storage, warnings, indications, contraindications, precautions, adverse reactions and disclaimer of warranties, please refer to the insert accompanying each product or online at www.stimrouter.com.