Is the H200 Wireless right for me?
The H200 Wireless helps people who have disorders of the central nervous system that result in functional deficits and impairments of the arms and hands, including:
- Stroke
- Traumatic brain injury
- Spinal cord injury
- Certain neurological disorders
Getting Started
If the H200 Wireless may be right for you, here are next steps:
1.
Preliminary Screening
Contact us to complete a preliminary screening. We’re available by:
- Phone at 855-902-5252
- Email at [email protected]
2.
Evaluation
We can help you schedule a free evaluation with a qualified clinician who can determine whether the device is appropriate for you.
If so, we can help you obtain a Prescription and Medical Release Form from your healthcare provider.
For help starting a conversation with you doctor, read our Doctor Discussion Guide.
3.
Acquisition
After we receive your prescription and Medical Release Form, we will verify your insurance coverage, submit authorization documents, and talk with you about your options for getting the H200 Wireless to you.
Success Stories
See how the H200 Wireless Hand Rehabilitation System has changed patients’ lives.
Contact us to schedule a demo with H200 Wireless or if you have questions about other Bioness products.
Indications for Use:
The H200 Wireless System is an electrical stimulation device indicated for the following uses:
- Functional Electrical Stimulation (FES)
- Improvement of hand function and active range of motion in patients with hemiplegia due to stroke or upper limb paralysis due to C5 spinal cord injury.
- NeuroMuscular Electrical Stimulation (NMES)
- Maintenance and/or increase of hand range of motion; Prevention and/or retardation of disuse atrophy; Increase in local blood circulation; Reduction of muscle spasm; Re-education of muscles.
H200 Wireless is contraindicated in patients with a demand-type cardiac pacemaker, defibrillator or any electrical implant. Do not use the system on a hand where metallic implant is directly underneath the electrodes, a cancerous lesion is present or suspected, or on a hand with regional disorder (e.g., fracture or dislocation) which could be adversely affected by motion from the stimulation. Use caution in patients with diagnosed or suspected cardiac problems or epilepsy.
Full prescribing information can be found in product labeling or at www.bionessrehab.com/h200/safety-information/.
Instructions for Use / Patient Guides and Reference Cards can be made available upon request.
Contact [email protected] or 800-211-9136 to request an electronic copy.