ALFESS

Recommended Range Of Application:

Central Nervous System diagnosis such as:

• Multiple Sclerosis (MS)
• Stroke (CVA) 
• Cerebral Palsy (CP)
• Incomplete Spinal Cord Injury
• Traumatic Brain Injury (TBI).

Contraindications:

• Do not use with electronic monitoring equipment, NMR-imaging, defibrillator or high-frequency medical device.
• Not to be used on patients with cardiac demand pacemakers.
• Do not use near metal implants (knee/ankle replacement or pins and plates)
• Do not use over broken skin or sunburn.
• Do not use near malignant tumours.
• Do not use if you have a history of autonomic dysreflexia.
• Do not use FES following recent surgery where muscle contraction may disrupt the healing process.
• Seek medical advice regarding use if pregnant.

For more information about precautions and warnings please read Instructions for use.

Disclaimer: ALFESS is a class 2 FES device and must be custom programmed to a patient to suit their gait pattern and stimulation requirements. Orthotists, Physiotherapists and some podiatrists are qualified to fit and program the device. If you require a recommendation to a trained clinician in your area or if you are one of the above allied health professionals and would like training yourself, please get in touch with OPC.

OPC can not guarantee FES products that have not been programmed by a trained allied health professional.

All units contain serial numbers for tracking and warranty purposes.