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    ALFESS

    Brand: Allard
    TGA Approved: 327782

    ALFESS™ is a Functional Electrical Stimulation (FES) device intended to improve gait when foot drop or diminished foot and toe clearance is present. It assists the nerves of tibialis anterior to actively dorsiflex the foot.

     

    SKU: WEB000932
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    Code Size Unit of Measure
    Code: 282700612 Size: Universal Unit of Measure: EA

    ALFESS™ is a new modern device, intended to improve gait when foot drop, diminished foot and toe clearance is present. It assists the nerves of tibialis anterior to actively dorsiflex the foot. The device is applied to the upper part of the lower leg. During walking, sensors identify speed and angles of the leg to adapt to the walking pattern. An algorithm processes the information and sends out electrical impulses to the nerves to lift the forefoot. The user can easily increase or decrease the level of stimulation at any time.

    The unit has a sleek and conforming shape, works well for bilateral use. Thanks to magnetic clasp and unique controls the unit can be operated with one hand!
    The training mode assists to achieve the best rehabilitation result. Training can be done either with the patients clinician, or the patient can do training independently after being provided with clear instructions.

    The unit is easy to handle and charge. Control settings on the device, or with remote control provided, or via Smart Phone App.

    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.

     

    Product Files
    Document Title Description
    ALFESS IFU Download
    ALFESS Graphic Instructions Download
    ALFESS Brochure Download
    ALFESS Programming / Evaluation Schedule Download
    ALFESS Programming Refresher Download
    View ALFESS OPEDucate Course Download

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