User's Manual

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Humidity limitation
Atmospheric pressure limitation
Contraindications
 Do not use the device where a cancerous lesion in present or suspected.
 Do not use the device if you have a cardiac pacemaker, implanted defibrillator, or other implanted metallic or
electronic device. Use of the device in conjunction with any of the above may cause electric shock, burns, electrical
interference, or death.

Do not use the device on an arm where a regional disorder, such as a fracture or dislocation, would be adversely
affected by motion from the stimulation.
Warning

Do not use the XFT-2003EA while receiving any MRI scan.

Do not use the XFT-2003EA while sleeping, bathing or operating a vehicle.

The long-term effects of chronic electrical stimulation are unknown.

Stimulation should not be applied over the carotid sinus nerves, particularly in patients with a known sensitivity to the
carotid sinus reflex.
 Stimulation should not be applied over the neck or mouth. Severe spasm of the laryngeal and pharyngeal muscles may
occur and the contractions may be strong enough to close the airway or cause difficulty in breathing.
 Stimulation should not be applied transthoracically in that the introduction of electrical current into the heart may
cause cardiac arrhythmias.
 Stimulation should not be applied over swollen, infected, or inflamed areas or skin eruptions, e.g., phlebitis,
thrombophlebitis, varicose veins, etc.
 Stimulation should not be applied over, or in proximity to, cancerous lesions.

The safety of usage during pregnancy has not been determined.

Electrode positioning and stimulation parameters’ setting should be conducted by professionals. If you keep feeling
uncomfortable stimulation or experience a skin irritation or rash please stop using this product.

Please do not position the electrode in the area of malignant neoplasms, neck arteries (throat) or thrombus.

Please do not position the electrode on the affected skin or other affected area, such as fracture and dislocation.
 Please use with caution when the arteries of used area show partial occlusion, when the patient has vascular atrophy
because of hemodialysis, or when the vascular system shows instability.
 Please use with caution if the used areas have structural deformity.
 This product should be prescribed by a physician.
 Please stop using this product if the body shows any unforeseen adverse medical condition while using this device.
FCC warning
Any Changes or modifications not expressly approved by the party responsible for compliance could void the user's authority to