The Strokes Stimulator TDCS (Model E-TDCS02 by ELITEMED) is a transcranial direct current stimulation device designed to support post-stroke neurorehabilitation by delivering low‑intensity electrical stimulation to promote recovery as part of a rehabilitation program.
This device should be used under the guidance of a qualified healthcare professional. Use at home is possible only with professional instruction and an established treatment plan.
It is intended for post-stroke neurorehabilitation and for supporting brain-function enhancement through transcranial electrical stimulation in hospitals, rehabilitation centers, and supervised home settings.
The Strokes Stimulator TDCS is electric and uses a plug-in power supply mode. It does not contain an internal battery.
The product is ISO13485 certified and is classified as a Class II instrument, indicating it is subject to regulatory controls for safety and performance.
Contraindications and precautions should be reviewed with a clinician. Generally, transcranial electrical stimulation is approached with caution in people with implanted electronic medical devices (e.g., pacemakers), seizure disorders, open cranial wounds, or pregnancy. Always consult a healthcare professional before use.
Yes. Online technical support is available. Contact details and support procedures are provided in the product manual or via the ELITEMED support channels.
The housing is made of durable ABS material. Clean the exterior with a soft cloth dampened with mild detergent; do not immerse the device in liquid or use abrasive cleaners. Follow the user manual for electrode and accessory cleaning instructions.
Use electrodes and accessories recommended by ELITEMED or those specified in the user manual. If using third‑party electrodes, confirm compatibility and safe connection with the manufacturer or clinician before use.
Yes. Proper training in tDCS application, electrode placement, device settings, and monitoring is recommended for clinicians and caregivers to ensure safe and effective use.
The listed shelf life is 1 year. Single package dimensions are 46 x 51 x 37 cm and the single gross weight is approximately 9.000 kg.
No. The device is intended to support neurorehabilitation as an adjunct to conventional therapies (physical, occupational, speech therapy). Treatment plans should be determined by rehabilitation professionals.
Perform routine visual inspection of the unit, power cord, connectors and electrodes before each use. Follow the maintenance schedule in the user manual. Seek professional servicing for any faults; do not attempt to repair internal components yourself.
Stop using the device immediately, disconnect it from power, and contact ELITEMED technical support or your supplier. Report any adverse events to your clinician and follow local medical device adverse event reporting procedures.
For detailed clinical data, regulatory status in your country, or instructions for use, refer to the product manual and ELITEMED’s official documentation or contact their customer support.
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