The ZEPU-AI1 is a gait-training neuro-rehabilitation robot designed to assist stroke patients and others with mobility challenges to regain walking ability. It supports both upper- and lower-limb training and is intended for use in clinics, rehab centers, hospitals, and home settings.
Key features include combined upper- and lower-limb training capability, service-free spare parts for reduced maintenance, CE and ISO certification for quality and safety, and a compact design suitable for varied clinical and home environments.
The device is classified as a Class I instrument and is CE and ISO certified.
The device dimensions are 2750 x 1100 x 2350 mm. Additional clearance may be required for patient access and therapist movement—please consult the manufacturer for recommended installation footprint and room layout.
The robot is intended for stroke patients and others with gait impairments. It is used for rehabilitation to improve walking skills and mobility, and for physical therapy in clinical and home-based programs.
The robot is suitable for clinics, rehab centers, hospitals, and home use. For home installation, ensure appropriate space, supervision plans, and that a clinician has approved the device for the patient’s home program.
Yes. Rehabilitation robots should be used under the guidance of trained clinicians or therapists, particularly during initial sessions or for patients with significant deficits, to ensure safety and proper therapy progression.
The product is designed with service-free spare parts to minimize routine maintenance. Routine checks, cleaning, and following the manufacturer's maintenance guide are still recommended. For detailed maintenance schedules and procedures, contact the supplier.
The MOQ is 1 piece. The supplier's stated supply ability is 20 sets per month. To place an order or confirm availability, contact the manufacturer or authorized distributor.
Yes. OEM options are available. Contact the manufacturer to discuss customization, branding, software or hardware options, and lead times for customized units.
Units are packaged in wooden boxes for dispatch. The stated port of dispatch is Qingdao. For shipping quotes, export documentation, or special packaging requests, contact the supplier.
Warranty terms and technical support options are not specified in the product listing. Please contact the manufacturer or distributor for detailed warranty coverage, service contracts, training, and local support availability.
Specific contraindications are not listed in the product information. As with all rehabilitation equipment, use should be cleared by a treating physician and implemented by trained personnel. Patients with unstable medical conditions, severe osteoporosis, uncontrolled seizures, or other contraindicating conditions should not use the device until cleared by a clinician.
Software features and data-tracking capabilities are not detailed in the provided description. For information about therapy programs, data export, user interfaces, and electronic records, please request the product datasheet or software specification from the supplier.
For full technical specifications such as electrical requirements, patient weight and size limits, installation instructions, and detailed clinical guidelines, contact the manufacturer or authorized distributor directly. They can provide the complete technical file and user manual.
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