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The Cervical Neck and Lumbar Traction Device Traction Table (JYZ-IIB) is a state-of-the-art physiotherapy device designed for spinal traction therapy. This versatile equipment helps to relieve back and neck pain through adjustable traction settings, making it ideal for use in rehabilitation centers and clinics.
The Cervical Neck and Lumbar Traction Device (JYZ-IIB) is an essential rehabilitation tool designed to relieve pain and improve mobility for patients with cervical or lumbar spinal issues, offering a safe and effective therapy solution.





Advantages
1.Integrated cervical and lumbar traction can be performed for different patients respectively, saving the use of space and
reducing costs.
2.Computer control cervical traction, patients have emergency switch, time and force are controlled by the program, fully realize automation.
3.20 kinds of treatment plan memory reading, more convenient for clinical operation.
Scope of application
Suitable for cervical and lumbar traction.
Contraindications
1. Severe heart, brain and lung diseases or extreme weakness.
2. Patients with bleeding tendency and blood diseases.
3. Patients with severe local skin damage and skin diseases.
4. Patients with infectious diseases, osteoarthritis tuberculosis,osteomyelitis, bone tumors, severe osteoporosis, spinal injury or with spinal cord symptoms.
5, pregnant women more than three months, excessive hunger and drunk state, serious hypertension patients, etc.
6, patients with mild hypertension should not use for too long each time.
Product parameter
No approved technical specifications are available yet. Please refer to the product description or contact our team.
The JYZ-IIB is a physiotherapy traction table designed to provide controlled cervical and lumbar spinal traction to help relieve neck and lower back pain, improve mobility, and support rehabilitation in clinics and rehabilitation centers.
The device provides adjustable cervical traction up to approximately 300 N and lumbar traction up to approximately 990 N, allowing clinicians to select the appropriate force for each patient.
Traction time is adjustable from 0 up to 9 minutes per session via the device's control system.
The device operates on AC 220 V, 50 Hz power. It is designed for plug-in operation—ensure your clinic's electrical supply matches these requirements.
Safety features include computer-controlled time and force limits, an emergency stop switch accessible to the patient, and program-controlled traction sequences. The unit is CE certified and meets MOL safety standards.
Contraindications include patients with severe heart, brain or lung disease, bleeding disorders, severe skin disease or local skin damage, active infections (e.g., osteomyelitis, tuberculosis), bone tumors, severe osteoporosis, acute spinal injuries or cord compression, pregnancy beyond three months, uncontrolled hypertension, severe weakness, intoxication, or other conditions specified by a clinician.
Yes. Traction should be administered by trained clinical staff or under the supervision of a qualified physiotherapist or physician who can assess indications, set appropriate force/time, and monitor patient response.
Force and time are adjusted from the device's computer control panel. The unit allows you to set traction force levels and program durations, and it stores up to 20 treatment plans for easy recall.
Unplug the device before cleaning. Wipe surfaces with a mild disinfectant and soft cloth—do not immerse the unit or spray liquids directly into controls. Regularly inspect power cords, straps, fasteners, and mechanical components for wear. Arrange authorized technical service for calibration and repairs.
Check that the unit is plugged into a working outlet with correct voltage, ensure the main switch and emergency switch are not activated, inspect fuses or circuit breakers, and verify connectors. If the problem persists, contact the supplier or authorized service technician.
The traction table is compact, with dimensions of 1200 mm x 600 mm, providing a comfortable treatment surface while saving clinic space.
Yes. The JYZ-IIB can store and recall up to 20 different treatment plans, which simplifies repeated clinical protocols and improves workflow efficiency.
Yes. The device is CE certified and meets MOL safety standards, indicating compliance with relevant international safety and quality regulations.
Accessory inclusion can vary by supplier or package. Check the specific product listing or contact the vendor to confirm which accessories are supplied with your purchase.
Warranty terms, training, and technical support are provided by the manufacturer or authorized distributor. Contact your supplier or the manufacturer's customer service for details on warranty coverage, training options, and authorized service centers.
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