Cervical and Lumbar Traction Device and Spine Traction Bed and Orthopedic Traction Table

The JYZ-IIB is a microcomputer-controlled, three-dimensional multifunctional traction bed designed for integrated cervical and lumbar traction. It uses a telescopic motor for traction drive and offers multiple automated traction programs for clinical use.

The device is suitable for cervical and lumbar traction therapy, typically used in orthopedic and rehabilitation settings for spinal decompression and related treatments. Specific diagnoses and treatment plans should be determined by a qualified clinician.

The bed provides eight built-in traction methods (including intermittent, sustained, repeated, and up/down ladder variations) and supports 20 memory treatment plans for convenient clinical operation.

Safety features include microcomputer program control of time and force, an emergency stop switch for the patient, and preset limits for traction parameters. Operators should follow the user manual and clinical protocols during use.

Contraindications include severe heart, brain, or lung disease; bleeding disorders; severe local skin disease; infectious spinal conditions (e.g., spinal tuberculosis, osteomyelitis), bone tumors, severe osteoporosis, acute spinal injury with cord symptoms; pregnancy beyond three months; intoxication or extreme weakness; and severe uncontrolled hypertension. Mild hypertension patients should limit session duration. Clinician screening is required.

Cervical traction stroke: 0–300 mm; cervical traction force: 0–300 N; angle action range: -10° to +30°. Exact applied parameters should be set per patient needs and clinical guidance.

Lumbar traction stroke: 0–300 mm; lumbar traction force: 0–990 N. Stroke and force are adjustable within these ranges under program control.

Total traction time can be set from 0 to 99 minutes, traction time 0–9 minutes, intermittent time 0–9 minutes, and training time 1–90 minutes. The microcomputer allows automated program cycles including intermittent and sustained modes.

Bed dimensions are 1200 mm (L) × 600 mm (W). Recommended ambient operating temperature range is +5°C to +40°C.

Rated voltage: AC 220 V, 50 Hz. Rated input power is 80 VA. Confirm local electrical compatibility before installation.

Yes. The device should be operated only by trained clinical personnel who understand traction therapy indications, contraindications, and the unit's controls. Follow local clinical protocols and the manufacturer’s user manual.

Unplug the device before cleaning. Wipe surfaces with a soft, damp cloth and mild disinfectant compatible with the upholstery and avoid wetting motors or electrical components. Perform regular inspections of cables, motors, and fasteners and arrange qualified servicing if faults are detected. Follow the manufacturer’s maintenance schedule in the manual.

The listed MOQ is 1 set. Accessory inclusions (e.g., harnesses, straps, power cord) and packaging contents vary by supplier—confirm with the vendor or sales representative for a complete list.

Warranty terms, after-sales service, and technical support are provided by the manufacturer or authorized dealer. Contact your supplier for warranty details, service agreements, and authorized service centers.

Continuously observe the patient for discomfort, neurological changes, or vital sign instability. Ensure the patient knows how to use the emergency stop. Adjust or terminate treatment if adverse symptoms occur, and document the session according to clinical protocols.