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Lumbar traction

I have found results from4000+products and2000+suppliers aboutLumbar traction

Commonly Used:
US$
Customization Available
Sample Available
Manufacturer First
Product Attributes:
Type: Orthopedics
Type: Ophthalmology
Certification: CE
Group: Adult
Function: Analgesia
Medical Device Regulatory Type: Type 2
With LCD Display
Exercise Part: Waist
Application: Home
Age: Adult
Folded: Unfolded
Color: Black
Condition: New
Customized: Customized
Theory: Electrotherapeutics
Seater: 1
Rotary: Fixed
Armrest: Without Armrest
Fixed: Unfixed
Padding: High-density Foam
Suitable for: Adult
Certification: FDA
Certification: ISO13485
Certification: ISO
Function: Tissue Repair
Improve Blood Circulation
Function: Biological Regulatio
Without LCD Display
Folded: Folded
Color: Blue
Theory: Ultrasonic
Theory: Radial

Sourcing guidance for Lumbar Traction

What are the key technical specifications to consider when sourcing lumbar traction devices?

Buyers should prioritize traction force range (typically 0-99kg for clinical grade) and adjustment precision. For electronic models, ensure the presence of multi-mode settings (continuous, intermittent, and pulse) and integrated heat therapy features. The material of the traction belt must be high-tensile, medical-grade nylon or reinforced PU to prevent stretching or tearing under high pressure.

Which international compliance standards are mandatory for lumbar traction equipment?

As medical devices, these products must adhere to ISO 13485 (Medical Devices Quality Management Systems). For the US market, FDA Class I or II registration is required, while the EU market necessitates CE Marking (MDR 2017/745). Ensure the supplier provides RoHS and REACH certifications for all skin-contact materials to avoid toxic chemical exposure.

How can I evaluate the safety features of automated lumbar traction machines?

Safety is paramount. Verify the inclusion of an emergency stop switch accessible to the patient. The device should have over-pressure protection and an automatic pressure release function in case of power failure. For home-use inflatable belts, check for anti-burst valves that prevent over-inflation beyond the recommended PSI.

What are the common usage scenarios and target markets for these products?

Products range from professional clinical units for physiotherapy centers to portable inflatable belts for home care and ergonomic stretchers for office workers. Identifying your target segment is crucial; clinical units require higher durability and certification, while consumer-grade portables focus on lightweight design and ease of use.

Cross-Border Procurement Risks and Strategies

How can I mitigate quality risks when purchasing from overseas suppliers?

Always request a pre-shipment inspection (PSI) by a third-party agency like SGS or Intertek. Focus on load-bearing tests and electrical safety leakage tests. For large orders, use Made-in-China.com's Secured Trading Service to ensure payment is only released after the goods pass quality verification.

What are the best practices for negotiating with medical equipment suppliers?

Negotiate based on Total Cost of Ownership (TCO) rather than just the unit price. Ask for spare parts (e.g., extra belts, remote controls) to be included at no cost (usually 2-3% of order volume). Request a warranty extension to 24 months for core components like motors or air pumps to ensure long-term ROI.

What shipping precautions should be taken for sensitive traction electronics?

Lumbar traction devices often contain sensitive sensors and motors. Insist on double-walled corrugated export packaging with custom-fit EPE foam inserts. For sea freight, ensure the use of desiccant silica gel packs inside the polybags to prevent moisture damage and mold during long-transit periods.

How do I handle customs clearance for medical-related traction devices?

Ensure the HS Code (typically 901910) is correctly declared. Provide the supplier with a detailed packing list and commercial invoice that matches your local customs requirements. If you are importing to the US, ensure the supplier has a valid FDA 510(k) number or listing to avoid shipment seizure at the border.

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