Professional Use Information for TheraMod Devices

Key Takeaways

Professional use information sets out who TheraMod rehabilitation equipment is for. TheraMod (M) Sdn. Bhd. manufactures equipment for trained clinical settings. It is not consumer equipment and it is not sold to the public.

Who the Equipment Is For

TheraMod devices are supplied to chiropractors, physiotherapists, clinics, hospitals and specialist rehabilitation centers. The user is expected to be a healthcare professional trained for the setting.

Distributors are expected to hold the regulatory permissions their own country requires.

Intended Use

Each device has a defined intended use recorded in its registration. A device should be used only within that intended use. Clinical judgment remains with the treating professional.

Training

Equipment is supplied with professional-user training. Training covers setup, positioning, operation, documentation and safe handling. TheraMod does not supply equipment without a training pathway.

Installation and Service

Installation is planned before delivery. Room access, power, floor loading and workflow are reviewed first. Service planning and spare-part supply are agreed with the distributor.

Documentation

Each device is supplied with user documentation. Registration and certificate references are provided on request to qualified buyers and distributors.

The Settings the Equipment Is Built For

TheraMod builds for rooms where workflow matters. That means controlled patient positioning, clear table access, readable controls and records that can be kept.

Typical settings include chiropractic clinics, physiotherapy departments, hospital rehabilitation units and specialist spine centers. Each setting has different space, power and staffing needs. Those are reviewed before an order is confirmed.

What a Buyer Should Check First

• Whether the intended use matches the care your clinic provides.
• Whether your staff hold the training the device requires.
• Whether the room can take the equipment safely.
• Whether the device is registered in your own country.
• Who will service the equipment locally.

Regulatory Record

Registration and certification are regulatory and quality-system facts. They do not establish clinical outcomes, comparative superiority, authorization in another market, or MDA endorsement.

What This Page Does Not Say

• It does not claim a treatment result.
• It does not compare TheraMod equipment with any other equipment.
• It does not state that a device is approved outside Malaysia.
• It does not replace the documentation supplied with a device.

Requesting Professional Information

Qualified buyers and distributors can request specifications, installation requirements and training details through the TheraMod contact page or by writing to [email protected].

The three current devices are RxDecom®, Spinercise® and FD-3000™. The full range is set out on the rehabilitation device portfolio page.

Related Pages

• RxDecom® spinal decompression machine. The registered Class A controlled spinal distraction device.
• Spinercise® rehabilitation device. The registered movement-based rehabilitation device.
• FD-3000™ flexion distraction device. The registered flexion distraction rehabilitation device.
• Rehabilitation device portfolio. All three registered devices in one place.
• Terms of use. The terms that govern use of this website.
• Spinal decompression therapy equipment. What the equipment category is and what the evidence says.
• Spinal traction compared with decompression. How the two equipment categories differ.

Last Updated and Reviewed

“Professional Use Information for TheraMod Devices” was reviewed and updated on 1 September 2026 by Yama Zafer, D.C., Founder and Managing Director of TheraMod (M) Sdn. Bhd.

Author

Yama Zafer, D.C., author of “Professional Use Information,” is the Founder and Managing Director of TheraMod (M) Sdn. Bhd.; read his TheraMod corporate biography.