Therapy Equipments · Ultrasonic Therapy
The LCD Ultrasonic Therapy 1 MHz & 3 MHz machine is a computerised desktop unit that delivers ultrasonic therapy at two selectable frequencies through separate dedicated output ports. The 1 MHz probe addresses deep tissue structures including muscles, tendons, and joints, while the 3 MHz probe targets superficial soft tissue. Both probes connect to the unit simultaneously, with frequency selection managed via the front-panel Frequency button. The LCD screen provides a clear, real-time view of all treatment parameters. Five tactile front-panel buttons control intensity, mode, frequency, and session start/stop. The built-in digital timer supports accurate session duration management, ensuring reproducible treatment delivery across all clinical protocols.
All treatment parameters including intensity, mode, frequency, and timer are shown simultaneously on the LCD screen for clear, at-a-glance session monitoring.
Dedicated labelled output sockets for each probe frequency enable both probes to remain connected simultaneously, with the active probe selected via the front-panel Frequency button.
Two dedicated intensity buttons allow precise incremental adjustment of output intensity during treatment without the need to disconnect or reposition the probe.
The Mode button cycles through available output modes (continuous, pulse A, pulse B), enabling the clinician to match the stimulation waveform to the clinical indication.
Toggles the active output between the connected 1 MHz and 3 MHz probes, allowing swift frequency change mid-session without disconnecting cables or powering off.
A dedicated Start/Stop button initiates and pauses the treatment session and timer, supporting safe session management without altering set parameters.
The integrated session timer counts and displays treatment duration on the LCD, enabling accurate and reproducible session length management across all treatment protocols.
The compact, rounded-edge desktop housing is designed for physiotherapy treatment tables and clinic environments, with probes conveniently mounted on either side of the unit.
| Device type | Computerised LCD Ultrasonic Therapy Unit |
| Frequencies | 1 MHz and 3 MHz (separate dedicated output ports) |
| Treatment modes | Continuous, Pulse A, Pulse B (selectable) |
| Intensity control | Adjustable via up/down buttons; displayed on LCD |
| Display | LCD digital display (intensity, mode, frequency, timer) |
| Timer | Built-in digital timer (displayed on LCD) |
| Output ports | 1 × 1 MHz port and 1 × 3 MHz port (labelled) |
| Power supply | AC 110V (220V version available on request) |
| Enclosure | Compact desktop unit with rounded housing and side probe holders |
| Intended environment | Professional physiotherapy and rehabilitation clinical settings |
| Control | Function |
|---|---|
| LCD display | Shows all current treatment parameters simultaneously: intensity level, selected mode, active frequency, and session timer |
| Intensity up button | Increases the ultrasonic output intensity in incremental steps |
| Intensity down button (Timer) | Decreases the ultrasonic output intensity; also used for timer adjustment in applicable modes |
| Mode button | Cycles through available treatment modes: Continuous, Pulse A, and Pulse B |
| Frequency (FREQ) button | Switches the active output between the 1 MHz and 3 MHz probe ports |
| Start/Stop (S/S) button | Initiates or pauses the treatment session and timer countdown |
| 1 MHz output port | Dedicated socket for connecting the 1 MHz ultrasound treatment probe |
| 3 MHz output port | Dedicated socket for connecting the 3 MHz ultrasound treatment probe |
| Mains power | AC 110V mains power connection at the rear of the unit |
| Condition / Area | Application / Protocol |
|---|---|
| Musculoskeletal pain | 1 MHz for deep muscle and joint pain; 3 MHz for superficial soft tissue; continuous or pulsed mode per clinical stage |
| Soft tissue injuries | Pulsed mode (A or B) for acute and sub-acute ligament, tendon, and muscle injuries to minimise thermal effect |
| Tendinopathy and tendinitis | 1 MHz for deep tendons (Achilles, rotator cuff); 3 MHz for superficial tendons; pulsed in acute, continuous in chronic |
| Scar tissue management | 3 MHz probe with continuous mode for superficial scar softening and remodelling |
| Shoulder and neck conditions | 1 MHz for periarticular and capsular tissue; pulsed mode in acute presentations |
| Knee and hip pathology | 1 MHz for joint capsule, ligament, and periarticular soft tissue conditions |
| Plantar fasciitis | 1 MHz applied to the plantar fascia insertion; pulsed mode for acute pain, continuous for chronic stiffness |
| Sports injury rehabilitation | Frequency and mode guided by tissue depth and healing stage under physiotherapist prescription |
The LCD Ultrasonic Therapy 1 MHz & 3 MHz machine is ISO & CE marked, confirming compliance with applicable European medical device directives for safety and electromagnetic compatibility. ISO & CE documentation is available on request for regulatory submissions, hospital procurement processes, and import clearance.
plug the 1 MHz probe cable into the 1 MHz output port and the 3 MHz probe cable into the 3 MHz output port on the front panel.
apply an adequate layer of ultrasound coupling gel to the patient's skin at the treatment site before placing the probe.
press the FREQ button to select either 1 MHz (for deep tissue) or 3 MHz (for superficial tissue) according to the clinical prescription.
press the MODE button to select Continuous, Pulse A, or Pulse B as required by the treatment protocol.
use the Intensity up/down buttons to increase the output level to the prescribed therapeutic intensity as shown on the LCD display.
set the session duration using the Timer function as directed by the clinician.
Always use under professional guidance. Clinical note: all treatment parameters must be selected and supervised by a qualified physiotherapist or licensed healthcare professional. Always keep the probe in continuous movement during active output. Never hold the probe stationary on the patient's skin as this may cause localised tissue heating and periosteal burns.
Clinical settings
Suitable for
B2B distribution
✓ Handle the unit and probes with care; avoid dropping or subjecting the probe heads to mechanical shock which can damage the piezoelectric crystal. ✓ Place the unit on a stable, flat, dry surface during use and ensure cables are routed to prevent trip hazards. ✓ Inspect both probe cables, connectors, and output ports before each clinical session. ✓ Store probes with cables loosely coiled; never wrap cables tightly around the probe handle. ✓ Store the unit in a cool, dry environment away from direct sunlight and moisture when not in use.
✓ Connect to the correctly rated mains supply (AC 110V or 220V) matching the unit's specification. ✓ Never operate with a damaged power cable, plug, or probe cable. ✓ Switch off and disconnect from mains before connecting or disconnecting probe cables. ✓ Do not use in wet environments or where liquid spillage may contact the device. ✓ Do not open the unit casing; refer all internal servicing to qualified biomedical engineers only.
âš Always keep the probe in slow, continuous circular movement during active output; a stationary probe will cause localised heating and tissue burns. âš Confirm adequate coupling gel is applied before starting; reapply if the LCD display shows a warning or if the probe loses skin contact. âš Increase intensity gradually from zero; never apply maximum intensity immediately at the start of a session. âš Stop treatment immediately if the patient reports burning, sharp pain, or unusual heat at the treatment site. âš Do not treat over areas where the patient cannot reliably report sensation, as thermal damage may occur without warning.
Wipe both probe heads with a clean, soft cloth after each patient use to remove coupling gel; do not immerse probes in liquid. ✓ Clean the unit casing with a cloth lightly dampened with a mild disinfectant; do not allow liquid to enter the LCD screen, buttons, or output ports. ✓ Inspect probe faces regularly for chips, cracks, or pitting; a damaged probe face must be replaced before further clinical use. ✓ Schedule periodic output calibration and safety testing by a qualified biomedical engineer in line with local clinical device standards. ✓ Maintain a service log recording calibration dates, probe inspections, faults, and corrective actions.
Regulatory notice: this device is for professional clinical use only. It must be operated, maintained, and stored in compliance with local medical device regulations. Output calibration should be verified periodically as per local clinical engineering standards. Always follow the instructions provided in the supplied user manual and consult your regional regulatory authority for applicable compliance and registration requirements.
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LCD Ultrasonic Therapy 1 MHz & 3 MHz machine
Device type: Computerised LCD Ultrasonic Therapy Unit
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LCD Ultrasonic Therapy 1 MHz & 3 MHz machine
LCD Ultrasonic Therapy 1 MHz & 3 MHz machine