Therapy Equipments · Ultrasonic Therapy
The ULTR 52 Pro is an advanced digital ultrasound therapy device providing 1 MHz and 3 MHz treatment frequencies through separate labelled output ports. Three individual digital displays show session time, treatment mode, and output intensity in W/cm² simultaneously and independently, eliminating the ambiguity of combined or scrolling parameter displays. Four output modes including Continuous, Pulse A, Pulse B, and Wave cover the full spectrum of acute, sub-acute, and chronic clinical applications. Designed for home wellness and personal therapy use as well as clinical settings, the unit is straightforward to operate with logically grouped controls for Time, Mode/Selector Probe, and Intensity. Error, 1 MHz, and 3 MHz LED indicators on the right panel provide real-time system status throughout every session.
Separate green digital readouts for time (minutes), mode, and intensity (W/cm²) make it easy to monitor all session parameters simultaneously without sharing a single screen.
Continuous output delivers uninterrupted ultrasonic energy. Pulse A and Pulse B modes provide pulsed waveforms at different duty cycles. Wave mode adds a modulated output for additional clinical flexibility.
Output intensity is shown as a precise digital value in W/cm² on the right display, accompanied by a bar-graph indicator for quick visual reference during active probe application.
Three right-panel LEDs confirm active probe frequency, alert to poor acoustic coupling or disconnected probes via the Error LED, and provide instant system status feedback throughout treatment.
The Selector Probe button on the Mode panel switches the active output between the connected 1 MHz and 3 MHz probes without powering off or reconnecting cables.
Dedicated up and down buttons on the Time panel allow session duration to be set and adjusted in the unit of minutes, with the countdown shown on the left digital display.
Separate intensity up and down buttons on the right panel provide precise incremental adjustment of output level during active treatment without requiring probe lift-off.
The ULTR 52 Pro is specifically designed for home wellness and personal therapy applications in addition to clinical use, with intuitive controls and clear displays suited to informed personal therapy programmes.
| Model | ULTR 52 Pro (Advanced Ultrasound Therapy 1 & 3 MHz) |
| Device type | Digital dual-frequency ultrasound therapy unit |
| Frequencies | 1 MHz and 3 MHz (separate labelled output ports) |
| Output modes | Continuous (CONT.), Pulse A, Pulse B, Wave |
| Displays | 3 separate digital displays: left (time/min), centre (mode), right (intensity W/cm²) |
| Intensity indicator | Digital W/cm² readout plus bar-graph visual indicator |
| Status LEDs | Error LED, 1 MHz LED, 3 MHz LED (right panel) |
| Probe selector | Front-panel selector probe button (Mode section) |
| Timer | Adjustable via Time up/down buttons; countdown on left display |
| Power supply | Mains AC, 110V / 220V, 50/60 Hz |
| Enclosure | Desktop unit with side probe holders |
| Intended use | Home wellness, personal therapy, and professional clinical settings |
| Control | Function |
|---|---|
| Power button | Switches the unit on or off from the mains supply |
| Time display (left) | Green digital display showing the current session timer value in minutes |
| Time up button | Increases the session duration setting |
| Time down button | Decreases the session duration setting |
| Mode display (centre) | Green digital display showing the currently active output mode |
| CONT. button | Selects continuous output mode for uninterrupted ultrasound delivery |
| PULSE A button | Selects Pulse A pulsed output mode at a defined duty cycle |
| PULSE B button | Selects Pulse B pulsed output mode at an alternative duty cycle |
| WAVE button | Selects Wave modulated output mode |
| Mode up / Mode down buttons | Navigate through mode options when using the mode buttons |
| Selector Probe button | Switches the active output between the 1 MHz and 3 MHz probe ports |
| Selector Probe left / right buttons | Navigate probe selection options |
| Intensity display (right) | Green digital display showing the current output intensity in W/cm² |
| Intensity bar graph | Visual bar indicator of relative output intensity level |
| Intensity up button | Increases the output intensity in incremental steps |
| Intensity down button | Decreases the output intensity in incremental steps |
| ERROR LED | Illuminates on poor acoustic coupling, probe disconnection, or system fault |
| 1 MHz LED | Illuminates when the 1 MHz probe is the active output frequency |
| 3 MHz LED | Illuminates when the 3 MHz probe is the active output frequency |
| 1 MHz output port | Front-panel socket for the 1 MHz probe cable connection |
| 3 MHz output port | Front-panel socket for the 3 MHz probe cable connection |
| Condition / Area | Application / Protocol |
|---|---|
| Muscle and joint pain relief | 1 MHz for deeper musculature and joints; 3 MHz for superficial muscles; continuous or pulsed as recommended by clinician |
| Soft tissue recovery | Pulse A or Pulse B modes to support tissue recovery with reduced thermal effect |
| Tendon and ligament support | 1 MHz for deep tendons; 3 MHz for superficial tendons; pulsed for acute, continuous for chronic |
| Scar tissue care | 3 MHz with continuous or Wave mode for superficial scar tissue work |
| Post-exercise muscle recovery | 3 MHz for superficial muscles with Pulse A mode under personal wellness protocol |
| Shoulder and neck wellness | 1 MHz for deeper structures; appropriate mode and intensity per clinician guidance |
| Knee and back wellness | 1 MHz probe for deeper soft tissue support in the knee and lumbar region |
| Plantar fascia care | 1 MHz at the plantar fascia region; intensity and duration per clinician-approved personal protocol |
The Digital Ultrasound Device 1-3MHz 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, procurement, and import clearance purposes.
Home and personal use
Clinical settings
B2B distribution
✓ Handle probe heads with care; avoid dropping or mechanical shock as this can damage the piezoelectric crystal. ✓ Place the unit on a stable, flat, dry surface during operation and route cables to prevent trip hazards. ✓ Inspect both probe cables, connectors, and front-panel output ports before each use session. ✓ Store probes in the side holders provided; never tightly wrap cables around probe handles. ✓ Store the unit in a cool, dry environment away from direct sunlight when not in use.
✓ Connect to a correctly rated mains supply (110V or 220V) matching the unit's label specification. ✓ Never operate with a damaged power cable, plug, or probe cable; replace before use. ✓ Switch off and disconnect from mains before connecting or disconnecting probe cables. ✓ Do not use near water or in wet environments; keep all liquid away from the unit, displays, and ports. ✓ Do not open the unit casing; refer all servicing to qualified technical personnel.
âš Always keep the probe in slow, continuous movement during active output; a stationary probe causes tissue burns and periosteal damage. âš If the ERROR LED illuminates during treatment, stop immediately and check coupling gel coverage and probe connection before resuming. âš Always start at the lowest intensity setting and increase gradually; never begin at high intensity. âš Stop use immediately if burning, sharp pain, or unusual heat is experienced at the treatment site. âš Do not treat areas of impaired sensation, open wounds, or infections; do not self-treat undiagnosed conditions.
✓ Wipe probe heads with a clean, soft cloth after each use to remove coupling gel; do not immerse probes in liquid. ✓ Clean the unit casing with a lightly dampened cloth; do not allow liquid to enter any display, button, or port. ✓ Inspect probe faces for chips or pitting; a damaged probe face should be replaced before further use. ✓ For clinical use, schedule periodic output calibration and safety checks per local device maintenance standards. ✓ Keep a record of usage sessions, any faults noted, and maintenance actions taken.
Regulatory notice: this device is CE marked for use in home wellness and personal therapy as well as clinical settings. It must be operated, maintained, and stored in compliance with applicable local regulations. Always read the supplied user manual fully before first use. Consult a qualified healthcare professional before self-treating any injury, pain, or medical condition.
Questions
Leave your details and we'll call you back about Digital Ultrasound Device 1-3MHz Pain Relief Machine.
Digital Ultrasound Device 1-3MHz Pain Relief Machine
Model: ULTR 52 Pro (Advanced Ultrasound Therapy)
Prefer a call instead? Request a callback
In order to provide you a personalized shopping experience, our site uses cookies. By continuing to use this site, you are agreeing to our cookie policy.
Don't have an account yet? Sign up
No items in your cart. Go on, fill it up with something you love!
Start Shopping Now
Digital Ultrasound Device 1-3MHz Pain Relief Machine
Digital Ultrasound Device 1-3MHz Pain Relief Machine