Therapy Equipments · Electrotherapy
This digital interferential therapy unit combines IFT and muscle stimulation in a single desktop device, providing physiotherapy clinicians with a versatile platform for pain management, muscle re-education, and rehabilitation. Programme selection, digital displays per parameter, selectable carrier frequencies, and multiple beat frequency modes give clinicians precise control over every aspect of treatment. The unit supports 2-pole, 4-pole vector, and 4-pole treatment modes, making it suitable for both small targeted areas and larger anatomical regions. Adjustable sweep patterns and intensity balance controls, combined with a digital timer, enable reproducible sessions across a wide range of clinical indications.
A single device supports both interferential therapy for pain modulation and muscle stimulation for motor re-education and strengthening protocols.
2 kHz and 4 kHz carrier frequency options allow the clinician to select the appropriate medium-frequency current for the treatment area and depth required.
0 to 150 Hz scan, 80 to 150 Hz, 0 to 10 Hz scan, and 0 to 100 constant provide a comprehensive range of beat frequencies for acute, sub-acute, and chronic conditions.
Selectable sweep patterns including continuous, triangular, and trapezoidal modes adapt stimulation to patient tolerance and clinical objectives.
Three electrode configuration modes support conventional bipolar application, 4-pole vector scanning for automatic current rotation, and fixed 4-pole placement.
Independent channel intensity adjustment and inter-channel balance control enable precise, patient-specific stimulation delivery across both output channels.
Multiple pre-set programmes with individual digital displays for each parameter support standardised, reproducible treatment delivery.
Dedicated start and stop controls allow the clinician to initiate and pause treatment without adjusting intensity settings, supporting safe session management.
| Device type | Digital Interferential Therapy Unit with Muscle Stimulation |
| Therapy modes | Interferential therapy (IFT) and muscle stimulation |
| Carrier frequency | 2 kHz and 4 kHz (selectable) |
| Beat frequency modes | 0 to 150 Hz scan; 80 to 150 Hz; 0 to 10 Hz scan; 0 to 100 constant |
| Sweep patterns | Multiple selectable sweep modes |
| Treatment modes | 2-pole, 4-pole vector, 4-pole |
| Output | Single output socket with channel intensity and balance controls |
| Display | Digital display per parameter with programme selection indicator |
| Timer | Digital programmable timer (minutes) |
| Power supply | Mains AC, 110V / 220V, 50/60 Hz |
| Enclosure | Metal desktop housing with front control panel |
| Intended use environment | Professional physiotherapy and rehabilitation clinical settings |
| Control | Function |
|---|---|
| Programme selector | Selects from pre-set IFT or muscle stimulation treatment programmes |
| Timer (Min) | Sets treatment session duration in minutes; displays elapsed time on digital readout |
| Intensity (CH-1 / CH-2) | Adjusts output current intensity for each of the two treatment channels independently |
| Balance control | Adjusts the relative intensity balance between channels for targeted current distribution |
| Beat frequency selector | Selects the beat frequency mode (0-150 scan, 80-150, 0-10 scan, 0-100 constant) |
| Frequency (Hz) selector | Selects carrier frequency: 2 kHz or 4 kHz |
| Sweep pattern selector | Selects the modulation sweep pattern applied to the beat frequency output |
| Treatment mode switch | Switches between 2-pole, 4-pole vector, and 4-pole electrode configuration modes |
| Start / Stop button | Initiates or pauses the treatment session without altering intensity settings |
| Output socket | Connects electrode lead cables to the patient electrodes |
| Mains power switch | Powers the unit on or off |
| Condition / Area | Application / Protocol |
|---|---|
| Acute and chronic pain management | IFT applied to modulate pain through gate control and endorphin release mechanisms |
| Post-operative pain relief | Interferential current applied peri-incisionally under clinical supervision to support analgesic management |
| Musculoskeletal conditions | Shoulder, knee, hip, and spinal conditions responsive to medium-frequency electrotherapy |
| Muscle re-education | Muscle stimulation mode used to facilitate motor relearning following injury or neurological event |
| Oedema reduction | Low beat frequency IFT to stimulate lymphatic and venous return in acute oedema under clinical guidance |
| Sports injury rehabilitation | Pain relief and muscle activation support during sports physiotherapy programmes |
| Low back and neck pain | 4-pole vector mode applied to the lumbar or cervical region for deep tissue current penetration |
| Peripheral circulatory conditions | Vasomotor stimulation to improve local circulation as part of a supervised clinical protocol |
This interferential therapy and muscle stimulation unit is CE marked, confirming compliance with applicable European medical device directives for safety and performance. CE documentation is available on request for regulatory submissions, procurement, and import clearance purposes.
Clinical settings
Suitable for
B2B distribution
✓ Handle the unit with care; avoid dropping or subjecting it to mechanical shock or vibration. ✓ Place on a stable, flat, dry surface during use and ensure ventilation slots remain unobstructed. ✓ Store in a cool, dry environment away from direct sunlight, heat sources, and moisture. ✓ Inspect all electrode cables, connectors, and the output socket before each use session. ✓ Do not place liquids on or near the unit during operation
✓ Connect to a correctly rated and earthed mains supply matching the unit's specified voltage and frequency. ✓ Never operate with a damaged power cable, plug, or electrode lead. ✓ Switch off and disconnect from mains before cleaning, servicing, or replacing electrodes. ✓ Do not use in wet environments or where liquid spillage may contact the device. ✓ Do not attempt to open the casing or carry out internal repairs; refer all servicing to qualified biomedical engineers.
âš Always increase intensity gradually from zero; never apply stimulation at high intensity immediately. âš Ensure all electrodes are firmly and correctly placed before increasing output intensity. âš Reduce all channel intensities to zero before removing electrodes from the patient at the end of a session. âš Never leave a patient unattended during active interferential or muscle stimulation treatment. âš Discontinue immediately if the patient reports burning, pain, skin irritation, or any unusual sensation.
✓ Wipe the exterior casing with a soft cloth lightly dampened with a mild clinical disinfectant after each use. ✓ Do not immerse the unit in liquid or apply spray cleaners directly onto the panel or casing. ✓ Inspect electrode lead cables and connectors regularly and replace if insulation is damaged or connectors are corroded. ✓ Schedule periodic calibration and safety inspection by a qualified biomedical engineer in line with local clinical standards. ✓ Maintain a service log recording inspection dates, faults, and corrective actions taken.
Regulatory notice: this device is for professional clinical use only. It must be operated, maintained, and stored in compliance with local medical device regulations. 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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Interferential Therapy Cum Stimulator
Device type: Digital Interferential Therapy Unit with Muscle Stimulation
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Interferential Therapy Cum Stimulator
Interferential Therapy Cum Stimulator