Product performance

1) Timing Function

The setting range for timing is 1 to 99 minutes, with a step increment (decrement) of 1 minute. The default setting value upon startup is 20 minutes, and the timing error is ≤ ±10%.

2) Magnetotherapy Function

The treatment intensity of magnetotherapy is divided into 2 levels: weak level 3mT to 9mT, and strong level 10mT to 17mT.

Magnetic field frequency: 50Hz ± 2%

Micro-vibration Function: 4 levels of intensity are available

3) Electrotherapy Function

Main pole waveform parameters

The setting and display range of the output intensity of the main pole is 0 to 80 levels.

Direct current: Main pole basic frequency (main pole intensity: 80 levels, load 500Ω)

Auxiliary pole waveform parameters

The auxiliary pole output is represented by the numbers 01 to 10 for different biomimetic current modes, and the setting and display range of the output intensity is 0 to 90 levels.

4) Continuous working time is more than 8 hours

Scope of Application

Electrotherapy section: For assisting the functional recovery of patients with stroke and paralysis.

Magnetotherapy section: Applicable for the auxiliary treatment of ischemic cerebrovascular diseases and brain injury-related disorders.

Must-read for users

 Patients using implantable electronic devices (such as cardiac pacemakers) should not use this device without a doctor's prescription;

 When high-frequency surgical equipment and this device are connected to the same patient at the same time, there may be burns or damage to this device at the electrode of this device;

 When using this device near short-wave or microwave equipment (such as 1m), the output of this device may become unstable;

 Using the electrode of this device close to the chest will increase the risk of cardiac fibrillation;

 The maximum allowable open-circuit peak output of the electrode of this device is ≤ 200V.

 Installation of the instrument must be carried out by personnel with professional installation skills or those who have received training on instrument installation from the company.

 The operators of the instrument must have received safety, installation and operation skills training, possess proficient operation skills and strong safety awareness, and also have basic knowledge of human anatomy and medicine.

 Before treating a patient, it must be informed to the patient that during the treatment, there will be a tingling sensation from needle insertion at the treatment site, and the stronger the sensation, the better the effect.

 For patients receiving treatment for the first time, if they are nervous, it will lead to a decrease in physical tolerance, and the selected electrical stimulation intensity will be lower.

This is a normal phenomenon. After the patient adapts, gradually increase the treatment intensity, and the effect will be better.

 Because the current density of the electrode of this treatment instrument exceeds 2mA(r.m.s)/cm2, when adjusting the intensity of the electrical stimulation, it should start from the minimum and be adjusted slowly according to the patient's tolerance, and the density of the electrode current should not be increased too quickly or excessively to prevent accidents. If the patient has adapted to the current stimulation intensity, the intensity of the electrical stimulation output can be appropriately adjusted with the patient's consent.

 Postpartum patients who have not eaten, those with insufficient sleep, those with nervousness, or those with depression will affect the treatment.

 When using the treatment probe electrode, it must be firmly adhered to the treatment site. Otherwise, the patient will have a strong needle prick sensation during the treatment.

 When powered on, the electrodes of the two treatment probes cannot be combined.

 Any components of this machine are dedicated equipment for this treatment instrument. Users are not allowed to disassemble, modify or use it for other purposes without warranty coverage.

 The connection line of the treatment probe of this treatment instrument is a dedicated line. Please hold the plug to pull out or insert the treatment probe. It must be inserted or pulled out when the treatment is paused.

 During treatment, the electrode of the treatment probe must be firmly adhered to the treatment site. Before use, wipe the skin with normal saline or alcohol cotton swabs to make the contact better.

 It is strictly prohibited to pull out or insert the power plug of the instrument when the power is not turned off. The instrument should not be frequently turned on and off. If it needs to be turned on immediately after being turned off, it should wait for at least 1 minute before turning it on to avoid damaging the instrument.

Operation Procedure:

Power on preparation → Electrode connection / Wear the treatment cap → Select the treatment time for magnetic therapy and electrical therapy separately → Choose the electrical therapy plan → Start → Set the magnetic therapy parameters (magnetic field strength, vibration strength and frequency) / Set the electrical therapy parameters (brain electricity and limb) → Treatment → Treatment completion.

Power on preparation:

First, connect the output lines (brain electricity and limb) / the treatment cap to the main unit, then connect the power supply, turn on the power switch, and power on the treatment instrument. The treatment instrument is in a ready state; operate each button, the functions are normal, and the preparation is complete.

Electrodes and treatment cap connection

1) Usage method of electrodes

① Electrode connection: First, clean the treatment area with normal saline or alcohol cotton balls. Wait until the saline or alcohol dries, then attach the electrodes. Connect the output line to the electrodes and fix them with a bandage

② Electrode placement: The main electrode (for brain electricity) is placed behind the ears and at the mastoid process, Fengchi or Sunmen points; the auxiliary electrode (for limbs) is placed at the motor nerve points or Ah-shi points of the muscle tissues.

③ Treatment mode selection: Depending on different treatment needs, either the main electrode (for brain electricity) or the auxiliary electrode (for limbs) can be used for treatment alone, or the main and auxiliary electrodes can be combined for treatment.

Note: The gray electrode line is for the main electrode (brain electricity) output, and the white electrode line is for the auxiliary electrode (limbs) output. It is strictly prohibited to use the main electrode for treatment on the body or trunk, and the auxiliary electrode should be used for treatment on the head; otherwise, the treatment effect will be affected.

2) Usage instructions for the treatment cap:

When wearing the treatment cap, place the side with the plug connection line at the front end of the head, the longest connection line's electromagnetic induction treatment body at the back of the occipital region, and the remaining treatment heads evenly distributed above the temporal ear and at the top of the head. Adjust the elastic band to fix the treatment heads, and stop when the patient does not feel any urgent discomfort.

Note: When wearing the treatment cap, also put on a disposable medical cap (to prevent cross-infection). The medical cap is a disposable consumable item. Users are required to choose products with a medical device filing certificate/registration certificate for use in combination.

Treatment duration: 20-30 minutes per session, 1-2 times per day. Course of treatment: 10 sessions constitute one course. For chronic diseases, it is recommended to discontinue the treatment for 3-5 days after one course is completed before starting the next course of treatment.

Package includes:

1* Host machine

1* Treatment cap

1* Electroencephalogram output cable

1* Muscle output cable

1* Power cord

1* User manual

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