PHYSIPOD MT8000 Instruction Manual

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INSTRUCTION MANUAL

MULTI MODALITY

ELECTRICAL STIMULATOR

INTERFERENTIAL | TENS | EMS | MICROCURRENT

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Table of Contents

1.Safety information…..………………………………………..

1.1 General description

1.2 Medical background

1.3 Indication for use

1.4 Contraindications

1.5 Warnings, Cautions, Adverse Reactions

2. Presentation ……………………………………………...… 13

2.1 Front and Rear panel

2.2 LCD display

3. Specification…………………………………………………

3.1 Accessories

3.2 Technical information

3.3 The waveforms of the stimulation programs

4. Instruction for use …………………………………………..

4.1 Battery

4.2 Connect electrodes to lead wires

4.3 Connect lead wires to device

4.4 Electrode

4.5 Turn ON

4.6 Select the Therapeutic Mode

4.7 Steps to set a new program

4.8 Adjust Channel Intensity

4.9 Lock the button

4.10 Stop the treatment

4.11 Turn OFF

4.12 Low battery indicator.

5. Program……………………………………………………….36

6. Cleaning and Care………………………………………….. 37

6.1 Tips for skin care

6.2 Cleaning the device

6.3 Electrodes

6.4 Cleaning the Electrodes cords

6.5 Maintenance

7. Troubleshooting…………………………………………......41

8. Storage……………………………………………………….. 42 9 .Disposal……………………………………………………….43

10. Electromagnetic Compatibility (EMC) Tables……….....43

11. Glossary symbols…………………………………...........

12. Warranty…………………………………………………..…49

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1. Safety information

1.1 General

M T 8 0 0 0 E l e c t r i c a l S t i m u l a t o r i s a p or ta bl e electrotherapy device featuring four therapeutic m o d e s : Tr an sc ut an e o u s E l e c t r ic al Ne rv e

S t i m u l a t o r , E l e c t r i c a l M us cl e S t i m u l a t i o n Interferential, and Microcurrent,which are used for

pain relief and electrical muscle stimulation. The sti m ulator sends ge n tle el ectrica l curr ent to underlying nerves and muscle group via electrodes applied on the skin. The parameters of device are controlled by the press buttons. Its intensity level is adjustable according to the needs of patients.

EXPLANATION OF TENS

Transcutaneous Electrical Nerve Stimulation (TENS) is a non-invasive, drugfree method of controlling pain. TENS uses tiny electrical impulses sent through the skin to nerves to modify your pain perception. TENS does not cure any physiological problem; it only helps control the pain. TENS does not work for everyone; however, in most patients it is effective in reducing or eliminating the pain, allowing for a return to normal activity.

EXPLANATION OF EMS

E l e c tr i c a l M u sc l e S t i m u l a ti o n ( E M S ) i s a n internationally accepted and proven way of treating muscular injuries. It works by sending electronic pulses to the muscle needing treatment; this causes

1.2 Medical background

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the muscle to exercise passively. It is a product derived from the square waveform (ladder-sha ped). Through the square wave pattern it is able to work dire ctly on muscle motor neurons. This device has low frequency and this in conjunction with the square wave pattern allows direct work on muscle groupings. This is being widely used in hospitals and sports clinics for the reatment of muscular injuries and for the re-education of paralyzed muscles, to prevent atrophy in affected muscles and improving muscle tone and blood circulation.

EXPLANATION OF IF

Interferential Stimulation (IF) is an anti-inflammatory based treatment modality. Interferential stimulation is characterized by two alternating-current sine waves or square waves of differing frequencies that “work” together to produce an interferential current that is also known as a beat pulse or alternating modulation frequency. One of the two currents is usually held at 4,000 Hz, and the other can be held constant or varied over a range of 4,001 to 4,100 Hz. Because of the frequency, the interferential wave meets low impedance when crossing the skin to enter deep into soft tissues. The interferential currents reportedly can stimulate sensory, motor, and pain fibers. These large impulse fibers interfere with the transmission of pain messages at the spinal cord level. This deep tissue penetration stimulates parasympathetic nerve fibers for increased blood flow and edema reduction. It utilizes the low electric-current to stimulate muscle nerves to achieve the symptomatic relief of chronic intractable pain, post-traumatic pain, and postsurgical pain.

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EXPLANATION OF MICROCURRENT

Microcurrent stimulation is a type of therapy in which very low current is sent into the cells of the body. Microcurrent is a very faint current that is so small it is measured in millionths of an amp (Microamps). Human cells generate a current that is in the microamp range which is why you can't feel it-the current is so low it doesn't stimulate the sensory nerves.

Microcurrent is a physiological electric modality that increases ATP (energy) production in the cells of your body. This dramatically increases the tissue's healing rate. The i mmediate respons e t o the corr e c t m i c r oc ur r e n t f r e q u e nc y s u gg es t s t ha t o t h e r mechanisms are involved as well. The exact effects or changes in the tissue are unmistakable; scars will often suddenly soften; trigger points often become less painful within minutes when the “correct” frequency is applied. In many situations the changes seen seem to be long lasting and in many cases permanent.

1.3 Indication for use

MT8000 electrical stimulator may be used for the following conditions:

1) Symptomatic relief of chronic intractable pain; Post traumatic pain; post surgical pain.

2) Relaxation of muscle spasm.

3) Increase of blood flow circulation

4) Prevention or retardation of disuse atrophy

5) Muscle re-education

6) Maintaining or increasing range of motion.

7) Immediate post-surgical stimulation of calf muscles to prevent venous thrombosis

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IMPORTANT SAFETY INFORMATION!

Read instruction manual before operation. Be sure to comply with all “Contraindications”, Warnings”, “Cautions” and “Adverse reactions” in the manual. Failure to follow instructions can cause harm to user or device.

1.4 Contraindications

1) This device should not be used for symptomatic local pain relief unless etiology is established or unless a pain syndrome has been diagnosed.

2) This device should not be used when cancerous lesions are present in the treatment area.

3) Stimulation should not be applied over swollen, infected, inflamed areas or skin eruptions (e.g. phl ebitis, thrombophlebitis, varicose veins, etc.).

4) Electrodes must not be applied to sites that might cause current/stimulation to flow through the carotid sinus region (anterior neck) or transcerebrally (through the head).

5) Do not use this device if the patient has a demand type cardiac pacemaker or any implanted defibrillator.

6) This device should not be used over poorly enervated areas.

7) Epilepsy

8) Serious arterial circulatory problems in the lower limbs

9) Abdominal or inguinal hernia

10) Do not use this device if you have heart disease without consulting your physician.

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1.5 Warnings, Cautions and Adverse Reactions

WARNINGS:

1) This device should be used only under the continued supervision of a licensed physician.

2) The long-term effects of chronic electrical stimulation are unknown. Electrical stimulation devices do not have any curative value .

3) TENS is a symptomatic treatment and, as such, suppresses the sensation of pain, which would otherwise serve as a protective mechanism.

4) Safety has not been established for the use of therapeutic electrical stimulation during pregnancy. Do not use during pregnancy unless directed by your physician.

5) Electrical stimulation is not effective for pain of central origin.

6) Electronic monitoring equipment (such as ECG monitors and ECG alarms) may not operate properly when electrical stimulation is in use.

7) Stimulation should not be applied over the carotid sinus nerves, particularly in patients with a known sensitivity to the carotid sinus reflex.

8) Stimulation should not be applied over the neckor mouth. Severe spasm of the laryngeal and pharyngeal muscles may occur and the contractions may be strong enough to close the airway or cause difficulty in breathing.

9) Stimulation should not be applied transthoracically in that the introduction of electrical current into the heart may cause cardiac arrhythmias.

10) Stimulation should not take place while the user is connected to high-frequency surgical equipment, it may cause burn injuries on the skin under the electrodes, as well as problems with the stimulator.

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11) Do not use the stimulator in the vicinity of shortwave or microwave therapy equipment, since this may affect the output power of the stimulator.

12) Never use in environments with high humidity such as in the bathroom or when having a bath or shower.

13) Caution should be used in applying electrical stimulation to patients suspected of having heart disease. Further clinical data is needed to show there are no adverse results.

14) Never use near the heart. Stimulation electrodes should never be placed anywhere on the front of the thorax (marked by ribs and breastbone), but above all not on the two large pectoral muscles. Here it can increase the risk of ventricular fibrillation and lead to cardiac arrest.

15) Electrodes should not be placed over the eyes, in the mouth, near the genitals or internally.

16) Never use on the areas of the skin which lack normal sensation

17) Apply the electrodes to clean, dry, and unbroken skin only.

18) Keep electrodes separate during treatment, electrodes in contact with other could result in improper stimulation or skin burns.

19) Keep the stimulator out of reach of children.

20) Consult your doctor if you are in any doubt whatsoever.

CAUTIONS:

1) Federal law (USA) restricts this device to sale by or on the order of a physician.

2) For single patient use only.

3) Keep yourself informed of the contraindications.

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4) This stimulator not intended for unattended, personal use by patients who have noncompliant, emotionally disturbed, dementia, or low IQ.

5) Read, understand, and practice the warnings, cautions and operating instructions. Know the limitations and hazards associated with using any device. Observe the precautionary and operational decals placed on the unit. Always follow the operating instructions prescr ibed by your healthcare practitioner.

6) The instruction of use was listed; any improper use may be dangerous.

7) Do not use this device for undiagnosed pain syndromes until consulting a physician.

8) Patients with an implanted electronic device, such as a cardiac pacemaker, implanted defibrillator, or any other metallic or electronic device should not use this device without first consulting a doctor.

9) Stimulation delivered by this device may be sufficient to cause electrocution. Electrical current of this magnitude must not flow through the thorax or across the chest because it may cause a cardiac arrhythmia.

10) Do not place electrodes on the front of the throat as spasm of the Laryngeal and Pharyngeal muscle may occur. Stimulation over the carotid sinus (neck region) may close the airways, make breathing difficult, and may have adverse effects on the heart rhythm or blood pressure.

11) Do not place electrodes on your head or at any sites that may cause the electrical current to flow transcerebrally (through the head).

12) Patients with heart disease, epilepsy, cancer or any other health condition should not use this device without first consulting a physician.

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13) Some patients may experience skin irritation or hypersensitivity due to the electrical stimulation or silicone rubber. If rash develops or pain persists, discontinue use and consult a doctor.

14) Electrode placement and stimulation settings should be based on the guidance of prescribing practitioner.

15) Effectiveness is highly dependent upon patient selection by a person qualified in the management of pain afflicted patients.

16) Isolated cases of skin irritation may occur at the site of the electrode placement following long-term application. If this occurs, discontinue use and consult your physician.

17) The electrodes are only to be placed on healthy skin. Avoid skin irritation by ensuring that good contact is achieved between electrodes and skin.

18) If the stimulation levels are uncomfortable or become uncomfortable, reduce the stimulation Intensity to a comfortable level and contact your physician if problems persist.

19) This device should not be used while driving, operating machinery, close to water, or during any activity in which involuntary muscle contractions may put the user at undue risk of injury.

20) Never use the device in rooms where aerosols (sprays) are used or pure oxygen is being administered.

21) Do not use it near any highly flammable substances, gases or explosives.

22) Do not use this device at the same time as other equipment which sends electrical pulses to your body.

23) Do not confuse the electrode cables and contacts with your headphones or other devices, and do no t connect the electrodes to other devices .

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24) Do not use sharp objects such as pencil point or ballpoint pen to operate the buttons on the control panel.

25) Inspect Applicator cables and associated connectors before each use.

26) Turn the device off before applying or removing electrodes.

27) Electrical stimulators should be used only with the leads and electrodes recommended for use by the manufacturer

28) This device has no AP/APG protection. Do not use it in the presence of explosive atmosphere and flammable mixture.

Adverse Reactions:

1) Skin irritation from the electrode gel and electrode burns are potential adverse reactions. If skin irritation occurs, discontinue use and consult you r physician.

2) If the stimulation levels are uncomfortable, reduce the stimulation Intensity to a comfortable level and contact your physician if problems persist.

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2. Presentation

2.1 Front and Rear Panel

1) Increasing the output intensity of channel 1 [▲ . To set the application program and the parameter of the waveform in the setting state.

2) Decreasing the output intensity of channel 1 [▼]. To set the application program and the parameter of the waveform in the setting state. To unlock the current treatment program.

3) Therapeutic mode selection [M]. Stop the treatment. Exit setting mode to the user interface.

4) LCD display: Shows the operating state of the device.

5) Increasing the output intensity of channel 2 [▲]. To set the application program and the parameter of the waveform in the setting state.

6) Decreasing the output intensity of channel 2 [▼]. To set the application program and the parameter of the waveform in the setting state. To unlock the current treatment program.

]

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7) Parameter Selection [S]: press the button to enter setting state; you can select the difference parameters in conjunction with [▲] and [▼].

8) Turn OFF/ON: press the [ ]button to turn on th e device or keep [ ] button for approx.3 seconds to turn off the device.

9) Output socket: electric signal output afte r connection of the cable with adhesive electrodes channel 1

10) Output socket: electric signal output after connection of the cable with adhesive electrodes channel 2

11) Belt Clip

12) The battery compartment cover for opening

13) Adapter Receptacle

2.2 LCD display

1) Display therapeutic mode

2) Display therapeutic program or Display the cycle time for TENS, IF and MIC therapeutic mode in setting state.

3) Timer symbol

4) EMS waveform of ramp up and ramp down time

5) Display of waveform pulse width

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6) Display the channel 1

7) Display numbers of the output intensity for channel 1(CH1); Display numbers of waveform pulse width or EMS waveform of contraction (working) time in setting state.

8) EMS waveform of contraction (working) time

9) Display of waveform pulse rate

10) Display numbers of the output intensity for channel 2(CH2); Display numbers of waveform pulse rate or EMS waveform of relaxation time in setting state.

11) Low-battery indicator

12) The device is locked indicator

13) Display numbers of the treatment time or EMS waveform of ramp up and ramp down time

14) EMS waveform of relaxation time

15) Display the channel 2

3. Specification

3.1 Accessories

No DESCRIPTION Q’TY 1 Electrical stimulator device 1 piece 2 Electrodes Leads 2 pieces 3 40*40 mm Adhesive Electrodes 4 pieces 4 9V Battery, type 6LR61 1 piece 5 Instruction Manual 1 piece 6 Carrying case 1 piece

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3.2 Technical information

Channel

Dual, isolated between channels

Power supply

9.0 V DC -1 *6LR61 battery Adapter output:9.0Vdc, 800mA

Operating conditions

5°C to 40°C( 41 to 104 with a relative humidity of 30%-75%, atmospheric pressure from 700 to 1060 Hpa

℉ ℉)

Storage conditions

-10°C to 50°C （14 to 122 with a relative humidity of 10%-90%,atmospheric pressurefrom 700 to 1060 Hpa

℉ ℉)

Dimensions

4.5×2.55×0.9 inches(L*W*H)

Weight

0.28 lbs(With battery)

Tolerance

There may be a ±5% tolerance of all setting and ±10% tolerance of output of intensity.

Timer

Adjustable, from 1 to 60 minutes or continuous, Adjustable in 1minutes each step. Treatment time countdown automatically.

Waveform

Mono-phase square pulse wave

Pulse amplitude

Adjustable, 0~100mA peak at 1000 ohm Load each channel, 1mA/Step.

Pulse Width

Adjustable, from 50 to 300us

microseconds, 10μS/step

Pulse Rate

Adjustable, from 1 to 150 Hz, 1 Hz/step

Technical specifications for Transcutaneous Electrical Nerve Stimulator (TENS) mode

Burst (P1)

Burst rate: Adjustable, 0.5 ~ 5Hz;

0.1Hz/step Pulse width adjustable, 50~300μS Frequency fixed = 100 Hz

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Technical specifications for Electrical Muscle Stimulation (EMS) mode

Waveform

Mono-phase square pulse wave

Pulse amplitude

Adjustable, 0~100mA peak at 1000 ohm Load each channel, 1mA/Step.

Pulse Width

Adjustable, from 50 to 300μS microseconds, 10μS/step.

Pulse Rate

Adjustable, from 1 to 150 Hz, 1 Hz/step

Contraction time

Adjustable, 1~30 seconds , 1 Sec./ step

Relaxation (OFF)time

Adjustable, 0~60 seconds , 1 Sec./ step

Ramp time

Adjustable, 1~6 seconds, 1 Sec. / step, The “On” time will increase and decrease in the setting value.

Normal (P2)

The pulse rate and pulse width are adjustable. It generates continuous stimulation based on the setting value.

Pulse Width Modulation (P3)

The pulse width is automatically varied in a cycle time. The pulse width is decreased from its original setting to 60% in setting cycle time, and then increased from 60% to its original setting in nest setting cycle time. In this program, pulse rate (1 to 150Hz), pulse width (50 to 300us) and cycle time (5 to 30 sec) are fully adjustable.

Pulse Rate Modulation (P4)

The pulse rate is automatically varied in a cycle time. The pulse rate is decreased from its original setting to 60% in setting cycle time, and then increased from 60% to its original setting in nest setting cycle time. In this program, pulse rate (1 to 150Hz), pulse width(50 to 300us) and cycle time (5 to 30 sec) are fully adjustable.

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Alternate (P2)

The Stimulation of the CH2 will occur after the 1st working of CH1 is completed. In this program, The “ON” time including “Contraction”, “Ramp Up” and “Ramp Down” time. The OFF Time should be equal or more than the ON Time ON TIME=Contraction + Ramp up + Ramp down OFF TIME≥ON TIME

Delay (P3)

The Stimulation of the CH2 will occur after the 1st working of CH1 is started+ Delay Time. Delay time is adjustable form 1 to 10 sec. In this program, The “ON” time including “Contraction”, “Ramp Up” and “Ramp Down” time. ON TIME=Contraction + Ramp up + Ramp down

Technical specifications for Interferential (IF) mode

Waveform

Bi-phase square pulse

Pulse amplitude

Adjustable, 0~70mA peak to peak at 1000 ohm Load each channel, 1mA/Step.

Pulse Rate

Channel 1 – Fundamental frequency: 4000 Hz fixed Channel 2 – Selectable frequency: 4001 to 4150 Hz Interference frequency: 1 to 150 Hz.

Phase Width

125μS

Synchronous (P1)

Stimulation of both channels occurs synchronously. The “ON” time including “Contraction”, “Ramp Up” and “Ramp Down” time.ON TIME=Contraction + Ramp up + Ramp down

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The pulse rate of the CH1 is fixed in 4000Hz; CH2 pulse rate is increased from 4001Hz to 4010Hz in a cycle time, and then decreased from 4010Hz to 4001Hz in nest setting cycle time. In this program, CH2 interference frequency is varied from 1Hz to 10Hz, cycle time (5 to 30 sec) is fully adjustable. CH 2 pulse rate=4000Hz+ Interference frequency

The pulse rate of the CH1 is fixed in 4000Hz; CH2 pulse rate is increased from 4001Hz to 4150Hz in a cycle time, and then decreased from 4150Hz to 4001Hz in nest setting cycle time. In this program, CH2 interference frequency is varied from 1Hz to 150Hz, cycle time (5 to 30 sec) is fully adjustable. CH 2 pulse rate=4000Hz+ Interference frequency

The pulse rate of the CH1 is fixed in 4000Hz; CH2 pulse rate is increased from 4080Hz to 4150Hz in a cycle time, and then decreased from 4150Hz to 4080Hz in nest setting cycle time. In this program, CH2 interference frequency is varied from 80Hz to 150Hz, cycle time (5 to 30 sec) is fully adjustable. CH 2 pulse rate=4000Hz+ Interference frequency

The pulse rate of the CH1 is fixed in 4000Hz; CH2 pulse rate is automatically varied in a cycle time. Interference frequency is increased from its original setting to 60% in setting cycle time, and t hen decreased from 60% to its original setting in nest setting cycle time. In this program, CH2 interference frequency (2 to 150Hz) and cycle time (5 to 30 sec) are fully adjustable. CH 2 pulse rate=4000Hz+ Interferencefrequency

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Constant(P1)

Constant stimulation based on setting value. Only pulse width, pulse rate and timer are adjustable in this program. “Constant” is equal to the “Normal” mode of a TENS therapeutic mode

Pulse Width Modulation (P2)

The pulse width is automatically varied in a cycle time. The pulse width is decreased from its original setting to 60% in setting cycle time, and then increased from 60% to its original setting in nest setting cycle time. In this program, pulse rate (1 to 150Hz), pulse width (2 to 200ms) and cycle time (5 to 30 sec) are fully adjustable.

Pulse Rate Modulation (P3)

The pulse rate is automatically varied in a cycle time. The pulse rate is decreased from its original setting to 60% in setting cycle time, and then increased from 60% to its original setting in nest setting cycle time. In this program, pulse rate (1 to 150Hz), pulse width (2 to 200ms) and cycle time (5 to 30 sec) are fully adjustable.

Technical specifications for Microcurrent (MIC) mode

Waveform

Mono-phase square pulse wave

Pulse amplitude

Adjustable, 0~0.7mA peak at 1000 ohm Load each channel, 0.01mA/Step

Pulse Width (P.W.)

Adjustable, from 2 to 200ms, 1ms/step

Pulse Rate (P.R.)

Adjustable, from 1 to 150 Hz, 1 Hz/step

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CH1

CH2

Pulse Width Modulation

Pulse Rate Modulation

3.3 The waveforms of the stimulation programs

Burst

Normal

Synchronous

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Delay

Interferential

Alternate

CH1

CH2

CH1

CH2

Microcurrent(Constant) (P1)

Microcurrent Pulse Width Modulation P2)(

Microcurrent Pulse Rate Modulation(P3)

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4.1.2 Disposal of battery

Spent batteries do not belong in the household waste. Dispose of the battery according to the current federal, state and local regulations. As a consumer, you are obligated by law to return spent battery.

4. Instruction for use

4 .1 Battery

4.1.1 Check/Replace the battery

Over time, in order to ensure the functional safety of device, changing the battery is necessary.

1) Slide the battery compartment cover and open.

2) Insert the 9V battery into the battery compartment.

3) Make sure you are installing the battery properly. Be sure to match the positive and negative ends of the battery to the marking in the battery compartment of the device.

4) Press and pull down following the direction of the arrow indicated on the photo.

5) Replace the battery compartment cover and press to close.

6) If replace the battery, you should slide the battery compartment cover and open. Pull up the battery following the direction of the arrow indicated on the photo. And insert the 9V battery according to the above step 2) to 5).

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4.2 Connect electrodes to lead wires

Insert the lead wire connector into electrodes connector (standard 0.08 inch female connection). Make sure no bare metal of the pins is exposed.

Caution: Always use the electrodes with the requirements of the IEC/EN60601-1 ， ISO10993-1/-5/-10 and IEC/ EN60601-1-2, such as with CE mark, or which are legally marketed in the US under 510(K) procedure.

Caution:

1) Battery may be fatal if swallowed. Therefore, keep the battery and the product out of the range of children, if a battery was swallowed, consult a physician immediately.

2) If a battery has leaked, avoid contact with skin, eyes and mucus membranes, Rinse the affected spots with lots of clear water immediately and contact a physician right away.

3) Battery may not be charged, dismantled, thrown into fire or short-circuited.

4) Protect battery from excess heat; Take the battery out of the product if they are spent or in case you no longer use the article. This prevents damage caused by leaking battery.

5) Always replace the same type battery.

4.3 Connect lead wires to device

1) Before proceeding to this step, be sure the device is completely turns OFF.

2) The wires provided with the system insert into the jack sockets located on top of the device.

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4.4 Electrode

4.4.1 Electrode options

The electrodes are disposable and should be routinely replaced when they start to lose their adhesive nature. If you are unsure of your electrode adhesive properties, order replacement electrodes. Replacement electrodes should be re-ordered through or on the advice of your physician to ensure proper quality. Follow application procedures outlined in electrode packing, to maintain optimal stimulation and to prevent skin irritation.

4.4.2 Place electrodes on skin

3) Holding the insulated portion of the connector, push the plug end of the wire into one of the jacks (see drawing); one or two sets of wires may be used.

4) This device has two output receptacles controlled by Channel 1 and Channel 2 at the top of the unit. You may choose to use one channel with one pair of lead wires or both channels with two pairs of lead wires. Using both channels gives the user the advantage of stimulating two different areas at the same time.

Caution: Do not insert the plug of the patient lead wire into any AC power supply socket.

Apply electrodes to the exact site indicated by your physi cian or t h e r a p i s t , b e f o r e a p p l y i n g electrodes, be sure the skin surface over which electrodes are placed is thorou g h l y c l e a n ed a n d d r i e d .

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4.4.3 Electrode placement

The placement of electrodes can be one of the most important parameters in achieving success with therapy. Of utmost importance is the willingness of the physician to try the various styles of electrode placement to find which method best fits the needs of the individual patient. Every patient responds to electrical stimulation differently and their needs may vary from the conventional settings suggested here. If the initial results are not positive, speak to your physician ab o ut al t e rna t i ve st i mula t ion s e t tin g s a n d/or e le ct r o d e p la c e m e n t s . O nc e a n a cc ep t a b l e placement has been achieved, mark down the electrodes sites and the settings, so the patient can easily continue treatment at home.

Make sure the electrodes are placed firmly to the skin and make good contact between the skin and the electrodes. Place the electrodes over the skin; attach them properly, firmly, and evenly.

Caution:

1) Before applying the self-adhesive electrodes, it is recommended to wash and degrease the skin, and then dry it.

2) Do not turns on the device when the self adhesive electrodes are not positioned on the body.

3) Never remove the self-adhesive electrodes from the skin while the device is still turns on.

4) It is recommended that, at minimum, 4cm*4cm self-adhering based, square electrodes are used at the treatment area.

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4.6 Select the Therapeutic Mode

There are 4 therapeutic modes available –TENS, IF, MIC and EMS. The therapeutic mode can be selected by pressing the [M] control.

Caution: Consult your physician for your suitable therapeutic mode

4.5 Turn on

Before using the device for the first time, you are strongly advised to take careful note of the cou nter- indicatio ns an d safety measures detailed at the beginning of this manual (Safety information), as this powerful equipment is neither a toy nor a gadget!

In order to turn on the device, keep the [ ] button pressed down until the operation page appears on the screen.

4.7 Steps to Set a New Program

4.7.1 TENS Setting

Press the [S] button cycle to enter the setting state. The settings can be adjusted according to the following steps:

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3) Set Timer

Press [S] button cycle to enter this setting. The treatment time is adjustable from 1 to 60 minutes or Continue. Press [▲ ] or [▼ ] button control to adjust setting. You can set the timer to “Continuous” mode by pressing the [▲] control when it shows 60 minutes. Its output will be shut off when time is up.

4) Set Pulse Width

5) Set Pulse Rate

Pulse Width is adjustable from 50 uS to 300 uS. Press [S] button to enter this menu, then press [▲ ] or [▼ ] button to adjust the setting.

Pulse rate is adjustable from 1 Hz to 150 Hz (0, 5 Hz to 5 Hz for Burst). Press [S] button cycle to enter this menu, and then press [▲] or [▼] button to adjust the setting.

1) Set the Therapeutic Program

2) Set Cycle Time (Optional)

There are 4 programs in TENS therapeutic mode available – Burst (P1), Normal (P2), Pulse Width Modulation ( P 3), and Pulse Rate Modulation (P4). The ther a peutic progr a m can be

selected by pressing the [▲] and [▼ ] button. When you choose to [B] program, program [B] outside of the box will be flashing.

Cycle time is adjustable form 5 to 30 seconds. Only modulation has this parameter setting. Press [S] button cycle to enter this menu, and then press the [▲] and[▼] button to adjusting the setting.

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2) Set Timer

Press [S] button cycle to enter this setting. The treatment time is adjustable from 1 to 60 minutes or Continue. Press [▲ ] or [▼] control to adjust setting. You can set the timer to “Continuous” mode by pressing the [▲] button when it shows 60 minutes. Its output will be shut off when time is up.

Channel 1 has 4000 Hz fixed Fundamental frequency. Channel has selectable frequency from 4001 to 4150 Hz; Interference frequency is adjustable form 2 Hz to 150 Hz. Only [P4] has this parameter setting. Press [S] button cycle to enter this menu, and then press the [▲] and [▼] button to adjusting the setting.

4.7.2 IF Setting

Press the [S] button to enter the setting state. The settings can be adjusted according to the following steps:

1) Set the Therapeutic Program

There are 4 programs in IF therapeutic mode available. The therap e u t i c program can be selected by pressing the [▲] and [▼ ] bu t t o n . T h e m o d e y o u selected will show up on the top of liquid crystal display.

3) Set Interference frequency (optional)

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The therapeutic program can be selected by pressing the [▲ ] and [▼ ] button. The mode you selected will show up on the top of liquid crystal display.

Press [S] button cycle to enter this setting. The treatment time is adjustable from 1 to 60 minutes or Continue. Press [▲ or [▼ button control to adjust setting. You can set the timer to “Continuous” mode by pressing the[▲] control when it shows 60 minutes. Its output will be shut off when time is up.

] ]

2) Set Timer

3)Set Pulse Width

Pulse Width is adjustable from 2ms to200ms. Press [S] button cycle to enter this menu, then press [▲] or [▼] button to adjust the setting.

Cycle time is adjustable form 5 to 30 seconds. Press [S] button cycle to enter this menu, and then press the [▲ and [▼ button to adjusting the setting.

] ]

4) Set Cycle Timer

4.7.3 MICROCURRENT Setting

Press the [S] button cycle to enter the setting state. The settings can be adjusted according to the following steps:

1) Set the Therapeutic Program

There are 3 programs in MIC therapeutic program available – Co n sta n t ( P 1), P u lse W i dth Modulation (P2), and Pulse Rate Modulation (P3).

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4.7.4 EMS Setting

Press the [S] button cycle to enter the setting state. The settings can be adjusted according to the following steps:

1) Set the Therapeutic Program

There are 3 programs in EMS t h er ap e ut ic m od e a v ai l a b le –Delay (P1), Synchronous (P2) a n d A l t e r n a t e ( P 3 ) . T h e therapeutic program can be selected by pressing the [▲ and]

[▼ ] button. When you choose to [S] program, program [S] outside of the box will be flashing.

Pulse rate is adjustable from 1 Hz to 150 Hz. Press [S] button cycle to enter this menu, and then press [▲] or [▼] button to adjust the setting.

4) Set Pulse Rate

5) Set Cycle Time (Optional)

Cycle time is adjustable form 5 to 30 seconds. Only modulation m o d e h a s t h i s p a r a m e t e r setting. Press [S] button cycle to enter this menu, and then press the [▲ and [▼ button to adjusting the setting.

] ]

2) Set Timer

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5) Set Delay Time(Optional)

Delay time is adjustable form 1 to 10 seconds. Only Delay therapeutic program ha s this parameter setting. Press [S] button cycle to enter this menu, and then press the [▲ ] and [▼ ]button to adjusting the setting.

The ramp time controls the time of output current that increase from 0 to the setting level, and from the setting value to 0. When the ramp time is set, each contraction may be ramped up and down in order that the signals come on and come off gradually and smoothly. The ramp time is adjustable from 1 to 6 seconds.

6) Set Ramp Time

pressing the [▲ ] button when it shows 60 minutes. Its output will be shut off when time is up.

3) Set Pulse Width

The pulse width determines the length of time. Each electrical signal is applied through the skin, which c o nt ro l s t h e s tr e ng th a nd s en sa t io n o f th e stimulation. Press [S] button cycle to enter this setting. The pulse width is adjustable from 50 to 300 uS.Press [▲] or [▼] button to adjust the setting.

The pulse rate determines how many electrical impulses are applied through the skin each second. Press [S] button cycle to enter this menu. By

the [▲ ] or [▼ ] button to adjusting the setting. The pulse rate is adjustable from 1 Hz to 150 Hz.

4) Set Pulse Rate

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8) Set Relaxation (OFF) time

The Off Time controls the time of relaxation. The relaxation time can be adjusted. Press [S] button cycle to enter this menu, and then press the [▲] and [▼ ] button to adjusting the setting. Both channels' stimulation is cycled on and off by the contraction and relaxation settings. The range is adjustable from 0 to 60 seconds.In Alternate program, the OFF Time should be equal or more than the ON Time. (OFF TIME ≥ON TIME)

Press the intensity control button ([▲ ] and [▼ ] ) to control the intensity output. Slowly press the intensity b u t t on c on t r o l u n ti l y o u r e a c h t h e s e t t i n g recommended by your physician or therapist. Repeat for the other channel, if both channels are to be used.

4.8 Adjust Channel Intensity

The contract Time controls the t i me o f st im u la t io n. Th e c o n t r a c t i o n t i m e c a n b e adjusted. Press [S] button cycle to enter this menu, and then press the [▲ ] and [▼ ] button to adjusting the setting.

Both channels’ stimulation is cycled on and off by the contraction and relaxation settings. The range is adjustable from 1 to 30 seconds.

7) Set Contract Time

Caution: Contract time has not including the ramp up and ramp down time, ON time=Ramp up + Contract time + Ramp down.

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4.9. Lock the button

The Safety Lock Feature automatically activates after there is no operation in the panel for 30 seconds by locking out the ability to press the buttons. This is a safety feature to prevent accidental changes to your settings and to prevent accidental increases to the intensity levels. You can press either one of the [▼ ] buttons to unlock the device.

4.10. Stop the treatment

When you have activated the treatment timer, you can press the [M] button or the [ ▼ ] button to control stop

the treatment.

Caution: Default state, if the button is locked, you can

press only one of the [ ▼ ]buttons to unlock, and then press the [M] button or the [▼ ] button to control stop the treatment.

4.11. Turn OFF

Press [ ] button and hold for approx.3 seconds to Turn OFF the device.

If the stimulation levels are uncomfortable or become uncomfortable, reduce the stimulation intensity to a comfortable level and contact your medical practitioner if problems persist.

TENS, EMS and IF therapeutic mode. If the electrodes no placed firmly on skin or the device has not connected on the electrodes, the stimulator's output intensity surpasses 12mA, the intensity will enulls automatically.

Caution:

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4.12. Low battery indicator

When the low power indicator flashes, the device will

be turns off automatically, the battery should be

replaced with a new one as soon as possible.

However, the unit may continue to operate for a few

more hours depends on the setting intensity level.

Caution:

If there is no operation in the panel for 3 minutes in the waiting state, the device will be turns off automatically.

In shutdown state, keep pressing the channel 2

[ ▼ first, and then press [ ]button at the same

to restore factory parameter settings

]

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5. Program

Mode Program

Modulation

Method

Frequency

Pulse

Width

Treat time

TENS

Burst

0.5-5Hz

50-300us

1-60min,continous

Continuous

1-150Hz

50-300us

1-60min,continous

Pulse width

modulation

1-150Hz

50-300us 1-60min,continous

Frequency

modulation

1-150Hz

50-300us 1-60min,continous

EMS

Synchronous

1-150Hz

50-300us 1-60min,continous

Asynchronous

1-150Hz

50-300us 1-60min,continous

Delay

1-150Hz

50-300us 1-60min,continous

Frequency

modulation

4kHz

4001-4010Hz

125us 1-60min,continous

Frequency

modulation

4kHz

4001-4150Hz

125us 1-60min,continous

Frequency

modulation

4kHz

4080-4150Hz

125us 1-60min,continous

Frequency

modulation

4kHz

4001-4150Hz

125us 1-60min,continous

MIC

Continuous

1-150Hz

2-200ms 1-60min,continous

Pulse width

modulation

1-150Hz

2-200ms

1-60min,continous

Frequency

modulation

1-150Hz 2-200ms 1-60min,continous

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6. Cleaning and Care

6.1 Tips for skin care

To avoid skin irritation, especially if you have sensitive skin, follow these suggestions:

1) Wash the area of skin where you will be placing the electrodes, using mild soap and water before applying electrodes, and after taking them off. Be sure to rinse soap off thoroughly and dry skin well.

2) Excess hair may be clipped with scissors; do not shave stimulation area.

3) Wipe the area with the skin preparation your clinician has recommended. Let this dry. Apply electrodes as directed.

4) Many skin problems arise from the “pulling stress” from adhesive patches that are excessively stretched across the skin during application. To prevent this, apply electrodes from centre outward; avoid stretching over the skin.

5) To minimize “pulling stress”, tape extra lengths of lead wires to the skin in a loop to prevent tugging on electrodes.

6) When removing electrodes, always remove by pulling in the direction of hair growth.

7) It may be helpful to rub skin lotion on electrode placement area when not wearing electrodes.

8) Never apply electrodes over irritated or broken skin.

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6.2 Cleaning the device

1) Remove the battery from the device every time when you clean.

2) Clean the device after use with a soft, slight moistened cloth. In case of more extreme soiling you can also moisten the cloth with mild soapy water.

3) Do not use any chemical cleaners or abrasive agents for cleaning.

6.3 electrodes

1) Use the device only with the leads and electrodes provided by the manufacturer. Use only the electrode placements and stimulation settings prescribed by your physician or therapist.

2) It is recommended that, at minimum, 4cm*4cm self

-adhering based, square electrodes are used at the treatment area.

3) Inspect your electrodes before every use. Replace electrodes as needed. Reusable electrodes may cause slight skin irritation, lose adhesion and deliver less stimulation if overused.

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To use these electrodes:

1) Attach the electrode to the lead wire.

2) Remove the protective backing from the electrode surface. Do not throw away the protective backing because it is reused after the treatment session has been completed.

3) Place the tacky surface to the prescribed skin area by pressing the electrode firmly against the skin.

To remove your electrodes:

1) Lift the corner of the electrode and gently remove it from the skin.

2) Apply the protective backing to the tacky side of the electrode. Place the electrode on the side of the protective backing that is labeled with the word on.

3) It may be helpful to improve repeated application by spreading a few drops of cold water over the adhesive and turn the surface up to air dry. Over Saturation with water will reduce the adhesive properties.

4) Between uses, store the electrodes in the resealable bag in a cool dry place.

Caution: Do not pull on the electrode wire. Doing so may damage the wire and electrode. Do not apply to broken skin. The electrodes should be discarded when they are no longer adhering. The electrodes are intended for single patient use only. If irritation occurs, discontinue use and consult your clinician. Read the instructions for use of self-adhesive electrodes before application.

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Always use the electrodes with the requirements of the IEC/EN60601-1, ISO10993-1/-5/-10 and I EC/ EN60601-1-2, such as with CE mark, or are legally marketed in the US under 510(K) procedure.

6.4 Cleaning the Electrodes cords

Clean the electrode cords by wiping them with damp cloth. Coating them lightly with talcum powder will reduce tangles and prolong the life.

6.5 Maintenance

1) Maintenance and all repairs should only be carried out by an authorized agency. The manufacturer will not be held responsible for the results of maintenance or repairs by unauthorized persons.

2) The user must not attempt any repairs to the device or any of its accessories. Please contact the retailer for repair.

3) Opening of the equipment by unauthorized agencies is not allowed and will terminate any claim to warranty.

4) Check the unit before each use for signs of wear and/or damage. Replace wear items as required.

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7. Troubleshooting

If your device does not seem to be operating correctly, refer to the chart below to determine what may be wrong. Should none of these measures correct the problem, the device should be serviced.

Problem

Possible Cause Solution

Displays fail to light up

Battery contact failure

1. Try fresh batteries.

2. Ensure batteries are inserted correctly. Check the following contacts: All contacts are in place. All contacts are not broken.

Stimulation weak

Electrodes

1. Dried out or contaminated

2. Placement Lead wires

1.Old/worn/ damaged

Replace and re-connect

Replace

Stimulation is

uncomfortable.

Intensity is too high Electrodes are too close together Damaged or worn electrodes or lead wires Electrode active area size is too small.

Decrease intensity. Reposition the electrodes.

Replace.

Replace electrodes with ones that have an active area no less than 16.0cm 2(4cm*4cm).

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Intermittent output

Lead wires

Program option in use

1. Verify connection is secure. Insure firmly.

2. Turn down the intensity. Rotate lead wires in socket 90°. If still intermittent, replace lead wire.

3. If still intermittent after replacing lead wire, a component may have failed. Call the repair department.

Some programs will seem intermittent. This is expected. Refer to the Program Option Controls in the Operation section for a description of the program option.

Stimulation is ineffective.

Improper electrode and applicator placement Unknown

Reposition electrode and applicator Contact clinician.

8. Storage

1) For a prolonged pause in treatment, store the

device in a dry room and protect it against heat,

sunshine and moisture.

2) Store the device in a cool, well-ventilated place

3) Never place any heavy objects on the device.

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9. Disposal

Used fully discharged batteries must be disposed of in a specially labeled collection container, at toxic waste collection points or through an electrical retailer. You are under legal obligation to dispose of batteries correctly.

Please dispose of the device in accordance with the legal obligation.

10. Electromagnetic Compatibility (EMC) Tables

Guidance and manufacturer's declaration

- electromagnetic emissions

The device is intended for use in the electromagnetic environment specified below. The customer or the user assures that it is used in such an environment.

Emissions test

Compliance

Electromagnetic environment

- guidance

RF emissions CISPR 11

Group 1

The device uses RF energy only for its internal function. Therefore, its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment.

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RF emissions CISPR11

Class B

Harmonic emissions lEC 61000-3-2

Not applicable

Voltage fluctuations /flicker emissions lEC 61000-3-3

Not applicable

The device is suitable for use in all establishments other than domestic and those directly connected to the public lowvoltage power supply network that supplies buildings used for domestic purposes.

Guidance and manufacturer's declaration —

electromagnetic immunity

The device is intended for use in the electromagnetic environment specified below. The customer or the user should assure that it is used in such an environment.

Immunity test

IEC 60601 test level

Electrostatic discharge (ESD) EC 61000-4-2

± contact

±8 kV air

6 kV

Compliance level

Electromagnetic environment guidance

± contact

±8 kV air

6 kV

Floors should be wood, concrete or ceramic tile. If floors are covered with synthetic material, therelative humidity should be at least 30 %.

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Guidance and- manufacturer's declaration.

Electromagnetic immunity

The device is intended for use in. the electromagnetic environment specified below. The customer or the user should assure that it is used in such an environment.

Emissions test

IEC 60501 test level

Compliance level

Conducted

RF lEC

61000-4-6

Radiated

RF lEC

61000-4-3

3 Vrms

150 kHz

to 80 MHz

3 V/m80

MHz to

2.5 GHz

3 Vrms

3 V/m

Portable and mobile RF communications equipment should be used no closer to any part of the device, including cables, than the recommended separation distance calculatedfrom the equation applicable to the frequency of the transmitter. Recommended separation distance

Electromagnetic environment guidance

, 80MHz to 800MHz

, 800MHz to 2,5MHz

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Where P is the maximum output power rating of the transmitter In watts (W) according to the. Transmitter manufacturer and d Is the recommended separation distance in meters (m).

Field strengths from fixed RF transmitters, as determined by an electromagnetic site survey, should be less than the compliance level in each frequency range. Interference may occur In the vicinity of equipment marked with the following symbol:

NOTE I At 80 MHz ends 800 MHz. the higher frequency range applies. NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.

1. Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted

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theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the device is used exceeds the applicable RF compliance level above, should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the device.

2.Over the frequency range 150 kHz to 80 MHz, field

strengths should be less than [Vi] V/m.

Rated

maximum

output

power of

transmitter

Separation distance according to frequency of transmitter

150 kHz to 80 MHz

Recommended separation distances between

portable and mobile RF communications equipment

and the device

The device is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the device can he l p p r ev e nt e l e ct r om a gn e ti c i n te r fe r en c e b y maintaining a minimum distance between portable a n d m o b i l e R F c o m m u n i c a t i o n s e q u i p m e n t (t ransmit te rs) an d th e a s r ecommen ded be low, according to the maximum output power of the communications equipment.

d=2.3

80 MHz to 800 MHz

800 MHz to 2,5 GHz

0.01 0.12 0.12

0.23

0.1

0.38 0.38 0.73

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1 1.2 1.2

2.3

3.8 3.8 7.3

100

12 12

For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) accordable to the transmitter manufacturer. NOTE I At 80 MHz and 800 MHz. the separation distance for the higher frequency range applies. NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.

11. Glossary of Symbols

Batch code

Electrical devices are recyclable material and should not be disposed of with household waste after their useful life! Help us to protect the environment and save resources and take this device to the appropriate collection points. Please contact the organization which is responsible for waste disposal in your area if you have any questions.

Serial number

Attention: Read the operating instruction for use!

Degree of Electrical Protection BF

Complies with MDD 93/42/EEC and amended by directive 2007/47/EC requirements, Notified body TUV SUD (0123)

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12. Warranty

Please contact your dealer or the device centre in case of a claim under the warranty. If you have to send in the unit, enclose a copy of your receipt and state what the defect is.

The following warranty terms apply:

1) The warranty period for device is one years from date of purchase. In case of a warranty claim, the date of purchase has to be proven by means of the sales receipt or invoice.

2) Repairs under warranty do not extend the warranty period either for the device or for the replacement parts.

3) The following is excluded under the warranty: All damage which has arisen due to improper treatment, e.g. nonobservance of the user instruction. All damage which is due to repairs or tampering by the customer or unauthorized third parities.

Damage which has arisen during transport from the manufacturer to the consumer or during transport to the service centre. Accessories which are subject to normal wear and tear.

4) Liability for direct or indirect consequential losses caused by the unit is excluded even if the damage to the unit is accepted as a warranty claim.

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Allied Health Medical Supplies. 152A Gaffney St Coburg VIC 3058 Australia

Made in China

PRODUCT CODE: MT8000

Tel: 03 9366 6611

www.physipod.com.au

Manufactured For: