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1

Safety

Warning and

Cautions

1.

Do not use this device if you have a cardiac pacemaker, implanted defibrillator, or other implanted 
metallic or electronic device. Such use could cause electric shock, burns, electrical interference, or 
death.

2.

If you are in the care of a physician, consult with your physician before using this device; 

3.

Do not apply 

stimulation on your heart, head, mouth, pudendum or blemished skin areas;

4.

Do not apply stimulation across your chest because the introduction of electrical current into the 
chest may cause rhythm disturbances to your heart, which could be lethal; 

5.

Do not apply during pregnancy.

6.

Do not apply stimulation over painful areas. If you have painful areas, you should consult with your 
physician before using this device; 

7.

Do not apply stimulation over open wounds or rashes, or over swollen, red, infected, or inflamed 
areas or skin eruptions (e.g., phlebitis, thrombophlebitis, varicose veins); 

8.

Do not apply stimulation over, or in proximity to, cancerous lesions; 

9.

Do not apply stimulation in the presence of electronic monitoring equipment (e.g., cardiac monitors, 

ECG alarms), which may not operate properly when the electrical stimulation device is in use; 

10. Do not apply stimulation when in the bath or shower; 

11. Do not apply stimulation while sleeping; 

12. Do not apply stimulation while driving, operating machinery, or during any activity in which 

electrical stimulation can put you at risk of injury;

13.

Do not use the device on children;

14. Consult with your physician before using this device, because the device may cause lethal rhythm 

disturbances to the heart in susceptible individuals; and 

15.

Apply stimulation only to normal, intact, clean, healthy skin;

16.

Do not use this device in high humidity areas such as a bathroom;

17. Do not attempt to move the electrode heads while the device is operating; and

18. Keep the device away from wet, high temperature and di

rect sunshine. Shady and dry place is good 

for device stock.

1.

This device is not effective for pain of central origin, including headache; 

2.

This device  is not a substitute for pain medications and other pain management therapies; 

3.

This device has no curative value; 

4.

This device  is a symptomatic treatment and, as such, suppresses the sensation of pain that would 

otherwise serve as a protective mechanism; 

5.

The long

-term effects of electrical stimulation are unknown; 

6.

Since the effects of stimulation of the brain are unknown, stimulation should not be applied across 

your head, and electrodes should not be placed on opposite sides of your head; 

Summary of Contents for PL009

Page 1: ...device is in use 10 Do not apply stimulation when in the bath or shower 11 Do not apply stimulation while sleeping 12 Do not apply stimulation while driving operating machinery or during any activity in which electrical stimulation can put you at risk of injury 13 Do not use the device on children 14 Consult with your physician before using this device because the device may cause lethal rhythm di...

Page 2: ...kin that lack normal sensation 15 Keep this device out of the reach of children 16 Turn off the stimulator if the stimulation feels unpleasant or does not provide pain relief 17 Use this device only with the leads electrodes and accessories recommended by the manufacturer Adverse Reactions You may experience skin irritation and burns beneath the stimulation electrodes applied to your skin You may ...

Page 3: ...ks The operational principle of the device is to generate small pulses of electrical current and deliver the pulses to an ordinary user s skin through electrode adhesive pads such that the underlying nerves are activated and the pain associated with sore and aching muscles is temporarily relieved ...

Page 4: ...artment and direction Make sure both the power knobs on both sides are turned OFF To insert the battery slide the compartment cover downward until the cover pops off Insert 4pc AAA batteries according to the diagram in the battery compartment and then close the cover Match the flat end of the battery to the negative mark and match the other end to the positive mark 2nd Step Connect the electrode p...

Page 5: ...t This knob is also for the Intensity control 5th Step Select one of automatic stimulation programs 5 automatic stimulation programs repeat Five automatic stimulation programs for waist shoulder joint hand foot sole plus a repeat to stimulate the same area again The LCD display will show a timer of 15 minutes when you choose one of them 6th Step Gradually increase the massage intensity to a comfor...

Page 6: ...on both sides to turn off the device The best treatment time is 15 minutes each session Disconnect the wires and electrode pads after the massaging Take the batteries out if not used frequently Put the device in a dry and shady place Please make sure every part of device and accessories in good conditions before the use of the device Ask for replacement in case of any breaking cracking and scratch...

Page 7: ...Output Voltage 12 8V 500 51V 2 k 368V 10 k Maximum Output Current 15mA 500 3 2mA 2 k 0 6mA 10 k Duration of primary depolarizing phase 40 msec Pulse Duration 100 680 µsec Frequency 1 100Hz Net Charge 18000µC 500 Maximum Phase Charge 23 µC 500 Maximum Current Density 1 4mA cm 500 Maximum Average Current 18mA 500 Maximum Average Power Density 0 23W cm 500 Burst Mode Pulses per burst 1 Bursts per sec...

Page 8: ...n a button of Massage Beat or Knead is selected the LCD screen displays an icon corresponding to the selected button 3 When a button of Waist Shoulder Joint Hand Foot or Sole is selected the LCD screen displays a dot on a position in a human figure icon corresponding to the selected button When the speed adjustment key is pressed the LCD screen displays a speed bar comprising of squares which are ...

Page 9: ...eracorp com for additional Product information Electronic Pulse Massager Part PL009 Electrode Pads Part PL009 P Electric Wire Part PL009 W 1 The PL009 Electronic Pulse Massager is compliance with Medical electrical equipment Part 1 General requirements for safety Medical electrical equipment Part 1 2 General requirements for safety Collateral Standard Electromagnetic compatibility Requirements and...

Page 10: ...onnected to the electrode heads and the main device properly Are the batteries dead Remove clean and place back on the skin If so then separate Disconnect clean and reconnect all the parts Replace the dead batteries Skin turns red Is treatment time too long Treat another area Skin feels numb Are electrode heads dirty Do the electrode heads touch the skin closely Clean with damp cloth Remove and pl...

Page 11: ... and dated proof of purchase sales receipt when contacting Prospera for the warranty service Non warranty service is provided on a per incident basis The consumer will verify that the product has failed and provide information for servicing the unit All applicable repairs parts shipping handling local tax and per incident fees will be charged for non warranty repairs and support calls ...

Page 12: ...12 Positions W a is t S h o u ld e r J o in ts Sole of Foot v Hand or Foot n ...

Page 13: ...odel Date of Purchase First Name Address Purchase Price Retailer Last Name City Phone Signature and date State Email Zip Please mail to Prospera Corporation 405 Boulder Ct Ste 500 Pleasanton CA 94566 Telephone 925 225 0888 Fax 925 225 0660 Email sales prosperacorp com ...

Page 14: ...Manufacturer s Contact Information Prospera Corporation U S 405 Boulder Court Suite 500 Pleasanton CA 94566 Tel 925 225 0888 Fax 925 225 0660 Email jane prosperacorp com ...

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