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Stimplus and Stimplus Pro Instructions for use
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1. Stimplus and Stimplus Pro Instructions for use Caution Federal Law restricts this device to sale or use by or on the order of a practitioner so licensed by the State STIMPLUS pe STIMPLUS Contents Introduction to Patient and Professional 2 Unique Features 3 How to Use the Body Clock Stimplus 3 Controls and Indicators 6 Technical Dad 7 How to Use the Body Clock S mplus Pro 8 Controls and Indicators 11 Technical Dita idos 12 Contraindications 13 A 13 PRECAUTIONS aia 14 Adverse 14 Skin Preparation 14 Electrode Placement Gold Tip 15 Maintenance and Care 15 Checking System Performance and Trouble Shooting 15 Battery Replacement 16 Device Failures 16 Introduction to Patient and Professional The Body Clock Stimplus and Stimplus Pro units are designed for the treatment of symptomatic relief and management of chronic intractable pain and or as an adjunctive treatment in the management of post surgical and post traumatic acute pain The instructions in this manual are designed to cover most oper
2. ational issues However if you have any questions about your particular condition or if problems arise please seek advice from your physician or therapist Unique Features Audio and visual LED intensity indicator 6 intensity levels indicated by 6 LED s 3 choices of stimulation rhythm Timer to adjust treatment duration Stimulates through micro current therapy Ear phone jack to stimulate in silence Free precision extension tip with the Stimplus Pro only Ergonomic design Compact light and user friendly How to Use the Body Clock Stimplus 1 Activate the Body Clock Stimplus by turning the power switch on 2 PLEASE NOTE that the device must be held by the person being treated as the passive contact plate acts as one end of a circuit the other being the tip of the device which is applied to the desired point When treating another party the operator should hold the device onto the points to be treated and ensure that physical contact is maintained between the operator and the other party in order to complete a circuit below Alternatively a wrist strap which is not included with this unit and may be purchased separately may be used to the same effect The wrist strap consists of a lead with the wrist strap at one end and a jack plug at the other end If the strap is used the jack plug should be inserted into the jack on the underside of the device The wrist strap should then be w
3. by 2 Lithium 3 volt batteries amended Weight grams 43 5g Dimensions 16 5cm x 3 7cm x 1 3cm 6 1 2 x 17 16 x 9 16 Classification This unit is fully compliant with EEC Directive 93 42 EEC and is classified as internally powered equipment Type BF It is intended for continuous operation Explanation of Symbols BF Isolated applied part Warning refer to accompanying documents i e this user manual Storage Temperature Range 5 C 65 C Storage Relative Humidity Up to 80 The radio shielding of the device has been ascertained according to VFG 243 1991 interference suppression of ISM devices Max 12V 20 Shapes of output curves under a 500 ohm load How to Use the Body Clock Stimplus Pro 1 Activate the Body Clock Stimplus Pro by turning the power switch on 2 PLEASE NOTE that the device must be held by the person being treated as the passive contact plate acts as one end of a circuit the other being the tip of the device which is applied to the desired point When treating another party the operator should hold the device onto the points to be treated and ensure that physical contact is maintained between the operator and the other party in order to complete a circuit See right Alternatively the wrist strap included with this unit may be used to the same effect The wrist strap consists of a lead with the wrist strap at one end and a jack plug at the other end If the strap is used
4. dromes are undiagnosed until etiology is established Warnings 1 The safety of TENS devices for use during pregnancy or birth has not been established TENS is not effective for pain of central origin 3 TENS devices should be used only under the continued supervision of a physician 4 TENS devices have no curative value TENS is a symptomatic treatment and as such suppresses the sensation of pain which would otherwise serve as a protective mechanism 6 The user must keep this device out of the reach of children 7 Electronic monitoring equipment such as ECG monitors and ECG alarms may not operate properly when TENS stimulation is in use Ui Precautions 1 Isolated cases of skin irritation may occur at the site of electrode gold tip placement following long term application 2 Effectiveness is highly dependent upon patient selection by a person qualified in the management of pain patients Adverse Reactions Skin Irritation and contact burns can occur if the device is used in a constant and continuing stimulation pattern Therefore be very careful as to the condition of the skin beneath the main contact point Skin Preparation Prepare the skin before using the Body Clock Stimplus or Stimplus Pro by thoroughly washing the skin with a mild soap and water solution where contact will be made This will remove non conducting skin oils Then rinse the area with warm water and
5. dry thoroughly Electrode Placement Gold tip e Do not place the device close to any source of excess heat For reducing the pain place the gold tip e Do not operate the device in the on or above the point of pain presence of flammable gases e Do not attempt to open the Body Maintenance and Care Clock Stimplus or Stimplus Pro unit e Do not use battery or power sources Guidelines for optimum performance other than those specified e Do not drop this unit onto a hard e Change the battery regularly surface e The unit must be switched off when changing the battery e The unit should be wiped clean Checking system performance and periodically using a very slightly trouble shooting dampened cloth A mild soap may be used but DO NOT apply solvents e fthe red LED lamp illuminates when the power switch is turned on General Precautions turn the device off Then replace the two three 3 volt batteries and turn e Do not immerse your Body Clock the device on again Ifit still does Stimplus or Stimplus Pro in water or not function return the device for any other liquid repair e f your unit does not appear to be operating properly first change the battery Replacing the battery can eliminate most operational problems Ifthe device still does not appear to function properly return the device for repair e fthe green LED lamp does not illuminate when the stimulation switch is pressed return the device for repair Ba
6. e intensity control switch you can adjust the intensity to a comfortable level pressing the keys to either increase or decrease intensity The intensity level will be indicated by the LED scale If the LED nearest to the tip is flashing the unit is set at minimum intensity If the LED furthest from the tip is flashing the unit is set at maximum intensity or Once stimulation is over the device switches back to search mode and the beeper sound will be audible again During stimulation you may feel the electric current at the stimulation site 11 The ear piece included with this unit may be used to mute the beeper sound enabling the user solely to hear this sound This piece consists of a lead with a jack plug at one end and the ear piece atthe other end To activate the ear piece insert the jack plug into the earphone jack The ear piece is now ready for use 12 A precision extension tip is also provided which can extend the tip to assist you where an acupoint is difficult to reach This is simply placed over the tip and is then ready for use Stimplus Pro Controls and indicators STIM INDICATOR STIM SWITCH TIP GOLD PLATE ACUPOINT 2 5mm PROXIMITY AND EARPHONE INTENSITY JACK INDICATOR LOW BATTERY INDICATOR INTENSITY RHYTHM POWER SWITCH SWITCH SWITCH BATTERY TIME SELECTOR COMPARTMENT PASSIVE NH CONTACT PLATE PASSIVE ELECTRODE JACK RETURN PATH Stimpl
7. e or decrease intensity The intensity level will be indicated by the LED scale Ifthe LED nearest to the tip is flashing the unit is set at minimum intensity Ifthe LED furthest from the tip is flashing the unit is set at maximum intensity 9 10 11 Once stimulation is over the device switches back to search mode and the beeper sound will be audible again During stimulation you may feel the electric current at the stimulation site The ear piece included with this unit may be used to mute the beeper sound enabling the user solely to hear this sound This piece consists of a lead with a jack plug at one end and the ear piece at the other end To activate the ear piece insert the jack plug into the earphone jack The ear piece is now ready for use Stimplus Controls and indicators STIM INDICATOR STIM SWITCH TIP GOLD PLATE ACUPOINT 2 5mm PROXIMITY AND EARPHONE INTENSITY JACK INDICATOR LOW BATTERY INDICATOR INTENSITY RHYTHM POWER SWITCH SWITCH SWITCH BATTERY TIME SELECTOR COMPARTMENT PASSIVE CONTACT PLATE PASSIVE ELECTRODE JACK RETURN PATH Stimplus Technical Data MIN TYP MAX Operating Voltage 4 5V 6 0V 6 5V Output Intensity ohms omA 1 2mA Output Waveform Asymmetrical TIERE rectangular Stimulation Pulse Rate 13 Hz 16 Hz 19Hz Pulse Width 0 15ms Low Battery Indication 4 1V a oV Battery Life 30 sec cycle 3800 cycles Power Source Powered
8. orn by the other party There is then no need for physical contact to be maintained between the operator and the other party Stimulation may then be commenced Begin stimulation by selecting the desired stimulation time by setting the time selector switch A preset time of 30 or 60 seconds may be selected or alternatively manual stimulation which lasts as long as you choose If a preset stimulation time is chosen just press the stimulation button briefly and release The device will automatically stop stimulating when the preset time is over If manual stimulation is selected the device will stimulate for as long as you press the stimulation button When the unit is switched off the intensity level will automatically be reset to minimum You can see the previous intensity setting by pressing the intensity button after which the previous intensity will appear for 5 seconds in the 6 LED bar scale You can then increase or decrease that preset intensity level before beginning stimulation 6 You may select one of three rhythm options during stimulation continuous 1Hz or 4Hz You can select the rhythm that provides the best level of comfort When you begin the stimulation the beeper sound will stop and the green light will flash indicating that stimulation has begun Using the intensity control switch you can adjust the intensity to a comfortable level pressing the or keys to either increas
9. the jack plug should be inserted into the jack on the underside of the device The wrist strap should then be worn by the other party There is then no need for physical contact to be maintained between the operator and the other party Stimulation may then be commenced Begin stimulation by selecting the desired stimulation time by setting the time selector switch A preset time of 15 or 30 seconds may be selected or alternatively manual stimulation which lasts as long as you choose Ifa preset stimulation time is chosen just press the stimulation button briefly and release The device will automatically stop stimulating when the preset time is over If manual stimulation is selected the device will stimulate for as long as you press the stimulation button When the unit is switched off the intensity level will automatically be reset to minimum You can see the previous intensity setting by pressing the intensity button after which the previous intensity will appear for 5 seconds in the 6 LED bar scale You can then increase or decrease that preset intensity level before beginning stimulation 6 You may select one of three frequencies during stimulation 5Hz 10Hz or 20Hz You can select the 1 frequency that provides the best level of comfort When you begin the stimulation the beeper sound will stop and the green light will flash indicating that stimulation has begun Using th
10. ttery Replacement When replacing the batteries ensure that the power switch is turned off Then remove the battery compartment cover and take out the two lithium three 3 volt batteries and replace them with two new two lithium three 3 volt batteries Then replace the battery compartment cover Device failures Please do not attempt to repair damaged devices yourself In case of further inquiries always state the model of your device as indicated on the back of the unit Body Clock TENS should be repaired by qualified technical personnel Body Clock TENS units are guaranteed for a period of 5 years against manufacturer s defects Note the guarantee is null and void if any attempt is made to open the unit by unauthorized personnel In the event of a fault please contact the supplier address found on the invoice or delivery note or Body Clock 108 George Lane South Woodford E18 1AD Tel 44 20 8532 9595 Fax 44 20 8532 9551 email salesObodyclock net Zon 2003 SGS e ISO 9001 2008 ISO 13485 2003 EC DIRECTIVE 93 42 EEC Annex V Body Clock Health Care Limited 108 George Lane South Woodford London E18 1AD England Tel 44 0 20 8532 9595 Fax 44 0 20 8532 9551 www bodyclock co uk 0120 e mail sales bodyclock net November 2013 2 C recycle This manual is recyclable
11. us Pro Technical Data MIN TYP MAX Operating Voltage 4 5V 6 0V 6 5V Output Intensity ohms 190UA 1 15mA Output Waveform Asymmetrical TIER rectangular Stimulation Pulse Rate 5 Hz 10 Hz 20Hz Pulse Width 0 15ms Low Battery Indication 4 1V 4 5V a oV Battery Life 30 sec cycle 8800 cycles Power Source Powered by 2 Lithium 3 volt batteries aa Weight grams 43 58 Dimensions 16 5cm x 3 7cm x 1 3cm 6 1 2 x 17 16 x 9 16 Classification This unit is fully compliant with EEC Directive 93 42 EEC and is classified as internally powered equipment Type BF It is intended for continuous operation Explanation of Symbols BF Isolated applied part Warning refer to accompanying documents i e this user manual Storage Temperature Range 5C 65 Storage Relative Humidity Up to 80 The radio shielding of the device has been ascertained according to VFG 243 1991 interference suppression of ISM devices Shapes of output curves under a 500 ohm load Max 12V 20 150us p 31 25ms 625ms Contraindications 1 This device should not be used around the Carotid sinus neck region or the orbits of the eyes Any use of this device on patients who have a demand type cardiac pacemaker Do not use this device transcere brally i e when treating another individual do not make a circuit by placing the device and your spare hand on their head The use of TENS whenever pain syn
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