LUMISCOPE 2000-T Operation Manual

Transcutaneous Electrical
Nerve Stimulation
(TENS) Device
Model 2000-T
Operation Manual
Read this manual before operating the TENS device. Save this manual for future reference.
CONTENTS
IntroductIon..................................................................3
Safety...............................................................................5
contentS.of.thIS.2000-t.kIt Product.SPecIfIcatIonS InStructIonS.for.uSInG.the.2000-t uSInG.eLectrodeS: SkIn.care: carInG.for.the.2000-t trouBLeShootInG: Warranty
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Packaging, warranties, products, and specications are
subject to change without notice. GF Health Products, Inc. is not responsible for typographical errors.
2000-T TENS 2
INTRODuCTION
Indications
This device is restricted to sale or use by or on the order of a physician licensed in the state in which he or she is practicing. It is to be used solely for the symptomatic relief of chronic in­tractable pain.
Contraindications
1. Do not place the TENS electrodes over the carotid artery (neck) region.
2. Patients with implanted electronic devices (for example, a pacemaker) or metallic im­plants should not undergo TENS treatment without rst consulting a physician.
3. Do not apply the TENS electrodes so that current passes transcerebrally (through the head).
4. The use of TENS whenever pain symptoms are undiagnosed and the etiology has not been established.
To the Patient
You have been diagnosed as having a type of pain discomfort that may be alleviated by the use of transcutaneous electrical nerve stimulation. The
2000-T TENS 3
2000-T generates electrical pulses that are sent through the electrodes which are placed over nerve centers. The various pulses employed by 2000-T can block pain signals normally sent to the brain through nerve bers, thereby inter­rupting the brain’s awareness of pain. The 2000-T may activate the release of endorphins which are chemicals used by the body to suppress pain naturally.
Transcutaneous Electrical Nerve Stimulation (TENS) is:
- Safe.
- Non-invasive.
- Non-pharmaceutical.
- Non-addictive.
Many clinical studies have shown the effective­ness of TENS for the relief of pain. Your 2000-T can reduce the need for pharmaceuticals if used as prescribed by your physician. Abide by the warnings and contraindications listed in this manual when undergoing TENS treatment.
2000-T TENS 4
SafETy
WarnInG:.Indicates.a.potential.hazard.situ­ation.or.unsafe.practice.that,.if.not.avoided,. could.result.in.death.or.serious.personal. injury.
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Caution: Indicates a potential hazard or un­safe practice that, if not avoided, could result in minor personal injury or product/property damage.
Warnings
WarnInG:.the.safety.of.tenS.devices.for. use.during.pregnancy.or.delivery.has.not. been.established.
WarnInG:.the.effectiveness.of.tenS.for. pain.of.central.origin,.such.as.for.headaches. has.not.been.established.
WarnInG:.tenS.devices.should.be.used. only.under.the.continued.supervision.of.a. physician.
WarnInG:.tenS.devices.have.not.been. established.to.have.curative.value.
WarnInG:.tenS.is.a.symptomatic.treat­ment,.and.as.such.suppresses.then.sensa­tion.of.pain.which.would.otherwise.serve.as. a.protective.mechanism.
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WarnInG:.tenS.devices.must.be.kept.out. of.reach.of.children.
WarnInG:.tenS.may.interfere.with.elec­tronic.monitoring.equipment.such.as.ecG. monitors.and.ecG.alarms.
PLEASE READ THIS MANUAL COMPLETELY AND CAREFULLY BEFORE USING THE TRANS­CUTANEOUS ELECTRICAL NERVE STIMULATOR (TENS).
CONTENTS Of ThIS 2000-T kIT
Qty Description
One 2000-T unit One Set of electrodes Two Sets of wire leads One 9V battery One Operation Manual One Carrying case
PRODuCT SPECIfICaTIONS
Channels Two Power
Source
One 9V disposable battery, or One 9V rechargeable NiCad battery
2000-T TENS 6
Wave Form Rectangular, constant current alternating
biphasic with “0” net DC component
Pulse
Variable, 2-120Hz
Frequency Pulse Width Variable, 40-260u sec Charge per
80mA X 250u sec: 20uC, 500 ohm test load
Pulse Maximum
80mA
Current: Mode Normal
Mode
Adjustable pulse width and frequency, with constant repetition of pulses.
Pulse Burst Mode
2 bursts per second, 7 pulses per burst, with 100Hz intraburst rate. Only the pulse width remains adjustable.
Modulation Mode
Contains a gradual pulse rise time and fall time, cycling on 4 seconds, with adjustable pulse width and frequency.
Power
Lit when in use Indicator Lights
Output
Lit at channel outlet being used Indicator Light
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All values have ±10% tolerance
INSTRuCTIONS fOR uSING ThE 2000-T
1. The ON/OFF switches are the amplitude control knobs located on the top of the unit. There are two amplitude control knobs: Channel 1 and Channel 2. The unit is set to the OFF position when this knob is set to 0. If one of the knobs is set to a position other than 0, the correspond­ing channel is currently in the ON position. The amplitude increases in intensity as the control knob is moved from 1 to 8. Each channel operates independently from the other. Turn­ing ON one channel gives a steady fast ashing yellow power indicator light located next to the channel. A green light located between the two amplitude control knobs will light up when the unit is in the ON position. A weak battery is indicated when this light becomes dim.
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2. Set the Pulse Frequency Control. This regu­lates the frequency of the pulses from 2 to 120 pulses per second (pps or Hz).
3. Set the Pulse Width Control. This regulates the width (duration) of each pulse from 40 to 260 micro seconds.
4. Set the Mode Selector Switch to one of the three modes of stimulation:
M Modulation Mode: This mode cycles every
4 seconds. The pulse width and frequency remain adjustable.
B Burst Mode: This mode produces two
bursts of pulses every second. Each burst has 7 pulses; each pulse at the 100Hz rate. The pulse width remains adjustable.
N Normal Mode: This mode provides a
steady stream of pulses. The pulse width and pulse frequency remain adjustable.
5. Setting the Pulse Width and Pulse Frequency:
a. Conventional settings: set the pulse width
to 90 to 100 microseconds.
b. Low rate settings: Set the pulse width to
200 to 220 microseconds. Set the pulse frequency to 2 to 4 Hz.
c. Brief intensity settings: Set the pulse width
to 200 to 250 microseconds.
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6. Holding the insulated portion of the lead wire plug, push the plug into one of the channel output ports located on the top of the unit; one or two sets of wires may be used. (The lead wires have one end which inserts into the electrodes and one end which inserts into the channel output port.)
7. Batteries: Use
ONLY 9V or 9V rechargeable
NiCad batteries with this unit.
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Caution: Effectiveness of TENS treatment is highly dependent upon patient selection by a qualified physician.
2000-T CONTROL DIaGRaM:
2000-T TENS 10
uSING ELECTRODES:
To maximize comfort while using electrodes the following measures are recommended:
1. Before applying or removing electrodes turn the unit to the OFF position using the Ampli­tude Control Knobs.
2. Read and follow the instructions for use for the electrodes utilized.
3. Place the electrode onto the skin over the desired nerve ber region. Note: If a compo­nent of the electrode is not afxed to the skin a tingling sensation may occur at the spot of poor contact which may cause discomfort. Be sure the entire electrode is rmly in place.
4. Insert the lead wire into the Channel Output Receptacle after the electrode is applied.
Suggestions:
Never remove an electrode while the unit is in the ON position. This may cause an uncomfort­able tingling sensation to occur.
Never disconnect either end of a wire lead by pulling on the wire. Disconnect the lead wire by holding the insulated portion of the lead wire end.
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Caution: Skin irritation may occur at the elec­trode site following long-term application.
SkIN CaRE:
To reduce the chance of skin irritation, the fol­lowing is recommended:
1. Closely clip or shave hair before applying an electrode to encourage better contact and connectivity between the skin and the elec­trode.
2. Only apply clean electrodes to clean dry skin.
3. Firmly press the electrode onto the skin to en­sure complete contact is achieved. If a compo­nent of the electrode is not afxed to the skin a tingling sensation may occur at the spot of poor contact which may cause discomfort.
4. When removing the electrode, pull GENTLY on the electrode.
5. Do not apply an electrode over broken skin as this may produce discomfort.
6. When applying an electrode, do not allow the skin or the electrode to be stretched.
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Caution: Improper application of electrodes or TENS settings my cause electrode burns. Use the TENS unit as directed by your physi­cian.
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CaRING fOR ThE 2000-T
1. When not in use, store the 2000-T in the case provided to protect it from external damage.
2. Make sure the electrode and the skin are both clean.
3. Firmly press the electrode onto the skin to ensure complete surface contact is achieved. If a component of the electrode is not afxed to the skin a tingling sensation may occur at the spot of poor contact which may cause discomfort.
4. When removing the electrode, pull GENTLY on the electrode.
5. Do not apply an electrode over broken skin as this my produce discomfort.
6. When applying an electrode, do no allow the skin or the electrode to be stretched.
7. The 2000-T may be cleaned by wiping it gently with a damp cloth moistened with mild soap and water. Never immerse the device in water or other liquids. The lead wires may be cleaned with a damp cloth moistened with soap and water.
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Caution: Improper application of electrodes or TENS settings my cause electrode burns. Use the TENS unit as directed by your physi­cian.
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TROuBLEShOOTING:
If the TENS unit does not function properly:
1. Make sure the battery is properly installed or replace the battery.
2. If the Channel Amplitude knobs are turned to the OFF position and there is a light blinking or glowing do not use the unit. Contact an authorized GF Health Products, Inc. represen­tative.
3. If the Channel Amplitude knobs are turned to the OFF position and any stimulation is felt do not use the unit. Contact an authorized GF Health Products, Inc. representative.
4. If the lights are functioning correctly and no stimulation is felt, check to ensure the lead wires are properly connected and the elec­trodes are in place. If the unit appears to be functioning and no stimulation is felt, the lead wires or electrodes may need to be replaced.
5. If any problems occur, contact an authorized GF Health Products, Inc. representative. Do not try to repair the unit.
Note: The life of a NiCad battery is about 12% as long as the life of an alkaline battery. At a medium setting, the battery life of an alkaline battery will be approximately 75 hours.
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WaRRaNTy
GF Health Products, Inc. warrants the Lumiscope 2000-T TENS Device for a period of ve years for defects in workmanship and materials. During the warranty period, defective items will be re­paired or replaced at manufacturer’s option at no charge. Any evidence of misuse, abuse, alterna­tions, or externally caused damage may void this warranty.
Batteries, electrodes, and/or lead wires are not covered by this warranty. This warranty guaran­tees you specic rights, but you may have addi­tional rights which vary from state to state.
For more information, please contact GF Health Products, Inc., at 800-672-8293.
Manufactured for GF Health Products, Inc. Atlanta, GA 30360, USA
Manufactured and Printed in China
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USA Corporate Headquarters:
GF Health Products, Inc.
2935 Northeast Parkway
Atlanta, Georgia 30360
telephone: 800-347-5678, 770-447-1609
fax: 800-726-0601, 678-291-3232
www.grahameld.com
© 2008 GF Health Products, Inc.
2000-T-INS-LAB-RevA08
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