Intelect TENS

77684C

Intelect TENS
®

77395A
2003 Encore Medical

Intelect TENS
®

77393A
2003 Encore Medical

Intelect IFC
®

77392A
2003 Encore Medical

Intelect NMES
®

77391A
2003 Encore Medical

Intelect NMES
®

77394A
2003 Encore Medical
Contents
Chapter Page Chapter Page
1 GENERAL INFORMATION 5.4 Place electrodes on skin . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11
1.1 What is a Neuromuscular Stimulator? . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 5.5 Adjust Contraction (ON) Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11
1.2 How does a Neuromuscular Stimulator work? . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 5.6 Adjust Relaxation (OFF) Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11
1.3 The Instrument . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 5.7 Select the Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12
5.8 Select the Ramp Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12
2 SAFETY 5.9 Adjust Channel Amplitude . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12
2.1 Caution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 5.10 Turn Unit Off . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .13
2.2 Indications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 5.11 Portability . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .13
2.3 Warning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 5.12 Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .13
2.4 Precaution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 5.13 Care of Electrodes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .14
2.5 Adverse Reactions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 5.14 Care of Electrode cords . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .14

3 TECHNICAL SPECIFICATIONS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 6 DO'S AND DON'TS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .15

4 CONTROLS AND INDICATORS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-8 7 HANDLING AND STORAGE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .16

5 INSTRUCTIONS FOR USE 8 ACCESSORIES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .16

5.1 Check Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9
5.2 Connect electrodes to lead wires . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 9 TROUBLESHOOTING . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .17
5.3 Connect lead wires to unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10
10 WARRANTY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .18
Contents
Chapter Page Chapter Page
1 GENERAL INFORMATION 5.4 Place electrodes on skin . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11
1.1 What is a Neuromuscular Stimulator? . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 5.5 Adjust Contraction (ON) Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11
1.2 How does a Neuromuscular Stimulator work? . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 5.6 Adjust Relaxation (OFF) Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11
1.3 The Instrument . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 5.7 Select the Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12
5.8 Select the Ramp Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12
2 SAFETY 5.9 Adjust Channel Amplitude . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12
2.1 Caution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 5.10 Turn Unit Off . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .13
2.2 Indications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 5.11 Portability . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .13
2.3 Warning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 5.12 Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .13
2.4 Precaution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 5.13 Care of Electrodes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .14
2.5 Adverse Reactions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 5.14 Care of Electrode cords . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .14

3 TECHNICAL SPECIFICATIONS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 6 DO'S AND DON'TS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .15

4 CONTROLS AND INDICATORS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-8 7 HANDLING AND STORAGE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .16

5 INSTRUCTIONS FOR USE 8 ACCESSORIES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .16

5.1 Check Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9
5.2 Connect electrodes to lead wires . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 9 TROUBLESHOOTING . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .17
5.3 Connect lead wires to unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10
10 WARRANTY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .18
1. GENERAL INFORMATION 2. SAFETY
1.1 What is a Neuromuscular Stimulator? 2.1 Caution:
Neuromuscular Stimulation is achieved by sending small electrical impulses through the skin to the underlying motor Federal law (USA) restricts this device to sale by or on the order of practitioners licensed by the State in which they
units (nerves and muscles) to create an involuntary muscle contraction. practice to use or order the use of the device.
Neuromuscular stimulation has many uses beyond its traditional application to prevent disuse atrophy, including:
● An increased range of motion: As a substitute for passive stretching exercise performed by the patient or therapist. 2.2 Indications:
● Muscle re-education: for example, teaching patients how to set their quads. This NMES is intended to be used in:
1. Relaxation of muscle spasm.
1.2 How does a Neuromuscular Stimulator work? 2. Prevention or retardation of disuse atrophy.
Because the transdermal stimulation of nerves and muscles may be accomplished by electrical pulses, this modality 3. Increase local blood circulation.
can help prevent disuse atrophy. Accordingly, incapacitated patients can receive therapeutic treatment to create 4. Muscle re-education.
involuntary muscle contractions thereby improving and maintaining muscle tone without actual physical activity. 5. Immediate post surgical stimulation of calf muscles to prevent venous thrombosis.
6. Maintaining or increasing range of motion.
1.3 The Instrument:
The Neuromuscular Stimulator is an easy to use system. A marvel of miniaturized electronics, the lightweight power 2.3 Warnings:
unit transmits electrical pulses through the skin surface and stimulates motor units (nerve and muscles). The ● The long-term effects of chronic electrical stimulation are unknown.

electrical impulses are "ramped" so they closely emulate natural muscle contractions. ● Stimulation should not be applied over the carotid sinus nerves, particularly in patients with a known sensitivity to

the carotid sinus reflex.

● Stimulation should not be applied over the neck or 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.

1 2
1. GENERAL INFORMATION 2. SAFETY
1.1 What is a Neuromuscular Stimulator? 2.1 Caution:
Neuromuscular Stimulation is achieved by sending small electrical impulses through the skin to the underlying motor Federal law (USA) restricts this device to sale by or on the order of practitioners licensed by the State in which they
units (nerves and muscles) to create an involuntary muscle contraction. practice to use or order the use of the device.
Neuromuscular stimulation has many uses beyond its traditional application to prevent disuse atrophy, including:
● An increased range of motion: As a substitute for passive stretching exercise performed by the patient or therapist. 2.2 Indications:
● Muscle re-education: for example, teaching patients how to set their quads. This NMES is intended to be used in:
1. Relaxation of muscle spasm.
1.2 How does a Neuromuscular Stimulator work? 2. Prevention or retardation of disuse atrophy.
Because the transdermal stimulation of nerves and muscles may be accomplished by electrical pulses, this modality 3. Increase local blood circulation.
can help prevent disuse atrophy. Accordingly, incapacitated patients can receive therapeutic treatment to create 4. Muscle re-education.
involuntary muscle contractions thereby improving and maintaining muscle tone without actual physical activity. 5. Immediate post surgical stimulation of calf muscles to prevent venous thrombosis.
6. Maintaining or increasing range of motion.
1.3 The Instrument:
The Neuromuscular Stimulator is an easy to use system. A marvel of miniaturized electronics, the lightweight power 2.3 Warnings:
unit transmits electrical pulses through the skin surface and stimulates motor units (nerve and muscles). The ● The long-term effects of chronic electrical stimulation are unknown.

electrical impulses are "ramped" so they closely emulate natural muscle contractions. ● Stimulation should not be applied over the carotid sinus nerves, particularly in patients with a known sensitivity to

the carotid sinus reflex.

● Stimulation should not be applied over the neck or 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.

1 2
● Stimulation should not be applied transthoracically in that the introduction of electrical current into the heart may ● Electrode placement and stimulation settings should be based on the guidance of the prescribing practitioner.
cause cardiac arrhythmias. ● Stimulators should be kept out of the reach of children.
● Stimulation should not be applied over swollen, infected, or inflamed areas or skin eruptions, (e.g., phlebitis, thrombophlebitis, ● Stimulators should be used only with the leads and electrodes recommended for use by the manufacturer.

varicose veins, etc). ● Machinery Operation: Patient should never operate potentially dangerous machinery such as power saws,
● Stimulation should not be applied over, or in proximity to, cancerous lesions. automobiles, etc. during stimulation.
● Keep electrodes separate during treatment. Electrodes in contact with each other could result in improper

stimulation or skin burns. 2.5 Adverse Reactions:

● Possible skin irritation or electrode burn under the electrodes may occur.

2.4 Precautions: ● Possible allergic skin reaction to tape or gel may occur.
● Safety of powered muscle stimulators for use during pregnancy has not been established. ● If the stimulation levels are uncomfortable or become uncomfortable, reduce the stimulation amplitude to a
● Caution should be used for patients with suspected or diagnosed heart problems. comfortable level and contact your physician if problems persist.
● Caution should be used for patients with suspected or diagnosed epilepsy.
● Caution should be used in the presence of the following:

a. When there is a tendency to hemorrhage following acute trauma or fracture

b. Following recent surgical procedures when muscle contraction may disrupt the healing process
c. Over the menstruating or pregnant uterus
d. Over areas of the skin which lack normal sensation.
● Some patients may experience skin irritation or hypersensitivity due to the electrical stimulation or electrical

conductive medium. The irritation can usually be reduced by using an alternate conductive medium, or alternate
electrode placement.

3 4
● Stimulation should not be applied transthoracically in that the introduction of electrical current into the heart may ● Electrode placement and stimulation settings should be based on the guidance of the prescribing practitioner.
cause cardiac arrhythmias. ● Stimulators should be kept out of the reach of children.
● Stimulation should not be applied over swollen, infected, or inflamed areas or skin eruptions, (e.g., phlebitis, thrombophlebitis, ● Stimulators should be used only with the leads and electrodes recommended for use by the manufacturer.

varicose veins, etc). ● Machinery Operation: Patient should never operate potentially dangerous machinery such as power saws,
● Stimulation should not be applied over, or in proximity to, cancerous lesions. automobiles, etc. during stimulation.
● Keep electrodes separate during treatment. Electrodes in contact with each other could result in improper

stimulation or skin burns. 2.5 Adverse Reactions:

● Possible skin irritation or electrode burn under the electrodes may occur.

2.4 Precautions: ● Possible allergic skin reaction to tape or gel may occur.
● Safety of powered muscle stimulators for use during pregnancy has not been established. ● If the stimulation levels are uncomfortable or become uncomfortable, reduce the stimulation amplitude to a
● Caution should be used for patients with suspected or diagnosed heart problems. comfortable level and contact your physician if problems persist.
● Caution should be used for patients with suspected or diagnosed epilepsy.
● Caution should be used in the presence of the following:

a. When there is a tendency to hemorrhage following acute trauma or fracture

b. Following recent surgical procedures when muscle contraction may disrupt the healing process
c. Over the menstruating or pregnant uterus
d. Over areas of the skin which lack normal sensation.
● Some patients may experience skin irritation or hypersensitivity due to the electrical stimulation or electrical

conductive medium. The irritation can usually be reduced by using an alternate conductive medium, or alternate
electrode placement.

3 4
3. TECHNICAL SPECIFICATIONS 4. CONTROLS AND INDICATORS
Channel Dual channels, isolated between channels 2.1 Front and Rear panel:
Pulse Amplitude 0 ~ 80 mA = 0 ~ 40 volts, adjustable (at 500 ohm load) Knob Cover
Pulse Frequency (Hz) 5, 30, 100 Top View
Channel 1 On/Off and Channel 2 On/Off and
Pulse Width (µs) 250, fixed Amplitude Control Amplitude Control
Contraction (On) Time (sec) 1 ~ 30, adjustable
Channel 1 Output Channel 2 Output
Relaxation (Off) Time (sec) 1 ~ 45, adjustable Receptacle Receptacle
Waveform Asymmetric biphasic square pulse.
Timer Control (mins) No Channel 1 Output Channel 2 Output
Front View Indicator Light Indicator Light
Stimulation Mode One
Power Supply 9V DC square shape battery Back View
Knob Cover
Size (D x W x H) 1.0" x 2.5" x 3.6" (26 mm x 62 mm x 91 mm) Knob Cover
Amplitude Control Power Indicator
Weight (including battery) 4.4 oz (126 g) Light
Safety standard EN 60601-1, EN 60601-1-2, IEC 60601-2-10
Operation Ambient Temperature Range 50 ~ 95ºF (10 ~ 35ºC) Clip
Operation Ambient Humidity Range 20 ~ 90% RH Lid Cover
Storage & Transportation Temperature Range 32 ~ 158ºF (0 ~ 70ºC) Frequency Control
Contraction Time Switch
Storage & Transportation Humidity Range 20 ~ 90% RH
Control Relaxation Time
*All values have 10% tolerance.
Control
Ramp Control Battery Compartment
Switch

5 6
3. TECHNICAL SPECIFICATIONS 4. CONTROLS AND INDICATORS
Channel Dual channels, isolated between channels 2.1 Front and Rear panel:
Pulse Amplitude 0 ~ 80 mA = 0 ~ 40 volts, adjustable (at 500 ohm load) Knob Cover
Pulse Frequency (Hz) 5, 30, 100 Top View
Channel 1 On/Off and Channel 2 On/Off and
Pulse Width (µs) 250, fixed Amplitude Control Amplitude Control
Contraction (On) Time (sec) 1 ~ 30, adjustable
Channel 1 Output Channel 2 Output
Relaxation (Off) Time (sec) 1 ~ 45, adjustable Receptacle Receptacle
Waveform Asymmetric biphasic square pulse.
Timer Control (mins) No Channel 1 Output Channel 2 Output
Front View Indicator Light Indicator Light
Stimulation Mode One
Power Supply 9V DC square shape battery Back View
Knob Cover
Size (D x W x H) 1.0" x 2.5" x 3.6" (26 mm x 62 mm x 91 mm) Knob Cover
Amplitude Control Power Indicator
Weight (including battery) 4.4 oz (126 g) Light
Safety standard EN 60601-1, EN 60601-1-2, IEC 60601-2-10
Operation Ambient Temperature Range 50 ~ 95ºF (10 ~ 35ºC) Clip
Operation Ambient Humidity Range 20 ~ 90% RH Lid Cover
Storage & Transportation Temperature Range 32 ~ 158ºF (0 ~ 70ºC) Frequency Control
Contraction Time Switch
Storage & Transportation Humidity Range 20 ~ 90% RH
Control Relaxation Time
*All values have 10% tolerance.
Control
Ramp Control Battery Compartment
Switch

5 6
Knob Cover: Relaxation Time Control
An acrylic knob cover protects amplitude controls from accidental user touch when the unit is being used. After Adjust Relaxation Time from 1s to 45s by turning the control knob
adjusting the output, remember to have the cover closed.
Frequency Control Switch
Lid Cover: Select Frequency 5 Hz, 30 Hz, 100Hz by shifting the switch
A panel covers the controls for Frequency, Ramp, Contraction Time & Relaxation Time. Your medical professional
may ask to set these controls for you and request that you leave the cover in place. Ramp Control Switch
Select Ramp Time 1s, 3s, 5s by shifting the switch
Amplitude Controls:
It controls the "INTENSITY" level of stimulating pulses. These controls located at the top of the unit regulate the Battery compartment
amplitude, or intensity, of the stimulation and are the ON/OFF CONTROL. The power indicator will light up with 9 Voltage battery- 1 pc
green color when the unit is working.

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

Contraction Time Control

Adjust Contraction Time from 1s to 30s by turning the control knob.

7 8
Knob Cover: Relaxation Time Control
An acrylic knob cover protects amplitude controls from accidental user touch when the unit is being used. After Adjust Relaxation Time from 1s to 45s by turning the control knob
adjusting the output, remember to have the cover closed.
Frequency Control Switch
Lid Cover: Select Frequency 5 Hz, 30 Hz, 100Hz by shifting the switch
A panel covers the controls for Frequency, Ramp, Contraction Time & Relaxation Time. Your medical professional
may ask to set these controls for you and request that you leave the cover in place. Ramp Control Switch
Select Ramp Time 1s, 3s, 5s by shifting the switch
Amplitude Controls:
It controls the "INTENSITY" level of stimulating pulses. These controls located at the top of the unit regulate the Battery compartment
amplitude, or intensity, of the stimulation and are the ON/OFF CONTROL. The power indicator will light up with 9 Voltage battery- 1 pc
green color when the unit is working.

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

Contraction Time Control

Adjust Contraction Time from 1s to 30s by turning the control knob.

7 8
5. INSTRUCTIONS FOR USE
NOTE: Always read this instruction manual before use. 5.3 Connect lead wires to unit:
Before proceeding to this step, be sure the unit is completely turned OFF. Holding the insulated portion of the lead
PREPARATION FOR USE wire connector, insert the angled-"L" plug into the receptacle on the top of the main unit. Ensure the leads are
inserted correctly.
5.1 Check Battery: The unit has two output receptacles controlled by Channel 1 and Channel 2 Amplitude Control knobs at the top of
Insert a fresh 9V alkaline or rechargeable battery into the battery compartment. the unit. You may choose to use one channel with one pair of lead wires or both channels with two pairs of lead
Make sure you are installing the battery properly. The battery is inserted in the casing wires. Using both channels give the user the advantage of stimulating two different areas at the same time.
on the foot of the stimulator unit. BE SURE TO MATCH THE POSITIVE AND
NEGATIVE ENDS OF THE BATTERY TO THE MARKINGS IN THE
BATTERY COMPARTMENT OF UNIT.
Self-adhesive
Electrodes Pads
CONNECTING THE STIMULATOR Angle"L"-shape
plug

5.2 Connect electrodes to lead wires:

Insert the lead wire connector into electrodes connector (standard 0.08 inch female
connection). MAKE SURE THAT NO BARE METAL OF THE PINS IS
EXPOSED.

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

9 10
5. INSTRUCTIONS FOR USE
NOTE: Always read this instruction manual before use. 5.3 Connect lead wires to unit:
Before proceeding to this step, be sure the unit is completely turned OFF. Holding the insulated portion of the lead
PREPARATION FOR USE wire connector, insert the angled-"L" plug into the receptacle on the top of the main unit. Ensure the leads are
inserted correctly.
5.1 Check Battery: The unit has two output receptacles controlled by Channel 1 and Channel 2 Amplitude Control knobs at the top of
Insert a fresh 9V alkaline or rechargeable battery into the battery compartment. the unit. You may choose to use one channel with one pair of lead wires or both channels with two pairs of lead
Make sure you are installing the battery properly. The battery is inserted in the casing wires. Using both channels give the user the advantage of stimulating two different areas at the same time.
on the foot of the stimulator unit. BE SURE TO MATCH THE POSITIVE AND
NEGATIVE ENDS OF THE BATTERY TO THE MARKINGS IN THE
BATTERY COMPARTMENT OF UNIT.
Self-adhesive
Electrodes Pads
CONNECTING THE STIMULATOR Angle"L"-shape
plug

5.2 Connect electrodes to lead wires:

Insert the lead wire connector into electrodes connector (standard 0.08 inch female
connection). MAKE SURE THAT NO BARE METAL OF THE PINS IS
EXPOSED.

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

9 10
5.4 Place electrodes on skin:
Apply electrodes to the exact site indicated by your prescribing practitioner, following the 5.7 Select the Frequency:
instruction included with the electrodes labeling. Before applying electrodes, be sure the The Frequency setting has three options: 5Hz, 30Hz & 100Hz
skin surface over which electrodes are placed is thoroughly cleaned and dried. Make sure Shift "Frequency" switch to select the Frequency recommended by your physician or
the electrodes are placed firmly to the skin and make good contact between the skin and therapist.
the electrodes. Place the electrodes over the skin; attach them properly, firmly, and
evenly. 5.8 Select the Ramp Time:
The Ramp setting has three options: 1s, 3s & 5s
ADJUSTING THE CONTROLS Shift "Ramp" switch to select the Ramp Time recommended by your physician or therapist.
The special circuitry of the stimulator is designed so the electrical impulses gradually build
5.5 Adjust Contraction (ON) Time to a peak. This "ramped" pulse produces a gradual muscle contraction emulating natural
The Contraction (ON) Time is adjustable 1~30 seconds. muscle movement. It can also prevent spastic patients from reacting adversely.
Turn Contraction Time Control to adjust Contraction (ON) Time to the setting
recommended by your medical professional. 5.9 Adjust Channel Amplitude:
Turn Channel 1 or 2 clockwise. Slowly turn the channel control until you reach the setting
5.6 Adjust Relaxation (OFF) Time recommended by your medical professional. Repeat for the other channel if both channels
The Relaxation (OFF) Time is adjustable 1~45 seconds. are to be used.
Turn Relaxation Time Control to adjust Relaxation (OFF) Time to the setting Caution: If the stimulation levels are uncomfortable or become uncomfortable, reduce the stimulation
recommended by your medical professional. In order to prevent the spasticity, the intensity to a comfortable level and contact your physician if problems persist.
Relaxation Time can’t be adjusted less than the Contraction Time.

11 12
5.4 Place electrodes on skin:
Apply electrodes to the exact site indicated by your prescribing practitioner, following the 5.7 Select the Frequency:
instruction included with the electrodes labeling. Before applying electrodes, be sure the The Frequency setting has three options: 5Hz, 30Hz & 100Hz
skin surface over which electrodes are placed is thoroughly cleaned and dried. Make sure Shift "Frequency" switch to select the Frequency recommended by your physician or
the electrodes are placed firmly to the skin and make good contact between the skin and therapist.
the electrodes. Place the electrodes over the skin; attach them properly, firmly, and
evenly. 5.8 Select the Ramp Time:
The Ramp setting has three options: 1s, 3s & 5s
ADJUSTING THE CONTROLS Shift "Ramp" switch to select the Ramp Time recommended by your physician or therapist.
The special circuitry of the stimulator is designed so the electrical impulses gradually build
5.5 Adjust Contraction (ON) Time to a peak. This "ramped" pulse produces a gradual muscle contraction emulating natural
The Contraction (ON) Time is adjustable 1~30 seconds. muscle movement. It can also prevent spastic patients from reacting adversely.
Turn Contraction Time Control to adjust Contraction (ON) Time to the setting
recommended by your medical professional. 5.9 Adjust Channel Amplitude:
Turn Channel 1 or 2 clockwise. Slowly turn the channel control until you reach the setting
5.6 Adjust Relaxation (OFF) Time recommended by your medical professional. Repeat for the other channel if both channels
The Relaxation (OFF) Time is adjustable 1~45 seconds. are to be used.
Turn Relaxation Time Control to adjust Relaxation (OFF) Time to the setting Caution: If the stimulation levels are uncomfortable or become uncomfortable, reduce the stimulation
recommended by your medical professional. In order to prevent the spasticity, the intensity to a comfortable level and contact your physician if problems persist.
Relaxation Time can’t be adjusted less than the Contraction Time.

11 12
 5.13 Care of Electrodes:
5.10 Turn Unit Off: To avoid skin irritation and ensure good contact with your skin, clean silicone rubber
Turn both Channel Amplitude controls to "OFF" . Unplug the electrode lead wires, grasping them by the plug, not electrodes with soap and water frequently. The electrodes must be dried completely before
the cord. If treatment will be resumed shortly the electrodes may be left on the skin. When the electrodes are using.
removed, clean the skin thoroughly with mild soap and water. If there is skin irritation, consult your medical
professional. ❈ If you are using self-adhesive electrodes, disregard this procedure.
❈ Always use the electrodes with the requirements of the EN60601-1 and EN60601-2, such as with CE
mark, or are legally marketed in the US under 510(K) procedure.
CARE AND MAINTENANCE
5.14 Care of Electrode cords:
5.11 Portability: Clean the electrode cords by wiping them with a damp cloth. Coating them lightly with
Your unit is portable and may be clipped to a belt, shirt pocket, bra or other clothing. talcum powder will reduce tangles and prolong the life.

5.12 Battery:
To replace battery, open the lid cover and extract the battery. Replace with a 9 V alkaline
or similar rechargeable battery. Make sure you insert the battery correctly.

13 14
 5.13 Care of Electrodes:
5.10 Turn Unit Off: To avoid skin irritation and ensure good contact with your skin, clean silicone rubber
Turn both Channel Amplitude controls to "OFF" . Unplug the electrode lead wires, grasping them by the plug, not electrodes with soap and water frequently. The electrodes must be dried completely before
the cord. If treatment will be resumed shortly the electrodes may be left on the skin. When the electrodes are using.
removed, clean the skin thoroughly with mild soap and water. If there is skin irritation, consult your medical
professional. ❈ If you are using self-adhesive electrodes, disregard this procedure.
❈ Always use the electrodes with the requirements of the EN60601-1 and EN60601-2, such as with CE
mark, or are legally marketed in the US under 510(K) procedure.
CARE AND MAINTENANCE
5.14 Care of Electrode cords:
5.11 Portability: Clean the electrode cords by wiping them with a damp cloth. Coating them lightly with
Your unit is portable and may be clipped to a belt, shirt pocket, bra or other clothing. talcum powder will reduce tangles and prolong the life.

5.12 Battery:
To replace battery, open the lid cover and extract the battery. Replace with a 9 V alkaline
or similar rechargeable battery. Make sure you insert the battery correctly.

13 14
6. DO'S AND DON'TS 7. HANDLING AND STORAGE
A. DO: Keep this device in the carrying case and store at room temperature.
1. DO place the electrodes only as your clinician recommends.
2. DO keep the stimulator clean.
3. DO see your clinician if you have any problems or questions regarding your system. 8. ACCESSORIES
4. DO clean the cables only with water and mild soaps. DO NOT use rubbing alcohol or any other solvents.
5. DO remove the electrodes and discontinue stimulation if you experience skin irritation, until the source of that Self-Adhesive Electrodes 4 PCS.
irritation is determined by your clinician. 9 V Battery 1 PC.
6. DO turn both intensity knobs to "OFF" before replacing the battery. Lead Wires 2 PCS.
Instruction Manual 1 PC.
B. DON'T:
1. DO NOT damage your stimulator by bumping, dropping, or rough use.
2. DO NOT engage in contact sports when using your stimulator.
3. DO NOT get the stimulator wet. However, a damp cloth may be used for cleaning the outside only.
4. DO NOT pull or kink the cables.
5. DO NOT clean the cables with alcohol or Freon.
6. DO NOT allow electrode gel to get into the connector holes of the electrodes. DO NOT allow the electrodes
to touch each other during stimulation or improper stimulation and poor battery life will result.
7. DO NOT give the device to other individuals.
8. DO NOT store the unit at temperatures less than 32ºF (0ºC) or over 158ºF (50ºC).

15 16
6. DO'S AND DON'TS 7. HANDLING AND STORAGE
A. DO: Keep this device in the carrying case and store at room temperature.
1. DO place the electrodes only as your clinician recommends.
2. DO keep the stimulator clean.
3. DO see your clinician if you have any problems or questions regarding your system. 8. ACCESSORIES
4. DO clean the cables only with water and mild soaps. DO NOT use rubbing alcohol or any other solvents.
5. DO remove the electrodes and discontinue stimulation if you experience skin irritation, until the source of that Self-Adhesive Electrodes 4 PCS.
irritation is determined by your clinician. 9 V Battery 1 PC.
6. DO turn both intensity knobs to "OFF" before replacing the battery. Lead Wires 2 PCS.
Instruction Manual 1 PC.
B. DON'T:
1. DO NOT damage your stimulator by bumping, dropping, or rough use.
2. DO NOT engage in contact sports when using your stimulator.
3. DO NOT get the stimulator wet. However, a damp cloth may be used for cleaning the outside only.
4. DO NOT pull or kink the cables.
5. DO NOT clean the cables with alcohol or Freon.
6. DO NOT allow electrode gel to get into the connector holes of the electrodes. DO NOT allow the electrodes
to touch each other during stimulation or improper stimulation and poor battery life will result.
7. DO NOT give the device to other individuals.
8. DO NOT store the unit at temperatures less than 32ºF (0ºC) or over 158ºF (50ºC).

15 16
9. TROUBLESHOOTING 10. WARRANTY
If your unit does not seem to be operating correctly, refer to the chart below to determine what may be wrong. * Unit: One year (12 months) from the date of the original consumer purchase.
Should none of these measures correct the problem, the unit should be serviced. * Accessories (consisting of lead wire, AC adapter, electrodes, carrying case, and belt clip): 90 days from the date of
original consumer purchase.

• The power indicator lights up, but To obtain service from Chattanooga Group or the selling dealer under this warranty, a written claim must be made
• "On" and "Battery Light" are dim. • None of indicators light up.
unit does not function properly. within the warranty period to Chattanooga Group or the selling dealer.
1. Check all control settings. Are 1. Replace battery with a new one. 1. Replace battery with a new one.
Chattanooga Group shall not be held liable in any event for incidental or consequential damages. Some states do not
they set to values prescribed by
allow exclusion or limitation of incidental or consequential damages so the above limitation or exclusion may not
your medical professional?
apply to you.
2. Are electrodes in proper position?
3. Check lead wires. Be sure all
connectors are firmly sealed.
4. Replace cord set with another to
check for broken wires.

17 18
9. TROUBLESHOOTING 10. WARRANTY
If your unit does not seem to be operating correctly, refer to the chart below to determine what may be wrong. * Unit: One year (12 months) from the date of the original consumer purchase.
Should none of these measures correct the problem, the unit should be serviced. * Accessories (consisting of lead wire, AC adapter, electrodes, carrying case, and belt clip): 90 days from the date of
original consumer purchase.

• The power indicator lights up, but To obtain service from Chattanooga Group or the selling dealer under this warranty, a written claim must be made
• "On" and "Battery Light" are dim. • None of indicators light up.
unit does not function properly. within the warranty period to Chattanooga Group or the selling dealer.
1. Check all control settings. Are 1. Replace battery with a new one. 1. Replace battery with a new one.
Chattanooga Group shall not be held liable in any event for incidental or consequential damages. Some states do not
they set to values prescribed by
allow exclusion or limitation of incidental or consequential damages so the above limitation or exclusion may not
your medical professional?
apply to you.
2. Are electrodes in proper position?
3. Check lead wires. Be sure all
connectors are firmly sealed.
4. Replace cord set with another to
check for broken wires.

17 18
19
19
 Intelect TENS
®

77684C

Intelect TENS
®

77395A
2003 Encore Medical

Intelect TENS
®

77393A
2003 Encore Medical

Intelect IFC
®

77392A
2003 Encore Medical

Intelect NMES
®

77391A
2003 Encore Medical

Intelect NMES
®

77394A
2003 Encore Medical