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 INTRODUCTION 4.7 Adjust the Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12
1.1 General information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 4.8 Adjust Timer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12
1.2 Caution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 4.9 Adjust Channel Amplitude . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12
1.3 Indications for use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 4.10 Turn Unit Off . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .13
1.4 Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-2 4.11 Portability . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .13
1.5 Precautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-3 4.12 Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .13
1.6 Adverse Reactions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 4.13 Care of Electrodes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .14
4.14 Care of Electrode cords . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .14
2 PRODUCT DESCRIPTIONS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-6
5 HANDLING AND STORAGE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .15
3 STIMULATION MODES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-8
6 SPECIFICATION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .15
4 INSTRUCTIONS FOR USE
4.1 Check Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 7 ACCESSORIES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .16
4.2 Connect electrodes to lead wires . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9
4.3 Connect lead wires to unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 8 TROUBLESHOOTING . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .17
4.4 Place electrodes on skin . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11
4.5 Select the mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11 9 WARRANTY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .18
4.6 Adjust the Pulse Width . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11
Contents
Chapter Page Chapter Page
1 INTRODUCTION 4.7 Adjust the Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12
1.1 General information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 4.8 Adjust Timer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12
1.2 Caution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 4.9 Adjust Channel Amplitude . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12
1.3 Indications for use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 4.10 Turn Unit Off . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .13
1.4 Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-2 4.11 Portability . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .13
1.5 Precautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-3 4.12 Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .13
1.6 Adverse Reactions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 4.13 Care of Electrodes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .14
4.14 Care of Electrode cords . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .14
2 PRODUCT DESCRIPTIONS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-6
5 HANDLING AND STORAGE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .15
3 STIMULATION MODES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-8
6 SPECIFICATION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .15
4 INSTRUCTIONS FOR USE
4.1 Check Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 7 ACCESSORIES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .16
4.2 Connect electrodes to lead wires . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9
4.3 Connect lead wires to unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 8 TROUBLESHOOTING . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .17
4.4 Place electrodes on skin . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11
4.5 Select the mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11 9 WARRANTY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .18
4.6 Adjust the Pulse Width . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11
1. INTRODUCTION
1.1 General information: 1.4.5 Stimulation should not be applied over swollen, infected, or inflamed areas or skin eruptions, e.g., phlebitis,
This TENS is a lightweight and portable medical device which can help to reduce pain and discomfort. It utilizes low thrombophlebitis, varicose veins, etc.
electric-current to stimulate muscle nerves to achieve the symptomatic relief of chronic intractable pain, post- 1.4.6 Stimulation should not be applied over, or in proximity to, cancerous lesions.
traumatic and post-surgical pain. 1.4.7 For external use only.
1.4.8 Do not use TENS on the eye area.
1.2. Cautions 1.4.9 This device should be used only under the continued supervision of a licensed medical practitioner.
Federal law (USA) restricts this device to sale by or on the order of practitioners licensed by the State in which they 1.4.10 Safety of TENS devices for use during pregnancy or delivery has not been established.
practice to use or order the use of the device. 1.4.11 Electronic equipment such as ECG monitors and ECG alarms may not operate properly when TENS is in use.
1.4.12 Apply the electrodes to clean, dry, and unbroken skin only.
1.3. Indications for use: 1.4.13 This device should not be used while driving, operating machinery, or during any activity in which
This device is used in symptomatic relief of chronic intractable pain, post-traumatic and post-surgical pain. involuntary muscle contractions may put the user at undue risk of injury.
1.4.14 This device should be kept out of the reach of children.
1.4 Warnings: 1.4.15 Keep electrodes separate during treatment. Electrodes in contact with each other could result in improper
1.4.1 The long-term effects of chronic electrical stimulation are unknown. stimulation or skin burns.
1.4.2 Stimulation should not be applied over the carotid sinus nerves, particularly in patients with a known
sensitivity to the carotid sinus reflex. 1.5 Precautions:
1.4.3 Stimulation should not be applied over the neck or mouth. Severe spasm of the laryngeal and pharyngeal 1.5.1 Caution should be used for patients with suspected or diagnosed heart problems.
muscles may occur and the contractions may be strong enough to close the airway or cause difficulty in 1.5.2 Caution should be used for patients with suspected or diagnosed epilepsy.
breathing. 1.5.3 Caution should be used in the presence of the following:
1.4.4 Stimulation should not be applied transthoracically in that the introduction of electrical current into the (a)When there is a tendency to hemorrhage following acute trauma or fracture
heart may cause cardiac arrhythmias. (b)Following recent surgical procedures when muscle contraction may disrupt the healing process.
2
1
1. INTRODUCTION
1.1 General information: 1.4.5 Stimulation should not be applied over swollen, infected, or inflamed areas or skin eruptions, e.g., phlebitis,
This TENS is a lightweight and portable medical device which can help to reduce pain and discomfort. It utilizes low thrombophlebitis, varicose veins, etc.
electric-current to stimulate muscle nerves to achieve the symptomatic relief of chronic intractable pain, post- 1.4.6 Stimulation should not be applied over, or in proximity to, cancerous lesions.
traumatic and post-surgical pain. 1.4.7 For external use only.
1.4.8 Do not use TENS on the eye area.
1.2. Cautions 1.4.9 This device should be used only under the continued supervision of a licensed medical practitioner.
Federal law (USA) restricts this device to sale by or on the order of practitioners licensed by the State in which they 1.4.10 Safety of TENS devices for use during pregnancy or delivery has not been established.
practice to use or order the use of the device. 1.4.11 Electronic equipment such as ECG monitors and ECG alarms may not operate properly when TENS is in use.
1.4.12 Apply the electrodes to clean, dry, and unbroken skin only.
1.3. Indications for use: 1.4.13 This device should not be used while driving, operating machinery, or during any activity in which
This device is used in symptomatic relief of chronic intractable pain, post-traumatic and post-surgical pain. involuntary muscle contractions may put the user at undue risk of injury.
1.4.14 This device should be kept out of the reach of children.
1.4 Warnings: 1.4.15 Keep electrodes separate during treatment. Electrodes in contact with each other could result in improper
1.4.1 The long-term effects of chronic electrical stimulation are unknown. stimulation or skin burns.
1.4.2 Stimulation should not be applied over the carotid sinus nerves, particularly in patients with a known
sensitivity to the carotid sinus reflex. 1.5 Precautions:
1.4.3 Stimulation should not be applied over the neck or mouth. Severe spasm of the laryngeal and pharyngeal 1.5.1 Caution should be used for patients with suspected or diagnosed heart problems.
muscles may occur and the contractions may be strong enough to close the airway or cause difficulty in 1.5.2 Caution should be used for patients with suspected or diagnosed epilepsy.
breathing. 1.5.3 Caution should be used in the presence of the following:
1.4.4 Stimulation should not be applied transthoracically in that the introduction of electrical current into the (a)When there is a tendency to hemorrhage following acute trauma or fracture
heart may cause cardiac arrhythmias. (b)Following recent surgical procedures when muscle contraction may disrupt the healing process.
2
1
 2. PRODUCT DESCRIPTIONS
(c)Over the menstruating or pregnant uterus 2.1 Front and Rear panel:
(d)Over areas of the skin which lack normal sensation.
Top View
1.5.4 Some patients may experience skin irritation or hypersensitivity due to the electrical stimulation or electrical Channel 1 On/Off and Channel 2 On/Off and
Amplitude Control Amplitude Control
conductive medium. The irritation can usually be reduced by using an alternate conductive medium, or
alternate electrode placement. Channel 1 Output Channel 2 Output
1.5.5 Electrode placement and stimulation settings should be based on the guidance of the prescribing Receptacle Receptacle
practitioner. Channel 1 Output Channel 2 Output
1.5.6 This device should be used only with the leads and electrodes recommended for use by the manufacturer. Front View Indicator Light Indicator Light
1.5.7 Isolated cases of skin irritation may occur at the site of the electrode placement following long-term
Back View
application.
1.5.8 Effectiveness is highly dependent upon patient selection by a person qualified in the management of pain- Amplitude Control Power Indicator
Light
afflicted patients.
1.5.9 If the stimulation levels are uncomfortable or become uncomfortable, reduce the stimulation amplitude to a Pulse Width
comfortable level and contact your physician if problems persist. Control Clip
Lid Cover
Timer Switch

1.6 Adverse Reactions: Mode Switch

1.6.1 Possible skin irritation or electrode burn under the electrodes may occur.
1.6.2 Possible allergic skin reaction to tape or gel may occur. Frequency Control

Battery Compartment

3 4
 2. PRODUCT DESCRIPTIONS
(c)Over the menstruating or pregnant uterus 2.1 Front and Rear panel:
(d)Over areas of the skin which lack normal sensation.
Top View
1.5.4 Some patients may experience skin irritation or hypersensitivity due to the electrical stimulation or electrical Channel 1 On/Off and Channel 2 On/Off and
Amplitude Control Amplitude Control
conductive medium. The irritation can usually be reduced by using an alternate conductive medium, or
alternate electrode placement. Channel 1 Output Channel 2 Output
1.5.5 Electrode placement and stimulation settings should be based on the guidance of the prescribing Receptacle Receptacle
practitioner. Channel 1 Output Channel 2 Output
1.5.6 This device should be used only with the leads and electrodes recommended for use by the manufacturer. Front View Indicator Light Indicator Light
1.5.7 Isolated cases of skin irritation may occur at the site of the electrode placement following long-term
Back View
application.
1.5.8 Effectiveness is highly dependent upon patient selection by a person qualified in the management of pain- Amplitude Control Power Indicator
Light
afflicted patients.
1.5.9 If the stimulation levels are uncomfortable or become uncomfortable, reduce the stimulation amplitude to a Pulse Width
comfortable level and contact your physician if problems persist. Control Clip
Lid Cover
Timer Switch

1.6 Adverse Reactions: Mode Switch

1.6.1 Possible skin irritation or electrode burn under the electrodes may occur.
1.6.2 Possible allergic skin reaction to tape or gel may occur. Frequency Control

Battery Compartment

3 4
Lid Cover Mode Switch
A panel covers the controls for Mode, Timer, Frequency & Pulse WIdth. Your medical professional may ask to set Set Normal (N), Burst(B), or Modulation(M) mode
these controls for you and request that you leave the cover in place.
Timer Switch
Amplitude Controls Set 30 minutes, 60 minutes, or Constant .
It controls the "INTENSITY" level of stimulating pulses. These controls located at the top of the unit regulate the
amplitude, or intensity, of the stimulation and are the ON/OFF CONTROL. The power indicator will light up with Frequency Control
green color when the unit is working. Adjust Frequency from 2 Hz to 150 Hz by turning the control

Caution: If the stimulation levels are uncomfortable or become uncomfortable, reduce the stimulation intensity to a comfortable level Pulse Width Control
and contact your physician if problems persist. Adjust Pulse Width from 60 µs to 250 µs by turning the control

Battery compartment
9 Voltage battery- 1 pc

5 6
Lid Cover Mode Switch
A panel covers the controls for Mode, Timer, Frequency & Pulse WIdth. Your medical professional may ask to set Set Normal (N), Burst(B), or Modulation(M) mode
these controls for you and request that you leave the cover in place.
Timer Switch
Amplitude Controls Set 30 minutes, 60 minutes, or Constant .
It controls the "INTENSITY" level of stimulating pulses. These controls located at the top of the unit regulate the
amplitude, or intensity, of the stimulation and are the ON/OFF CONTROL. The power indicator will light up with Frequency Control
green color when the unit is working. Adjust Frequency from 2 Hz to 150 Hz by turning the control

Caution: If the stimulation levels are uncomfortable or become uncomfortable, reduce the stimulation intensity to a comfortable level Pulse Width Control
and contact your physician if problems persist. Adjust Pulse Width from 60 µs to 250 µs by turning the control

Battery compartment
9 Voltage battery- 1 pc

5 6
3.STIMULATION MODES
The mode switch offers three stimulation modes. The mode switch is located 3.2 NORMAL Mode:
under the front lid cover and you can shift the "MODE" switch to adjust the The Normal mode produces a continuous train of impulses. The stimulation
mode. parameters are not automatically interrupted nor varied in any way. In this mode, the
Be sure that when adjusting these stimulation modes, the intensity (Amplitude) pulse rate (from 2 to 150Hz) and pulse width (from 60 to 250µs) are fully adjustable.
output controls are set to the minimum output positions. The normal mode is quite versatile because it may be applied with a variety of rate
and width settings.
3.1 BURST Mode:
The burst mode provides a "burst" of seven pulses. There are two bursts 3.3 Modulation Mode:
delivered per second. Pulse width shows decrease/ increase cycle of variation. For example, if pulse width is
set for the maximum output value (250µs), pulse width will decrease from 250µs to
125µs and then increase back to 250µs again in period of 4 seconds.

7 8
3.STIMULATION MODES
The mode switch offers three stimulation modes. The mode switch is located 3.2 NORMAL Mode:
under the front lid cover and you can shift the "MODE" switch to adjust the The Normal mode produces a continuous train of impulses. The stimulation
mode. parameters are not automatically interrupted nor varied in any way. In this mode, the
Be sure that when adjusting these stimulation modes, the intensity (Amplitude) pulse rate (from 2 to 150Hz) and pulse width (from 60 to 250µs) are fully adjustable.
output controls are set to the minimum output positions. The normal mode is quite versatile because it may be applied with a variety of rate
and width settings.
3.1 BURST Mode:
The burst mode provides a "burst" of seven pulses. There are two bursts 3.3 Modulation Mode:
delivered per second. Pulse width shows decrease/ increase cycle of variation. For example, if pulse width is
set for the maximum output value (250µs), pulse width will decrease from 250µs to
125µs and then increase back to 250µs again in period of 4 seconds.

7 8
4. INSTRUCTIONS FOR USE
NOTE: Always read this instruction manual before use. 4.3 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 lead wires are
inserted correctly. The unit has two output receptacles controlled by Channel 1 and Channel 2 Amplitude Control
4.1 Check Battery: knobs at the top of the unit. You may choose to use one channel with one pair of lead wires or both channels with
Insert a fresh 9V alkaline or rechargeable battery into the battery compartment. Make two pairs of lead wires. Using both channels gives the user the advantage of stimulating two different areas at the
sure you are installing the battery properly. The battery is inserted in the casing on the same time.
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
CONNECTING THE STIMULATOR Electrodes Pads
Angle"L"-shape
4.2 Connect electrodes to lead wires: plug
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 EN60601-1 and EN60601-2, such as with
CE mark, or which are legally marketed in the US under 510(K) procedure.

9 10
4. INSTRUCTIONS FOR USE
NOTE: Always read this instruction manual before use. 4.3 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 lead wires are
inserted correctly. The unit has two output receptacles controlled by Channel 1 and Channel 2 Amplitude Control
4.1 Check Battery: knobs at the top of the unit. You may choose to use one channel with one pair of lead wires or both channels with
Insert a fresh 9V alkaline or rechargeable battery into the battery compartment. Make two pairs of lead wires. Using both channels gives the user the advantage of stimulating two different areas at the
sure you are installing the battery properly. The battery is inserted in the casing on the same time.
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
CONNECTING THE STIMULATOR Electrodes Pads
Angle"L"-shape
4.2 Connect electrodes to lead wires: plug
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 EN60601-1 and EN60601-2, such as with
CE mark, or which are legally marketed in the US under 510(K) procedure.

9 10
4.4 Place electrodes on skin: 4.7 Adjust the Frequency:
Apply electrodes to the exact site indicated by your physician, following the instruction The frequency is adjustable 2~150Hz.
included with the electrodes labeling. Before applying electrodes, be sure the skin surface Turn Frequency Control to adjust Frequency to the setting recommended by your medical
over which electrodes are placed is thoroughly cleaned and dried. Make sure the professional.
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.

ADJUSTING THE CONTROLS 4.8 Adjust Timer:

The timer is adjustable: 30 minutes, 60 minutes, or Constant.
4.5 Select the mode: Shift TIMER switch to set the stimulation time recommended by your physician or therapist.
Shift "MODE" switch to set the stimulation mode recommended by your physician or
therapist. For details about stimulating waveform and sequences, please refer to Sec. 3
"Stimulation Modes". 4.9 Adjust Channel Amplitude:
Turn Channel 1 or 2 clockwise. Slowly turn the Channel control until you reach the setting
Caution: Consult your physician for your suitable stimulation mode. recommended by your medical professional. Repeat for the other channel, if both channels
are to be used.
4.6 Adjust the Pulse Width:
The pulse width is adjustable 60~250µs. Caution: If the stimulation levels are uncomfortable or become uncomfortable, reduce the stimulation
Turn Pulse Width Control to adjust pulse width to the setting recommended by your intensity to a comfortable level and contact your medical practitioner if problems persist.
medical professional.

11 12
4.4 Place electrodes on skin: 4.7 Adjust the Frequency:
Apply electrodes to the exact site indicated by your physician, following the instruction The frequency is adjustable 2~150Hz.
included with the electrodes labeling. Before applying electrodes, be sure the skin surface Turn Frequency Control to adjust Frequency to the setting recommended by your medical
over which electrodes are placed is thoroughly cleaned and dried. Make sure the professional.
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.

ADJUSTING THE CONTROLS 4.8 Adjust Timer:

The timer is adjustable: 30 minutes, 60 minutes, or Constant.
4.5 Select the mode: Shift TIMER switch to set the stimulation time recommended by your physician or therapist.
Shift "MODE" switch to set the stimulation mode recommended by your physician or
therapist. For details about stimulating waveform and sequences, please refer to Sec. 3
"Stimulation Modes". 4.9 Adjust Channel Amplitude:
Turn Channel 1 or 2 clockwise. Slowly turn the Channel control until you reach the setting
Caution: Consult your physician for your suitable stimulation mode. recommended by your medical professional. Repeat for the other channel, if both channels
are to be used.
4.6 Adjust the Pulse Width:
The pulse width is adjustable 60~250µs. Caution: If the stimulation levels are uncomfortable or become uncomfortable, reduce the stimulation
Turn Pulse Width Control to adjust pulse width to the setting recommended by your intensity to a comfortable level and contact your medical practitioner if problems persist.
medical professional.

11 12
4.10 Turn Unit Off: 4.13 Care of Electrodes:
Turn both Channel Amplitude controls to off. Unplug the electrode lead wires, grasping To avoid skin irritation and ensure good contact with skin, clean silicone rubber electrodes
them by the plug, not the cord. If treatment will be resumed shortly, the electrodes may be with soap and water frequently. The electrodes must be dried completely before using.
left on the skin. When the electrodes are 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 C E
CARE AND MAINTENANCE mark, or which are legally marketed in the US under 510(K) procedure.

4.11 Portability: 4.14 Care of Electrode cords:

Your unit is portable and may be clipped to a belt, shirt pocket, bra, or other clothing. Clean the electrode cords by wiping them with damp cloth. Coating them lightly with
talcum powder will reduce tangles and prolong the life.

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

13 14
4.10 Turn Unit Off: 4.13 Care of Electrodes:
Turn both Channel Amplitude controls to off. Unplug the electrode lead wires, grasping To avoid skin irritation and ensure good contact with skin, clean silicone rubber electrodes
them by the plug, not the cord. If treatment will be resumed shortly, the electrodes may be with soap and water frequently. The electrodes must be dried completely before using.
left on the skin. When the electrodes are 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 C E
CARE AND MAINTENANCE mark, or which are legally marketed in the US under 510(K) procedure.

4.11 Portability: 4.14 Care of Electrode cords:

Your unit is portable and may be clipped to a belt, shirt pocket, bra, or other clothing. Clean the electrode cords by wiping them with damp cloth. Coating them lightly with
talcum powder will reduce tangles and prolong the life.

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

13 14
5. HANDLING AND STORAGE
Keep this device in the carrying case and store it at room temperature. Stimulation Modes descriptions
Mode BURST NORMAL Modulation
6. SPECIFICATION Frequency 2~150Hz 2~150Hz, 2~150Hz
Pulse Width 60~250µs 60~250µs 60~250µs
Channel Dual channels, isolated between channels Cycle Time 0.5 Sec. Constant. 4 Secs.
Pulse Amplitude 0 ~ 80 mA = 0 ~ 40 volts, adjustable (at 500 ohm load) Loading: 500Ω
Pulse Frequency (Hz) 2 ~ 150 *All values have±10% tolerance.
Pulse Width (µs) 60 ~ 250
Waveform Asymmetric biphasic square pulse. 7 ACCESSORIES
Timer Control (mins) 30, 60, or Constant
Power Supply 9V DC square shape battery Self-Adhesive Electrodes 4 PCS.
Size (D x W x H) 1.0" x 2.4" x 3.6" (26 mm x 62 mm x 91 mm) 9 V Battery 1 PC.
Weight (including battery) 4.4 oz (126 g) Lead Wires 2 PCS.
Safety standard EN 60601-1, EN 60601-1-2, IEC 60601-2-10 Instruction Manual 1 PC.
Operation Ambient Temperature Range 50 ~ 95ºF (10 ~ 35ºC)
Operation Ambient Humidity Range 20 ~ 90% RH
Storage & Transportation Temperature Range 32 ~ 158º F (0 ~ 70ºC)
Storage & Transportation Humidity Range 20 ~ 90% RH
All values have ±10% tolerance.

15 16
5. HANDLING AND STORAGE
Keep this device in the carrying case and store it at room temperature. Stimulation Modes descriptions
Mode BURST NORMAL Modulation
6. SPECIFICATION Frequency 2~150Hz 2~150Hz, 2~150Hz
Pulse Width 60~250µs 60~250µs 60~250µs
Channel Dual channels, isolated between channels Cycle Time 0.5 Sec. Constant. 4 Secs.
Pulse Amplitude 0 ~ 80 mA = 0 ~ 40 volts, adjustable (at 500 ohm load) Loading: 500Ω
Pulse Frequency (Hz) 2 ~ 150 *All values have±10% tolerance.
Pulse Width (µs) 60 ~ 250
Waveform Asymmetric biphasic square pulse. 7 ACCESSORIES
Timer Control (mins) 30, 60, or Constant
Power Supply 9V DC square shape battery Self-Adhesive Electrodes 4 PCS.
Size (D x W x H) 1.0" x 2.4" x 3.6" (26 mm x 62 mm x 91 mm) 9 V Battery 1 PC.
Weight (including battery) 4.4 oz (126 g) Lead Wires 2 PCS.
Safety standard EN 60601-1, EN 60601-1-2, IEC 60601-2-10 Instruction Manual 1 PC.
Operation Ambient Temperature Range 50 ~ 95ºF (10 ~ 35ºC)
Operation Ambient Humidity Range 20 ~ 90% RH
Storage & Transportation Temperature Range 32 ~ 158º F (0 ~ 70ºC)
Storage & Transportation Humidity Range 20 ~ 90% RH
All values have ±10% tolerance.

15 16
8. TROUBLESHOOTING 9. WARRANTY
If your unit does not seem to operate correctly, refer to the chart below to determine what may * Unit: One year (12 months) from the date of the original consumer purchase.
be wrong. If 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
• "On" and "Battery Light" are dim. • None of indicators lights up. To obtain service from Chattanooga Group or the selling dealer under this warranty, a written claim must be made
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.
they set to values prescribed by Chattanooga Group shall not be held liable in any event for incidental or consequential damages. Some states do not
your medical professional? allow exclusion or limitation of incidental or consequential damages so the above limitation or exclusion may not
2. Are electrodes in proper position? apply to you
3. Check lead wires. Be sure all
connectors are firmly sealed.
4. Replace cord set with another to
check for broken wires.

17 18
8. TROUBLESHOOTING 9. WARRANTY
If your unit does not seem to operate correctly, refer to the chart below to determine what may * Unit: One year (12 months) from the date of the original consumer purchase.
be wrong. If 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
• "On" and "Battery Light" are dim. • None of indicators lights up. To obtain service from Chattanooga Group or the selling dealer under this warranty, a written claim must be made
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.
they set to values prescribed by Chattanooga Group shall not be held liable in any event for incidental or consequential damages. Some states do not
your medical professional? allow exclusion or limitation of incidental or consequential damages so the above limitation or exclusion may not
2. Are electrodes in proper position? apply to you
3. Check lead wires. Be sure all
connectors are firmly sealed.
4. Replace cord set with another to
check for broken wires.

17 18
 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