AccuRelief ACRL-3001 Dual Channel Pain Relief Device User Manual

AccuRelief ACRL-3001 Dual Channel Pain Relief Device

This manual is valid for the AccuRelief™ Dual Channel Pain Relief Device ACRL-3001.
This instruction manual is published by Carex Health Brands. Carex Health Brands reserves the right to improve and amend this manual at any time without prior notice.
Amendments may however be published in new editions of this manual.

Conformity to safety standards
Carex Health Brands declares that the device complies with the following normative documents: IEC60601-1, IEC60601-1-2, IEC60601-2-10, IEC62366, IEC60601-1-11 ISO10993-5, ISO10993-10, ISO10993-1, ISO7010.

INTRODUCTION

Thank you for purchasing the AccuRelief™ Dual Channel Pain Relief Device (Model ACRL-3001) for your pain relief solution.
In order to use the stimulator safely, read the complete manual carefully before using the device for the first time.
Keep this instruction manual in a convenient place, or store with the device for future reference.
The AccuRelief™ Dual Channel Pain Relief Device is designed to be used for temporary relief of pain associated with sore and aching muscles in the shoulder, waist, back, neck, upper extremities (arm), and lower extremities (leg) due to strain from exercise or normal household work activities. It should be applied to normal, healthy, clean and dry skin of adult patients.

Standard Parts
The package contains the following components:

IMPORTANT SAFETY PRECAUTIONS AND WARNINGS

It is important that you read all the warnings and precautions included in this manual because they are intended to keep you safe, prevent injury and avoid a situation that could result in damage to the device.

SAFETY SYMBOLS USED IN THIS MANUAL
Indicates a potentially hazardous situation which, if not avoided, could result in death or serious injury.
Indicates a potentially hazardous situation which, if not avoided, could result in serious injury and equipment damage.
Indicates a potentially hazardous situation which, if not avoided, may result in minor or moderate injury to the user, or damage to the device or other property.

DANGER
This stimulator must not be used in combination with the following medical devices:

• Internally transplanted electronic medical devices, such as pacemakers.
• Electronic life-support equipment, such as respirators.
• Electronic medical devices attached to the body, such as electrocardiographs.
  Using this stimulator with other electronic medical devices may cause erroneous operation of those devices.

WARNING
Consult with your physician before using this device, because the device may cause lethal rhythm disturbances in certain susceptible individuals.
DO NOT USE THIS DEVICE UNDER THESE CONDITIONS:

• If you have a cardiac pacemaker, active implanted defibrillator, or other implanted metallic or electronic device. Such use could cause electric shock, burns, electrical interference, or death.ogether with a life-supporting medical electronic device such as an artificial heart, lung or respirator.
• In the presence of electronic monitoring equipment (e.g., cardiac monitors, ECG alarms), which may not operate properly when the electrical stimulation device is in use.
• On open wounds or rashes, over swollen, red, infected, inflamed areas, or skin eruptions (e.g., phlebitis, thrombophlebitis, varicose veins); or on top of, or in proximity to, cancerous lesions.
• Over areas of skin that lack normal sensation.
• On the opposite sides of your head since the effects of stimulation of the brain are unknown.

DO NOT USE ON THESE INDIVIDUALS:

• Pregnant women, because the safety of electrical stimulation during pregnancy has not been established.
• Children or infants, because the device has not been evaluated for pediatric use.
• Persons incapable of expressing their thoughts or intentions.

DO NOT USE THIS DEVICE DURING THESE ACTIVITIES:

• Bathing or showering;
• Sleeping;
• Driving, operating machinery or any activity in which electrical stimulation can put you at risk for injury.

PAIN MANAGEMENT WARNINGS

• If you have had medical or physical treatment for your pain, consult with your physician before using this device.
• If your pain does not improve, becomes seriously chronic or severe, or continues for more than five days, stop using the device and consult with your physician.
• The mere existence of pain functions as a very important warning telling us that something is wrong. Therefore, if you suffer from any serious illness, consult your physician in order to confirm that it is advisable for you to use this TENS unit.

WARNINGS AND PRECAUTIONS REGARDING THE PADS

• Apply pads to normal, healthy, clean, dry skin (of adult patients) because it may otherwise disrupt the healing process.
• If you experience any skin irritation or redness after a session, do not continue stimulation on that area of the skin.

NEVER APPLY THE PADS TO:

• The head or any area of the face.
• Any area of the throat because this can cause severe muscle spasms resulting in closure of the airway, difficulty breathing, or adverse effects on heart rhythm or blood pressure.
• Both sides of the thorax simultaneously (lateral or front and back), or across your chest because the introduction of electrical current may cause rhythm disturbances, which could be lethal.

CAUTION
WARNINGS AND PRECAUTIONS REGARDING THE PADS

• Do not bend or fold because the pad may not function properly. Place the pads onto the plastic film and then store in the sealed package when not in use.

• Do not apply ointment or any solvent to the pads or to your skin because it will keep the pads from functioning properly.

• The pads are already pre-gelled and will adhere to your skin.

• To avoid damage to the adhesive surface of the pads, put the pads only on the skin or on the plastic film provided.

• Place pads at least 2 inches apart on your skin.
  The pads should never touch each other.

• always place clean pads by the illustrations provided (Refer to pages 18 and 19 for electrode placement).

• Make sure the components are connected well and the pads are fixed on the part of the body you wish to treat or the therapy may not be effective.

DO NOT USE YOUR PADS THIS WAY:

• Pads should not touch each other when placed onto your skin.
• Do not place on your spine or backbone.
• Pad should not touch any metal object, such as a belt buckle, necklace or other jewelry made from metal.
• Pads should not be placed simultaneously on the soles of both feet.
• Pads should not be placed simultaneously on the calves of both legs.
• Do not share pads with another person. This may cause a skin irritation or infection. Pads are intended for use by one person.
• Do not place or relocate the pads while the device is on.
• Always turn the power off before removing or changing the pad location.
• Do not leave pads attached to the skin after treatment.

CAUTION WHILE USING THE TENS UNIT

• If the TENS unit is not functioning properly or you feel discomfort, immediately stop using the device.
• Do not use for any other purpose except as described in this manual.
• Do not insert the electrode plug into any place other than the jack on the main TENS unit.
• Do not mix alkaline and manganese batteries, as this will shorten the battery life.
• Do not pull on the electrode cord during treatment.
• Do not use the TENS device while wearing electronic devices such as watches as this may damage the device.
• Do not use near a cell phone as this may cause the TENS unit to malfunction.
• Do not bend or pull the end of the cord.
• When removing the cord from the device, hold the plug and pull.
• Replace the cord when broken or damaged.
• the size, shape and type of pads may affect the safety and effectiveness of electrical stimulation.
• The electrical performance characteristics of the pads may affect the safety and effectiveness of electrical stimulation.
• Using pads that are too small or incorrectly applied, could result in discomfort or skin burns.
• Do not throw the batteries into a fire. The batteries may explode.
• Dispose of the device, batteries, and components according to applicable legal regulations. Unlawful disposal may cause environmental pollution.

GENERAL PRECAUTIONS

• The long-term effects of electrical stimulation are unknown.
• Apply stimulation to only normal, intact, clean, dry, and healthy skin.
• tENS is not effective in treating the original source or cause of the pain, including headache.
• TENS is not a substitute for pain medications and other pain management therapies.
• TENS devices do not cure disease or injuries.
• TENS is a symptomatic treatment and, as such, suppresses the sensation of pain that would otherwise serve as a protective mechanism.
• Effectiveness is highly dependent upon patient selection by a practitioner qualified in the management of pain patients.
• You may experience skin irritation or hypersensitivity due to the electrical s simulation or electrical conductive medium (gel) on the electrodes.
• If you have suspected or diagnosed heart disease, you should follow precautions recommended by your physician.
• If you have suspected or diagnosed epilepsy, you should follow precautions recommended by your physician.
• Use caution if you have a tendency to bleed internally, such as following an injury or fracture.
• Consult with your physician prior to using the device after a recent surgical procedure, because stimulation may disrupt the healing process.
• This stimulation should not be applied over the menstruating or pregnant uterus.
• This stimulation should not be applied over areas of skin that lack normal sensation.
• Keep unit away from young children. The unit contains small pieces that may be swallowed. Contact your physician immediately if ingested.
• For best results use this device with the AccuRelief™ brand electrodes and lead wires.
• Keep unit out of the reach of young children. The electrode cord can cause strangulation.

POSSIBLE ADVERSE REACTIONS

• Do not use device to treat one region for extended periods (more than 30 minutes a session, up to 3 times/day) or muscles in that region may become exhausted and sore.
• You may experience skin irritation and burns beneath the stimulation electrodes applied to your skin.
• You should stop using the device and consult with your physician if you experience adverse reactions from using the device.

ADDITIONAL CAUTIONS:

• Do not use this device over your eyes, mouth, face, front of neck (especially in the carotid sinus) head, upper back, or across your heart because this could cause severe muscle  spasms resulting in closure of your airway, difficulty breathing or adverse effects on heart rhythm or blood pressure.
• Do not use this device over, or in proximity to cancerous lesions.
• o not operate in close proximity (e.g. 1m) to shortwave or microwave therapy equipment as it may produce instability in the simulator output.
• This device should not be applied on or across your head or face since the effects of stimulator of the brain are unknown.
• Use this device with caution if you have a tendency to bleed internally, such as following an injury or fracture.
• Consult with your physician prior to using this device after a recent surgical procedure, because stimulation may disrupt the healing process.
• Do not use this device for pain of the central origin, including headache.
• this device is not to be used in the presence of flammable or anesthesia gasses.
• This product is not intended to be used during physical activity as interrupting the current by moving the electrode could result in shock.
• The electrode should not be applied to the skin for long periods of time or when not in use otherwise this could result in skin irritation.”

What is it?
The Dual Channel Pain Relief Device ACRL-3001 is a two output channel TENS machine and is highly effective in relieving pain. TENS is now regularly recommended by doctors, physiotherapists and pharmacists throughout the world.

HOW TENS WORKS FOR PAIN RELIEF
Transcutaneous Electrical Nerve Stimulation (TENS) is a noninvasive, drug-free method of controlling pain. TENS uses tiny electrical impulses sent through the skin to the nerves to modify pain perception. TENS does not cure any physiological problem. It only helps control the pain. TENS does not work for everyone. However, in most patients, it is effective in reducing or eliminating the pain, allowing for a return to normal activity.

How TENS works?
Scientific theory suggests that electrical stimulation therapy may work in several ways:

• the gentle electrical pulses move through the skin to nearby nerves to block the pain messagefrom the source of pain from ever reaching the brain.
• The gentle electrical pulses increase the production of endorphins, the body’s natural pain killer.

PACKAGE CONTENTS

KNOW YOUR DEVICE

Features

• Two output channels TENS stimulator, allowing for the option of two or four electrodes. The lead wires insert into Channel 1 and Channel 2 and each wire connects to two electrodes. The intensity of each pair of electrodes can be adjusted independently, and it is not necessary to have both channels running (you can use just one wire with two electrodes).
• ACRL-3001 offer six (6) programs (P1~P6) for you to choose from plus an additional six (6) PE preset programs that are suitable for different parts of the body and pain.
• 25 intensity levels of therapy, one (1) low intensity to 25 high intensity.

Front and rear panel

LCD Display

INSERTING BATTERIES

1. Remove the battery cover on the back of the device as shown by the graphic to the right.
2. Insert 3 x AAA batteries. Make sure the positive + and negative – signs correspond with the markings in the device when inserting batteries. Reinstall the battery cover as shown by the graphic to the right.

Notes:

1. Please use 3 x AAA batteries in this TENS unit.
2. Remove the batteries if the device is not in use for long periods.
3. Do not mix old and new batteries or different types of batteries.
4. Remove exhausted batteries from the unit.
5. warning: If batteries leak and come into contact with the skin or eyes, wash immediately with large amounts of water.
6. Batteries must be handled by an adult. Keep batteries out of the reach of children.
7. Dispose the used batteries safely according to local regulations.

ATTACHING THE BELT CLIP

1. To attach the belt clip to the device, simply slide
2. the clip up into the two connecting points until you hear a click.
3. To remove the belt clip from the device, simply slide the belt clip down.

EASY STEPS TO START YOUR THERAPY WITH ELECTRODE PADS

STEP 1
Attach pads to the lead wires Lead wire snaps onto the connector in the middle of the electrode pad.

STEP 2
Insert lead wires into the TENS unit Hold the lead wire plug and insert it into the socket on the top of the stimulator, as shown by the graphic to the right.

STEP 3
Pad placement
Remove the clear plastic film from the pack of the pads. Place pads on clean, dry and healthy skin, near or surrounding the pain at least 2 inches apart, and do not let them touch. Be sure there is a linear path between the pads.

Single Channel Electrode Placement
The AccuRelief™ Dual Channel Pain Relief Device features one or two channels for pain relief. When using only one channel and one set of electrodes, use the following placement guide:

NECK / CERVICAL PAIN
Attach both pads on the neck. (Do not place on the carotid artery or throat.)
SHOULDER PAIN
Attach one pad in front and one= in back of the muscle.
CARPAL TUNNEL / HAND PAIN
Attach both pads to the hand where you feel pain.
LOWER BACK / LUMBAR PAIN
Attach both pads on the lower back with the backbone in the center. Do not place on the backbone or spine.
ELBOW PAIN
Attach both pads on either side of the joint with the pain.
UPPER ARM PAIN
Attach both pads on either side of the region where you feel pain.

WARNING: Make sure the device is turned off or the intensities are set to zero (0) levels before placing pads on skin. Never remove the self-adhesive electrodes from the skin while the device is turned on.

KNEE / JOINT PAIN
Attach both pads above the knee or above and below the joint with pain.
CALF PAIN
Attach both pads on the calf/leg where you feel pain. Do not place electrode pads simultaneously to the calves of both legs. Treat one calf at a time.
ANKLE / FOOT PAIN
Attach pads per the illustration on the left for pain on the outside of your ankle/foot. Attach the pads per the illustration on the right for pain on the inside of your ankle/foot. Do not place electrode pads simultaneously to the soles of both feet. Treat one at a time.

Dual Channel Electrode Placement
The AccuRelief™ Dual Channel Pain Relief Device features one or two channels for pain relief. When using two channels and two sets of electrodes, use the following placement guide:

NECK / CERVICAL PAIN
Attach both sets of pads on the neck. (Do not place on the carotid artery or throat.)
SHOULDER PAIN
Attach one set of pads in front and one set in back of the muscle.
CARPAL TUNNEL / HAND PAIN
Attach both sets of pads on the hand where you feel pain.
LOWER BACK / LUMBAR PAIN
Attach both sets of pads on the lower back with the backbone inthe center. Do not place on the backbone or spine.
ELBOW PAIN
Attach both sets of pads on either side of the joint with the pain.
UPPER ARM PAIN
Attach both sets of pads on either side of the region where you feel pain.
WARNING: Make sure the device is turned off or the intensities are set to zero (0) levels before placing pads on skin. Never remove the self-adhesive electrodes from the skin while the device is turned on.
KNEE / JOINT PAIN
Attach both sets of pads above the knee or above and below the joint with pain.
CALF PAIN
Attach both sets of pads on the calf/leg where you feel pain. Do not place electrode pads simultaneously to the calves of both legs. Treat one calf at a time.
ANKLE / FOOT PAIN Attach pads per the illustration on the left for pain on the outside of your ankle/foot. Attach the pads per the illustration on the right for pain on the inside of your ankle/foot. Do not place electrode pads simultaneously to the soles of both feet. Treat one at a time.

STEP 4
Turn on the device Press the button to turn on the device. The following screen will appear:

STEP 5
Choose your treatment program
This device is equipped with two groups of programs (P & PE) to treat different body parts and pain. Press the P button to select one of the 6 therapy programs or Press the PE button to select a preset program for the body part you wish to treat. Please refer to page 25 for detailed program information. We recommend you choose a PE program first to begin with.

• STEP 5a
  Preset program selection
  The AccuRelief™ Dual Channel Pain Relief Device offers six (6) PE preset programs that correspond to a selected body part. Please refer to page 25 for detailed program information. Press the PE button to select the body part you want to treat. The  indicator will point to corresponding treatment part as follows:

• STEP 5b
  Program selection
  The AccuRelief™ Dual Channel Pain Relief De vice offers six (6) programs (P1~P6) for you to select from. Different programs suit different parts of the body. Please refer to page 25 for detailed program information. Press the P button to cycle and select from programs P1~ P6. Note: If you switch programs (either P or PE programs) during treatment, the device automatically resets the intensity to zero (0) and the treatment time to 30 minutes

STEP 6
Start treatment and adjust intensity Press s or t button to adjust the output intensity. The simulator will start to work. The maximum output intensity level is 25.

Setting the intensity
Intensity is based upon your level of comfort. Begin the first session with a low intensity and a short duration while learning how to operate the device. Therefore, caution should be used when working with maximum intensities ( i.e., always at the limit of what you can support.) Do not exceed your comfort level.

CAUTION:

• If the electrodes are not placed firmly on skin, or the device is not connected with the electrodes, and the output intensity level is over 5, the intensity will stop automatically.
• If the stimulation levels are uncomfortable or become uncomfortable, reduce the stimulation intensity to a comfortable level and contact your medical practitioner if problems persist.
• If your pain does not improve and you become sore from over-use, refrain from treating those areas for two (2) days. If this issue reoccurs, reduce the treatment time and intensity settings for future treatment.
• If you feel pain, dizziness, discomfort or nausea, call your physician or medical practitioner.
• Caution should be used when working with maximum intensities, (i.e., always at the limit of what you can support.) Do not exceed your comfort level.

STEP 7
Turn off the device
Press the button and hold for five (5) seconds to turn off the device. If there is no operation in the panel for two (2) minutes in the waiting state, the device will turn off automatically.

OTHER IMPORTANT FUNCTIONS IN THIS STIMULATOR

Safety Lock Feature
The lock function automatically activates after there is no operation in the panel for 30 seconds, and will be indicated by the display on the LCD. This is a safety feature to prevent accidental changes to your settings and to prevent accidental increase to the output intensity level. Press button to unlock.
Low battery indicator
When the low power indicator flashes on LCD, you should replace the batteries as soon as possible. The device will continue to operate for several more hours.

PROGRAM LIST

Program| Waveform description| Treatment location| Treatment duration
---|---|---|---
P1| Modulation| Shoulder| 30 min
P2| Burst| Hand / wrist| 30 min
P3| Continuous + burst| Lower back / waist| 30 min
P4| Deep TENS| Joint – knee / elbow| 30 min
P5| Modulation| Leg – thigh / calf / ankle / foot| 30 min
P6| Modulation| Neck| 30 min
PE-NECK| Alternate Ramped Burst (ARB)| Neck| 30 min
PE-SHOULDER| Simple Modulated Pulse (SMP)| Shoulder| 30 min
PE-HAND| Simple Modulated Pulse (SMP)| Hand / wrist| 30 min
PE-BACK| Modulated Amplitude (MA)| Lower back / waist| 30 min
PE-JOINTS| Alternate Ramped Burst (ARB)| Joint – knee / elbow| 30 min
PE-LEG| Modulated Amplitude (MA)| Leg – thigh / calf / ankle / foot| 30 min

SPECIFICATIONS

• Power sources: 4.5V DC, 3xAAA batteries
• Frequency: 2Hz~150Hz
• Pulse width: 50μs~330μs
• Output voltage: 0~90mA
• Output intensity level: 0~25 levels
• Treatment time: about 30 minutes
• Operating Conditions: 41°F~104°F (5°C~40°C); 30%RH~75%RH
• Storage and Transportation Conditions: 14°F~131°F (-10°C~55°C); 10%RH~90%RH
• Size: 117mm x 60mm x 34mm
• Weight: about 75.5g (without batteries)
• Service life   of the device: 3 years
• sservice life of battery: with new super heavy duty batteries, approx. 15 days when used for 30 min/day in P02 program at 13 level intensity.

HOW TO CONTROL AND REDUCE YOUR PAIN

When should the device be used?
Use as soon as your pain begins. Start with one session. The unit automatically turns off at 30 minutes. If you treat your pain early, it may prevent the pain from becoming worse, or even chronic. It is better to get pain under control sooner so you do not reach such a high pain threshold that it limits your daily activities.
How to choose the treatment program?
This device supplies two groups of programs to treat different parts of the body and pain. Each treatment part has two treatment programs. For instance, P6 and PE-NECK can be used for treatment of neck pain. If your pain does not improve, and you become sore from over-use after the cycle, choose the other program for future treatment. Normally, we recommend you use PE programs first.

How long should you use the device?
Start with one 30-minute session. Always turn unit off with pads still adhered to the skin. Rate your pain to check your progress, (1) low to (25) high. Intensity is based upon your level of comfort. Begin the first session with a low intensity and a short duration while learning how to operate the device. Stop the therapy session if pain has reduced or stopped. If your pain does not improve and you become sore from over-use, refrain from treating those areas for two (2) days. If this issue reoccurs, reduce the treatment time and intensity settings for future treatment.

Recommended treatment sessions as follows:

When to stop using device

1. If you experience an adverse reaction— skin irritation/redness / burns, headache or other painful sensation— or if you feel any unusual discomfort.
2. If your pain does not improve, becomes seriously chronic and severe, or continues for more than five (5) days.
   NOTE:
   If you feel pain, dizziness, discomfort or nausea, call your physician or medical practitioner.

What type of pain is TENS best for?
This therapy works best on acute pain because it is localized. Acute pain occurs in one area for less than three (3) months. If you have chronic pain, you may have pain in more than one area and for longer than six (6) months. Chronic pain may be compounded by other issues that this device cannot address.
Remember this device does not cure your pain or the original cause of the pain. It provides temporary relief or reduction of pain so that you can control your life and activities better.

Specific applications (Practical recommendations)

improvement is observed after the first week of use.
Neuralgia of upper limb| 1 week, 1x/day minimum, then adapt according to how the pain develops.| P2| According to requirements, the program can be repeated a number of times during the same day.
Muscular pain in the thoracic back region| 4 weeks, 2x/day, with a 10 minute break between the 2 sessions| P3| You are advised to consult your doctor if no improvement is observed after the first week of use.
Muscular pain in the low back region| 4 weeks, 2x/day, with a 10 minute break between the 2 sessions| P3| You are advised to consult your doctor if no improvement is observed after the first week of use.
Elbow pain| 1 weeks, 2x/day, then adapt according to how the pain develops.| P4| According to requirements, the program can be repeated a number of times during the same day.
Localized contracture in external side of the calf| 1 week, 1x/day| P5| Consult your doctor if no improvement is observed after the first week of use.

CLEANING AND STORAGE

Cleaning the unit

1. Turn unit off and disconnect the lead wires from the unit.
2. Clean the device after use with a soft, slightly moistened cloth. Wipe gently.
   • Do not use chemicals (like thinner, benzene).
   • Do not let water get into the internal area.

Note:

1. This device and accessories do not require sterilization.

Cleaning the electrode pads

1. Turn the power off and remove the lead wires from the pads.

2. Wash the pads when the adhesive surface becomes dirty and/or the pads are difficult to attach.
   Wash the pad softly with your fingertips under slow-running cold water for several seconds (do not use a sponge/cloth/sharp object like a nail on the adhesive side. Do not use detergents, chemicals or soap).

3. Dry the pads and let the adhesive surface air-dry completely (do not wipe with a tissue paper or cloth).

CAUTION:

• The life of pads may vary by the frequency of washing, skin condition, and storage state.
• If the pad no longer sticks to your skin or the pad is broken, you should replace them with new pads. AccuRelief™ Universal Supply Kit (ACRL-0001, ACRL-0021 or ACRL-0031). Before applying the self-adhesive electrodes, it is recommended to wash and degrease the skin, and dry it.
• Do not turn on the device when the electrodes are not positioned on the body.
• Never remove the self-adhesive electrodes from the skin while the device is still turned on.
• If replacement electrodes are necessary, use only electrodes that are the same size (2 in. x 2 in.) as the electrodes provided with the device.
• Use of electrodes that are larger may reduce the effect of the stimulation. Use of electrodes that are much smaller than the electrodes provided with the device may increase the chance of skin irritation or electrode burns occurring under the electrodes.
• Always use electrodes that have been cleared for marketing in the U.S. by the FDA.

Storing the electrode pads and lead wires

• Turn the device off and remove the lead wires from the unit.
• Remove the pad from your body and pull out lead wires from the pads.
• Place the pads on the plastic film and store in the sealed package.
• Wrap the lead wires and store in the sealed package.

Storing the unit

• Place the unit, electrodes, lead wires and manual back into gift box. Store the box in a cool, dry place, 14°F~131°F (-10°C~55°C); 10%~90% relative humidity.
• Do not store in places that can be easily reached by children.
• When not in use for a long period, remove the batteries before storage to avoid liquid discharge from batteries.

DISPOSAL
Used fully discharged batteries must be disposed of in a specially labeled collection container, at a toxic waste collection point or through an electrical retailer. You are under legal obligation to dispose of batteries correctly.
Please dispose of the device in accordance with local regulations.

TROUBLESHOOTING

If the unit does not operate after taking these measures, contact the nearest dealer.

polarity.

Stimulation weak or cannot feel any stimulation

| Electrodes are dried out or dirty.| Replace with new electrodes.
Electrodes do not stick to skin well.| Replace with new electrodes.
Lead wires are old, worn, or damaged.| Replace with lead wires.

Stimulation is uncomfortable

| Intensity is too high| Decrease intensity.
Electrodes are too close together.| Reposition electrodes to be at least 2 inches apart.
Electrode active area size is too small.| Replace electrodes with ones that have an active area no less than 4 in2 (2 in x 2 in.)
Is the device being operated according to the manual?| Please check the manual before use.
PROBLEM| POSSIBLE CAUSES| POSSIBLE SOLUTION
---|---|---

Intermittent output

|

Lead wires

| Verify connection is secure. Insert wires firmly.
Turn down the intensity. Rotate lead wires in socket 90°. If still intermittent, replace lead wire.
If still intermittent after replacing lead wire, a component may have failed. Call the repair department.

Stimulation is ineffective.

| Improper electrode placement.| Reposition electrode.
Unknown| Contact clinician.

The skin becomes red and/or you feel a stabbing pain

| Using electrodes on the same site every time.| Reposition the electrodes. If at any time you feel pain or discomfort, stop use immediately.
Electrodes are not adhered to the skin properly.| Ensure the electrodes are securely adhered to the skin.

The electrodes are dirty.

| Clean the electrodes according to description in this manual or replace with new electrodes.
The surface of the electrode is scratched.| Replace with new electrodes.

Output current stops during therapy

| The electrodes come off the skin.| Turn off the device and place the electrodes on again, or replace with new electrodes.
The lead wire is disconnected.| Turn off the device and connect the lead wires.
The batteries’ power has been exhausted.| Replace with new batteries.

IMPORTANT INFORMATION REGARDING ELECTROMAGNETIC COMPATIBILITY (EMC)

With the increased number of electronic devices such as computers and mobile (cellular) telephones, medical devices in use may be susceptible to electromagnetic interference from other devices. Electromagnetic interference may result in incorrect operation of the medical device and create a potentially unsafe situation. Medical devices should also not interfere with other devices.
In order to regulate the requirements for EMC (Electro Magnetic Compatibility) with the aim to prevent unsafe product situations, the IEC60601- 1-2 standard has been implemented. This standard defines the levels of immunity to electromagnetic interferences as well as maximum levels of electromagnetic emissions for medical devices. Medical devices manufactured by Carex Health Brands conform to this IEC60601-1-2:2007 standard for both immunity and emissions. Nevertheless, special precautions need to be observed:

• The use of accessories and cables other than those specified by Carex Health Brands, with the exception of cables sold by Carex Health Brands as replacement parts for internal components, may result in increased emission or decreased immunity of the device.

• The medical devices should not be used adjacent to or stacked with other equipment.
  In case adjacent or stacked use is necessary, the medical device should be observed to verify normal operation in the configuration in which it will be used.

• Refer to EMC table guidance regarding the EMC environment in which the device should be used.

TABLE 1:

GUIDANCE AND MANUFACTURER’S DECLARATION – ELECTROMAGNETIC EMISSIONS

AccuRelief™ electrical stimulators are intended for use in the electromagnetic environment specified below. The customer or the user of these electrical stimulators should assure that it is used in such environment.
Emissions test| Compliance| Electromagnetic environment – guidance
RF emissions CISPR 11| Group 1| The device uses RF energy only for its internal function. Therefore, its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment.
RF emissions CISPR 11| Class B| The device is suitable for use in all establishments, including domestic establishments and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purposes.
Harmonic emissions lEC 61000-3-2| Not applicable
Voltage fluctuations/ flicker emissions lEC 61000-3-3| Not applicable

TABLE 2:

GUIDANCE AND MANUFACTURER’S DECLARATION – ELECTROMAGNETIC IMMUNITY

AccuRelief™ electrical stimulators are intended for use in the electromagnetic environment specified below. The customer or the user of these electrical stimulators should assure that it is used in such environment.
Immunity test| IEC 60601 test level| Compliance level| Electromagnetic environment – guidance
Electrostatic discharge (ESD) lEC 61000-4-2| ±6 kV contact

±8 kV air

| ±6 kV contact

±8 kV air

| Floors should be wood, concrete or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30%.
Electrical fast transient/burst IEC 61000-4-4| Not applicable| Not applicable| Not applicable
Surge

IEC 61000-4-5

| Not applicable| Not applicable| Not applicable
Voltage dips, short interruptions and voltage variations on power supply IEC 61000-4-11| Not applicable| Not applicable| Not applicable
Power frequency (50/60Hz) magnetic field IEC 61000-4-8| 3 A/m| 3 A/m| Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment.
GUIDANCE AND MANUFACTURER’S DECLARATION – ELECTROMAGNETIC IMMUNITY

AccuRelief™ electrical stimulators are intended for use in the electromagnetic environment specified below. The customer or the user of these electrical stimulators should assure that it is used in such environment.
Immunity test| IEC 60601 test level| Compliance level| Electromagnetic environment – guidance

Conducted RF lEC 61000-4-6

Radiated RF lEC 61000-4-3

|

Not applicable

3 V/m

80 MHz to 2.5 GHz

|

3 V/m

| Portable and mobile RF

Communications equipment should be used no closer to any part of the device, including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter.

Recommended separation distance

d = 1.2 Ö P

d = 1.2 Ö P 80 MHz to 800 MHz

d = 2.3 Ö P 800 MHz to 2.5 GHz

Where P is the maximum output power rating of the transmitter in watts (w) according to the transmitter manufacturer and d is the recommended separation distance in meters (m).

 |  |  | Field strengths from fixed RF transmitters, as determined by an electromagnetic site survey, a __ should be less than the compliance level in each frequency range. b
 |  |  | Interference may occur in the vicinity of equipment marked with the following symbol:

NOTE I: At 80 MHz ends 800 MHz the higher frequency range applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.

• Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the device is used exceeds the applicable RF compliance level above, should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the device.
• Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.

RECOMMENDED SEPARATION DISTANCES BETWEEN

PORTABLE AND MOBILE RF COMMUNICATIONS EQUIPMENT AND THE DEVICE

This TENS device is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the TENS device can help prevent electromagnetic interference by

maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and as recommended below, according to the maximum output power of the communications equipment.

Output power of transmitter in watts| Separation distance according to frequency of transmitter in meters
150 kHz to 80 MHz

d = 1.2 Ö

| 80 MHz to 800 MHz

d = 1.2 Ö P

| 800 MHz to 2.5 GHz

d = 2.3 Ö P

0.01| 0.12| 0.12| 0.23
0.1| 0.38| 0.38| 0.73
1| 1.2| 1.2| 2.3
10| 3.8| 3.8| 7.3
100| 12| 12| 23

For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the  transmitter in watts (w) according to the transmitter manufacturer.

• NOTE 1: At 80 MHz and 800 MHz. the separation distance for the higher frequency range applies.
• NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection fro structures, objects and people.
• Note: EMC tests conducted including attached electrode cord of 1.2 m length.

GLOSSARY OF SYMBOLS
Electrical devices are recyclable material and should not be disposed of with household waste after their useful  life. Help us protect the environmentand save resources by taking this device to the appropriate collection point. Please contact the organization responsible for waste disposal in your area if you have any.

WARRANTY

Please contact your dealer or the device center in case of a claim under the warranty. If you have to send in the unit, enclose a copy of your receipt and clearly state the defect. The following warranty terms apply:

1. The warranty period for the device is one year from date of purchase. In case of a warranty claim, the date of purchase has to be proven by means of the sales receipt or invoice.
2. Repairs under warranty do not extend the warranty period for the device or for the replacement parts.
3. The following is excluded under the warranty:
4. Liability for direct or indirect consequential losses caused by the unit is excluded even if the damage to the unit is accepted as a warranty claim.

LIMITED ONE YEAR WARRANTY

Your AccuRelief™ device is warranted for a period of 1 year from the date of original purchase. Electrodes and lead wires are excluded from this warranty. Carex Health Brands sells its products with the intent that they are free of defects in manufacture and workmanship if used in accordance with the instructions provided. We will, at our option, repair or replace without charge any device covered by the above warranties. These warranties extend only to Consumers and do not extend to Retailers. To obtain warranty service on your AccuRelief™ product, contact Customer Service by calling at 1-800-328-2935 for the repair center address and for the return shipping/handling fee. Enclose a letter with your name, address, phone number, model number, serial number, date of purchase, location of purchase and description of specific problem. Be sure to include your receipt as Proof of Purchase. Pack the product carefully to prevent damage in transit. Because of possible loss in transit, we recommend insuring the product with return receipt requested.

Carex Health Brands does not authorize anyone, including, but not limited to, Retailers, the subsequent consumer purchaser of the product from a Retailer or remote purchasers, to obligate Carex Health Brands in any way beyond the terms set forth herein. These warranties do not cover damage caused by misuse or abuse; accident; the attachment of any unauthorized accessory; alteration to the product; improper installation; unauthorized repairs or modifications; improper use of electrical/power supply; loss of power; dropped product; malfunction or damage of an operating part from failure to provide manufacturer’s recommended maintenance and storage; transportation damage; theft; neglect; vandalism; or environmental conditions; loss of use during the period the product is at a repair facility or otherwise awaiting parts or repair; replacement batteries or any other conditions whatsoever that are beyond the control of Carex Health Brands. These warranties are effective only if the product is purchased and operated in the country in which the product is purchased. A product that requires modifications or adoption to enable it to operate in any other country than the country for which it was designed, manufactured, approved and/or authorized, or repair of products damaged by these modifications is not covered under this warranty.
THESE WARRANTIES PROVIDED HEREIN SHALL BE THE SOLE AND EXCLUSIVE WARRANTIES. THERE SHALL BE NO OTHER WARRANTIES EXPRESSED OR IMPLIED INCLUDING ANY IMPLIED WARRANTY OF MERCHANTABILITY OR FITNESS OR ANY OTHER OBLIGATION ON THE PART OF THE COMPANY WITH RESPECT TO PRODUCTS COVERED BY THESE WARRANTIES. CAREX HEALTH BRANDS SHALL HAVE NO LIABILITY FOR ANY INCIDENTAL, CONSEQUENTIAL OR SPECIAL DAMAGES. IN NO EVENT SHALL THESE WARRANTIES REQUIRE MORE THAN THE REPAIR OR REPLACEMENT OF ANY PART OR PARTS WHICH ARE FOUND TO BE DEFECTIVE WITHIN THE EFFECTIVE PERIOD OF THESE WARRANTIES. NO REFUNDS WILL BE GIVEN. IF REPLACEMENT PARTS FOR DEFECTIVE MATERIALS ARE NOT AVAILABLE, CAREX HEALTH BRANDS RESERVES THE RIGHT TO MAKE PRODUCT SUBSTITUTIONS IN LIEU OF REPAIR OR REPLACEMENT.
These warranties do not extend to the purchase of opened, used, repaired, repackaged and/or resealed products including but not limited to sale of such products on Internet auction sites and/or sales of such products by surplus or bulk resellers. Any and all warranties or guarantees shall immediately cease and terminate as to any products or parts thereof which are repaired, replaced, altered, or modified, without the prior express or written consent of Carex Health Brands. These warranties provide you with specific legal rights. You may have additional rights which may vary from state to state. Because of individual state regulations, some of the above limitations and exclusions may not apply to you. For more information regarding our product line in the USA, please visit: www.accurelief.com

• AccuRelief™ Model: __
• Serial Number:__ _____
• Date of Purchase:_ ___
• Distributor:____ ___

Manufactured for:
Carex Health Brands A division of Compass Health Brands
Tel: 800-328-2935
[email protected]

FAQs

What is the AccuRelief ACRL-3001 Dual Channel Pain Relief Device?

The AccuRelief ACRL-3001 Dual Channel Pain Relief Device is a medical device designed to provide temporary relief of pain associated with sore and aching muscles in the shoulder, waist, back, neck, upper extremities, and other areas

How does the AccuRelief ACRL-3001 Dual Channel Pain Relief Device work?

The device uses Transcutaneous Electrical Nerve Stimulation (TENS) therapy, which involves the application of electrical pulses to the skin to block pain signals and provide relief

What is the power source of the AccuRelief ACRL-3001 Dual Channel Pain Relief Device?

The device is powered by DC4.5V, 3xAAA batteries

What are the key features of the AccuRelief ACRL-3001 Dual Channel Pain Relief Device?

The device offers six PE preset programs for different body parts, six therapy programs, and 25 intensity levels of therapy. It is equipped with dual channel functionality, allowing the use of two or four wired electrodes

How long does the AccuRelief ACRL-3001 Dual Channel Pain Relief Device provide pain relief?

The device delivers targeted and effective pain relief for 30 minutes with an auto shut-off feature

What are the recommended body parts for the AccuRelief ACRL-3001 Dual Channel Pain Relief Device?

The device is designed for temporary relief of pain associated with sore and aching muscles in various body parts, including the shoulder, waist, back, neck, upper extremities, and other areas

What is the recommended method for selecting a body part with the AccuRelief ACRL-3001 Dual Channel Pain Relief Device?

Users can choose a PE preset program for the body part they wish to treat or select one of the six therapy programs

What is the recommended intensity level for the AccuRelief ACRL-3001 Dual Channel Pain Relief Device?

The device offers 25 levels of adjustable intensity, allowing users to find a comfortable level of relief

What is the recommended method for adjusting the intensity of the AccuRelief ACRL-3001 Dual Channel Pain Relief Device?

Users can press the s or t button to adjust the output

What is the recommended method for storing the AccuRelief ACRL-3001 Dual Channel Pain Relief Device?

Users should store the device in a cool, dry place to prevent damage to the batter

What are the safety standards that the AccuRelief ACRL-3001 Dual Channel Pain Relief Device complies with?

The device complies with IEC60601-1 and IEC60601-1-2 normative documents

Video-AccuRelief ACRL-3001 Dual Channel Pain Relief Device

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