Instruction Manual
Contents
1. 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 6 kV contact 6 kV contact Floors should be wood concrete or ceramic tile discharge ESD 8 kV air 8 kV air If floors are covered with synthetic material the IEC 61000 4 2 relative humidity should be at least 30 Electrical fast Not applicable Not applicable Not applicable transient burst IEC 61000 4 4 Surge Not applicable Not applicable Not applicable IEC 61000 4 5 Voltage dips short Not applicable Not applicable Not applicable interruptions and voltage variations on power supply input lines IEC 61000 4 11 Power frequency 3 A m 3 A m Power frequency magnetic fields should be at 50 60Hz magnetic field levels characteristic of a typical location in a typical IEC 61000 4 8 commercial or hospital environment TABLE 4 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 is2. from date of purchase In case of a warranty normal wear and tear claim the date of purchase has to be proven by c RA 4 Liability for direct or indirect consequential means of the sales receipt or invoice losses caused by the unit is excluded even if the 2 Repairs under warranty do not extend the damage to the unit is accepted as a warranty warranty period either for the device or for the claim replacement parts 3 The following is excluded under the warranty All damage due to improper treatment e g non observance of the user instruction LIMITED ONE YEAR WARRANTY Your AccuRelief Wireless TENS devices and remote control are warranted for a period of 1 year from the date of original purchase Electrode pads 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
3. press the button to increase or the button to decrease the intensity NOTE There are 20 levels of intensity Explanation of LED indicator on gel pads units Steady solid light the unit is on Flashing the unit is in use Rapid flashing the unit is receiving STEP 5 Turn off the device You can turn device off in the following ways The device will turn off automatically after 30 minutes treatment time Press the button continuously until the LED light turns off Turn the device off by pressing the D button on the remote control PLEASE NOTE Be sure not to move the gel pads to another part of your body without turning off the power first Never stick the gel pads to each other Keep the gel pads clean and do not expose to heat or direct sunlight If the gel pads do not adhere to your body or are dirty rep ace with new electrodes Do not clean the pad or adhesive gels with any chemical Place the ge pads on intact skin only Do not place on cuts or damaged skin The AccuRe person use Place the ge ief Wireless TENS is for single pads on the protective transparent film when not in use information from the remote Light off the unit is switched off Front of Shoulder c Back of g Shoulder e e SHOULDER BACK ARM 20 MAINTENANCE AND CAUTIONS Do not immerse the the AccuRelief Wireless TENS ACRL 9000 in water or
4. 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 in 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 AN 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 o 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 the pads at least 2 inches apart on your skin The pads should never touch each other Always place clean pads in accordance with the illustr
5. x 17 7 H mm Unit A and B 42 5g without battery Remote control 44 4g without battery Unit A and B 3 years With new batteries approx 20 days if used for 30 min day in normal conditions NOTE Design and specifications are subject to change without notice PROGRAMI The AccuRelief ACRL 9000 unit is preset with a combination program that delivers three phases of alternating therapy They are specified as follows Phase Frequency Pulse width Time Description 1 80 125Hz 130 uS 5 min The frequency is changed in a cycle which is from 80Hz to 125Hz then back 80Hz The cycle time is 32s 2 5 10Hz 250 uS 20 min The frequency is changed in a cycle which is from 5Hz to 10Hz then back 5Hz The cycle time is 10s 3 80 125Hz 130 uS 5 min The frequency is changed in a cycle which is from 80Hz to 125Hz then back 80Hz The cycle time is 32s DISPOSAL Used fully discharged batteries must be disposed of in a specially labeled collection container at toxic waste collection points or through an electrical retailer You are under legal obligation to dispose of batteries correctly Please dispose of the device in accordance with appropriate laws TROUBLESHOOTING If the unit does not operate after taking these measures contact Carex Health Brands PROBLEM POSSIBLE CAUSES POSSIBLE SOLUTION The unit cannot power on Is the battery exhausted Replace the battery Is the battery i
6. any liquid Do not drop the device or throw it from a height After use remove the gel pads from the skin and place on the protective transparent film Always use the protective film when the gel pads are not in use Do not use any chemical to clean the device or the gel pads If you need to clean the unit please wipe with a damp lint free cloth Do not let the gel pads dry out or expose them to direct sunlight Keep the gel pads clean STORAGE After use disconnect the gel pads and then store safely and out of the reach of children Store the AccuRelief Wireless TENS ACRL 9000 in a cool dry place 10 C 55 C 1096 90 relative humidity Do not expose the gel pads to direct sunlight and protect them against dirt and moisture If the gel pads no longer stick to your skin or the gel pads are broken you should replace with new pads TECHNICAL SPECIFICATIONS Type Power supply Wave form Frequency Pulse width Output voltage Output intensity level Treatment time Operating conditions Storage and transportation conditions Size Weight Service life of the device Service life of batteries AccuRelief Wireless TENS ACRL 9000 6 x AAA Bi phase square pulse wave 5 125Hz 130 250 uS 0 70mA 0 20 levels 30 minutes 50 F 104 F 10 C 40 C 3096RH 8596RH 14 F 131 F 10 C 55 C 10 RH 90 RH 103 0 L x 55 8 W x 25 2 H mm Remote control 60 0 L x 53 0 W
7. 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 Tel 800 328 2935 customerservice carex com Z fl Copyright 2014 by Carex Health Brands
8. the EMC environment in which the device should be used 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 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 from structures objects and people Note EMC tests conducted including attached electrode cord of 1 5 m length EXPLANATION OF SYMBOLS Type BF Applied Part Disposal in accordance with Directive 2002 96 EC WEEE Refer to instruction manual because of the higher levels of output Caution D o I gt gt Keep dry WARRANTY Please contact Carex Health Brands or the All damage which is due to repairs or device center in case of a claim under the tampering by the customer or unauthorized warranty If you have to send in the unit third parties enclose a copy of your receipt and clearly Damage during transport from the state the defect The following warranty terms manufacturer to the consumer or during apply transport to the service center 1 The warranty period for the device is one year The battery and gel pads are subject to
9. 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 produ
10. AccuRetlef Wireless HENS Natural drug free pain relief 30 Minute Treatment With Remote Control User Manual EN Model ACRL 9000 This manual is valid for the AccuRelief Wireless TENS Pain Reliever ACRL 9000 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 All Rights Reserved Rev V2 0 2014 20140513 Conformity to safety standards Carex Health Brands declares that the device complies with the following normative documents IEC60601 1 IEC60601 1 2 EC60601 2 10 IEC62366 IEC60601 1 11 ISO10993 5 IS010993 10 ISO10993 1 ISO7010 TABLE OF CONTENTS nigoro leino a Peu T TE E Mm 4 mportant safety precautions and warnings sssri UU L U LI iiiar aans 6 Package COMEN Sansonha enn nag DEDOS Product structure Know your device Battery information Treatment information Gel pad ostio ti Cu char iae r tox a Rehd exe cx aco Fera d Rau RSEN ERE RA CEPAR RN Da S RAE RR REN EUREN AE Maintenance and cautions SOL Beo o virent Technical specifications mice O Belen E MOUGIESMOOUM OKs M mportant information regarding electromagnetic compatibility EMC Explanationm of syrmbolS certis L etra Pda sua ashuy Warranty INTRODUCTION Than
11. IONS If you have a cardiac pacemaker active DO NOT USE ON THESE INDIVIDUALS implanted defibrillator or other implanted metallic or electronic device Such use could cause electric shock burns electrical interference or death Together 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 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
12. 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 for 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 other than those specified by Carex Health Brands may result in TABLE 1 GUIDANCE AND MANUFACTURER S DECLARATION ELECTROMAGNETIC EMISSIONS AccuReliefTM 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 Group 1 The device uses RF energy only for its internal function Therefore its RF CISPR 11 emissions are very low and are not likely to cause any interference in nearby electronic equipment RF emissions Class B The device is suitable for use in all establishments other than domestic and those CISPR11 directly connected to the public low voltage power supply network that supplies 7 Ex buildings used for domestic purposes Harmonic emissions Not applicable IEC 61000 3 2 Voltage fluctuations Not applicable flicker emissions IEC 61000 3 3
13. ations provided Refer to page 20 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 he 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 reatment CAUTION WHILE USING THE TENS UNIT f 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 mix alkaline and manganese batteries as this will shorten the battery life Do not use the TENS device while wearing electronic devices such as watches as this may damage the device Do not throw the batteries into a fire The batteries may explode Dispose of the device batteries and components according to app
14. cts 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
15. ing of skin Clip excess hair from the treatment area and remove any jewelry that may come in contact with the stimulation of the device Wash area with soap and water and dry completely STEP2 Preparation of the TENS unit Each gel pad is pre fixed with a stud to connect to the back of the device and is protected by a transparent film Attach the gel pads to the back of the device pressing them in place STEP 3 Placing the gel pads If using only one gel pad for treatment remove the layer of protective transparent film and place that side of the gel pad to the skin positioning the gel pad on the area of pain If using both gel pads position them around the area of pain in a linear path at least 2 inches apart Press to ensure adhesion Please refer to page 20 to understand where to place gel pads for optimal treatment PLEASE NOTE GEL PADS ARE REPLACEABLE AccuRelief Supply Kit Item ACRL 0003 Affix gel pads so that they do not overlap one another and are approximately 2 inches apart STEP 4 Operating the TENS unit Once the gel pads are attached the TENS unit is ready to be switched on NOTE You cannot turn the gel pad units on by pressing the remote control 1 Press the button on the gel pad unit to turn the gel pad on A steady green light indicator light will turn on to let you know the gel pad is on 2 Using either the remote control or the gel pad units
16. k you for purchasing the AccuRelief Wireless TENS with Remote Model ACRL 9000 for your pain relief solution Please read the complete manual carefully before using the device for the first time and keep this instruction manual in a convenient place or store with the device for future reference The pain reliever ACRL 9000 is a TENS stimulator What is TENS TENS stands for Transcutaneous Electrical Nerve Stimulation It 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 does TENS work Scientific theory suggests that electrical stimulation therapy may work in several ways The gentle electrical pulses move through the skin to nerves nearby the source of pain shutting out the pain message from ever reaching the brain The gentle electrical pulses increase the production of endorphins the body s natural pain killer What conditions can TENS help relieve TENS provides pain relief for a number of different pain conditions associated with exercise normal work and household activities This product is designed for temporary relief of muscle and joint pain in the Neck Waist Shou
17. lder Upper Extremities arms Back Lower Extremities leg The pain reliever should be applied to normal healthy clean and dry skin of adult patients What can l treat The Pain Reliever can treat many different types of pain Refer to diagrams on page 20 for the ideal locations to place the gel pads for the treatment of the most common forms of pain For other areas of pain place the gel pads on either side of the pain area PLEASE NOTE Never place the gel pads on the head face heart chest area eyes oral cavity carotid arteries sexual organs or over the spine or bony premises How long can l use the Wireless TENS unit You may use the Wireless TENS unit for at least 30 minutes a day However initially you may need to wear it for longer Please seek medical advice If you wear it for longer periods please check your skin where the gel pads have been placed to ensure your skin does not become sore PLEASE NOTE The gel pads are designed for temporary use for approximately 10 days when used for 30 minutes a day The Wireless TENS ACRL 9000 contains the following components 6 x AAA battery 2 x Gel pads with 1 x Remote control snap connector Quick start guide 1 x User manual Draw string carry bag Gel pad units A amp B IMPORTANT SAFETY PRECAUTIONS AND WARNINGS are intended to keep you safe prevent injury and avoid a situation that could result in damage to It is important that you read all the warni
18. licable legal regulations Unlawful disposal may cause environmental pollution The size shape and type of pads may affect the safety and effectiveness of electrical stimulation Use only the AccuRelief brand electrodes AccuRelief Supply Kit ACRL 0003 designed specifically for the ACRL 9000 Wireless TENS device 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 diseases 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 stimulation 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 you
19. ng and precautions included in this manual because they the device DANGER This stimulator must not be used in combination with the following medical devices SAFETY SYMBOLS USED IN THIS MANUAL Indicates a potentially hazardous situation which if not avoided could result in death or serious injury Internally transplanted electronic medical Indicates a potentially hazardous situation devices such as pacemakers which if not avoided could result in Electronic life support equipment such as serious injury and equipment damage respirators Indicates a potentially hazardous situation Electronic medical devices attached to the body A which if not avoided may result in minor such as electrocardiographs or moderate injury to the user or damage Using this stimulator with other electronic medical to the device or other property 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 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 DO NOT USE THIS DEVICE UNDER effects of stimulation of the brain are unknown THESE CONDIT
20. not 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 b Over the frequency range 150 kHz to 80 MHz field strengths should be less than 3 V m TABLE 6 RECOMMENDED SEPARATION DISTANCES BETWEEN PORTABLE AND MOBILE RF COMMUNICATIONS EQUIPMENT AND THE DEVICE The device is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled The customer or the user of the 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 Rated maximum output Separation distance according to frequency of transmitter power of transmitter m w 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2 5 GHz d 1 2 V d 1 2 VP d 2 3 VP 0 01 0 12 0 12 0 23 0 1 0 38 0 38 0 73 1 1 2 1 2 2 3 100 12 12 23 increased emission or decreased immunity of the device Refer to EMC table guidance regarding
21. nstalled correctly nsert the battery observing polarity Stimulation weak or cannot feel any Gel pads are dried out or dirty Replace with new gel pads Reconnect the pads stimulation Gel pads cannot stick to skin well Stimulation is Intensity is too high Decrease intensity uncomfortable Is the device being operated according to the manual Please check the manual before use The skin becomes red and or you feel a stabbing pain Use the gel pads on the same site every time Re position the gel pads The gel pads are not sticking onto the skin properly Ensure the gel pads are securely placed on he skin The gel pads are dirty Replace with new gel pads The surface of the gel pads is scratched Replace with new gel pads IMPORTANT INFORMATION REGARDING ELECTROMAGNETIC COMPATIBILITY EMC 44 4g without battery Unit A and B NOTE Design and specifications are subject to change without notice 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 Electromagnetic Compatibility with the
22. r 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 LN The unit contains small pieces that may be swallowed Contact your physician immediately if ingested Use this device only with the AccuRelief brand electrodes POSSIBLE ADVERSE REACTIONS Do not use the device to treat one region for extended periods of time 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 PACKAGE CONTENTS Quick start guide TENS CELL k TENS CELL k 6 AAA Batteries j AccuRelief 7 j n ACRL 9000 unit Wireless t ul d SENS 1 F 8 J d t lt evant Instruction manual Electrode placement guide Wireless TENS PRODUCT STRUCTURE Power ON increase LED indicator intensity button Gel pad D n D 2 bu Power OFF decrease intensity button Battery cover Snap fastener Gel pad Uni
23. t A Gel pad Unit B KNOW YOUR DEVICE LED indicator Decrease intensity Increase intensity of gel pad unit A of gel pad unit A Decrease intensity Increase intensity of gel pad unit B of gel pad unit B Decrease intensity of both gel paq units A and B Increase intensity of both gel pad units A and B Power off button Battery cover BATTERY INFORMATION Before inserting battery please ensure the device has been turned off 1 With the unit separated from the gel pad remove the battery cover from back Insert two AAA batteries making sure to match the and ends of the batteries to those in unit Replace the back cover and snap the electrode gel pad onto the gel pad unit If using both gel pad units please repeat steps 1 2 for the 2nd gel pad unit WARNING Remove the batteries if the device is not in use for long periods of time Keep battery out of the reach of children Dispose of the used battery safely according to local regulations bh If the battery leaks and comes into contact with the skin or eyes wash immediately with large amounts of water Standard for battery replacement If you feel the stimulation intensity is weak or the device cannot power on the batteries may be exhausted If so please replace the batteries TREATMENT INFORMATION Do not mix old and new batteries or different types of batteries STEP 1 Clean
24. used in such environment Immunity test Conducted RF IEC 61000 4 6 Radiated RF IEC 61000 4 3 IEC 60601 test level Not applicable 3 V m 80 MHz to 2 5 GHz Compliance level 3 V m Electromagnetic environment guidance 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 2vP d 1 2 VP 80 MHz to 800 MHz d 2 3 VP 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 should be less than the compliance level in each frequency range C Interference may occur in the vicinity of equipment marked with the following symbol NOTE At 80 MHz ends 800 MHzZ 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 a 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 can
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