MNP131 (I-TECH LA 500 ENG) - I
Contents
1. environment RF Emissions CISPR 11 RF Emissions CISPR 11 Harmonic emissions IEC 61000 3 2 Voltage fluctuations flicker emissions IEC 61000 3 3 Compliance Group 2 Class A Class A Complies Electromagnetic environment guidance The ME EQUIPMENT must emit electromagnetic energy in order to perform its intended function Nearby electronic equipment may be affected The ME EQUIPMENT is suitable for use in all establishments other than domestic establishments and those directly connected to the public low voltage power supply network that supplies buildings used for domestic purposes Guidance and manufacturer s declaration electromagnetic immunity FOR ALL ME EQUIPMENT The ME EQUIPMENT is intended for use in the electromagnetic environment specified below The customer or the user ofthe ME EQUIPMENT should assure that it is used in such an environment Electrostatic discharge ESD IEC 61000 4 2 Electrical fast transient burst IEC 61000 4 4 Sovra tensioni IEC 61000 4 5 Voltage dips short interruptions and voltage variations on power supply input lines IEC 61000 4 11 Power frequency 50 60Hz magnetic field IEC 61000 4 8 6kV 6kV contact contact 8kV air 8kV air 2kV for 2kV per power power supply lines supply lines input output lines line s to line s line s to line s earth earth lt 5 Ur gt 95 buco in Uy per 0 5 cicli lt 5 UT2. 300 ry ci i am ir Visa u AS a 5 i u 4 7 ia m After the set up of the power place the laser probe on the area to be treated and fasten it with the elastic belt MNPG127 01 Pag 10 1 TECK MEDICAL DIVISION In case of an emergency stop press the red button placed on the back of the machine After the treatment switch off the device moving the key switch on the OFF position upper picture Take away the key from the machine to avoid the use by unauthorized personnel Press the WAIT button to confirm all the adjusted values at this time it will be not Please do not switch off the device unplugging the cable from the power socket to possible to modify the treatment time and the power Press the START button to start avoid any type of damage to the device the treatment When the treatment will be finished the machine will emit an intermittent signal If you need to stop the treatment before the end press the STOP button and the device will stop immediately the laser emission Se Sern ao rare SS ee e Zu u gi MNPG127 01 Pag 11 MEDICAL DIVISION MAINTENANCE I TECH LA500 doesn t need any particular maintenance operation A periodic probe maintenance and cleaning is suggested in order to guarantee the optimal operating mode and consequently the treatment effectiveness and the patient safety The external
3. neurology dermatology rheumatology odontology conservative parodontology medical treatment by implants oral pathology surgery removal of tartar with pain and acupuncture crucial in acute chronic and degenerative inflammations such as knee arthritis I TECH LA500 carries out an important therapeutic action for the regeneration of chronic pathologies for the acceleration of the healing process in the acute pathology of edema inflammation Furthermore it is very effective in the fast resolution of painful articular muscle neurogenic syndromes and soft tissues Profondita di penetrazione cutanea della radiazione ottica UW 3 UV C UA Visibile Infrarosso Anm 200 00 400 590 690790 970 1200 bal ENT ee Y Tessin PRO ARREARS CLE LAO Ett Dede We MNPG127 01 Pag 7 MEDICAL DIVISION INTENDED USE I TECH LA500 is an electro medical device that delivers treatments of laser therapy with the help of power laser up to 500mW for the provision of treatment though a specific probe I TECH LA500 is an active therapeutic device not invasive used especially by physiotherapists physicians and pain therapists The use of I TECH LA500 is indicated for professional user in clinics hospitals and for home users in home environment The operator in fact should be qualified to be able to use such equipment and he should have passed an adapted training or should operate under the control of a medical adequately quali
4. the correctness of the electric installation of device before activating the supply switch It is advisable to suspend the therapeutic treatment if it were to appear some disturbances during its emission It s strongly advised not to hold the device on in state of start without using the probe it could overheat MNPG127 01 Pag 6 MEDICAL DIVISION INTRODUCTION OF THE TECNOLOGY The evolution of light The new Laser I TECH LA 500 is equipped with a new probe that allows beam laser application directly to the treatment area Thus you can make sure that the laser performs its therapeutic action as an impressive regenerative stimulation in chronic pathologies in the acceleration of the inflammation resolution and of the oedema in acute pathologies and in the rapid resolution of painful articular muscular neurogenal and soft tissues syndromes both acute and chronic I TECH LA500 allows an immediate improvement in the symptoms of inflammatory and degenerative pathologies in the orthopaedic neurologic dermatologic domain and a reduction of recovery times and presents itself as an indispensable therapy especially in Sports Medicine since it allows rapid recovery for many sportsmen for whom time is a determining factor in their career The advantages of Laser therapy Laser therapy is not based on the generation of heat but on photochemical and photo biological effects on cells and tissues Observations have shown that if
5. cleaning of the device must be done only using a wet soft cloth or not flammable liquid detergents The frontal panel can be cleaned in the same way Unplug the device from the electric socket anytime you decide to clean the machine To guarantee the best operation of the device in safety condition for the patient we suggest to send the machine to the manufacturer for a check up every two years The check up of the system must be done only by technicians authorized by the manufacturer because specific machines are needed We recommend to clean accurately the probe cover output lens using alcohol and a piece of cotton at the end of each treatment to avoid the steamed up and the incrustations of the lens Pay attention to not pour the liquids into the handle head All the liquids used for the cleaning of the machine must evaporate before starting a new treatment especially in case of flammable liquids to avoid any risk of fire caused by endogenous gas Store carefully the handles applicators at the end of each treatment HANDLES CLEANING The laser handle is very weak and it needs a daily cleaning The following advices are absolutely important to not damage the lens and the laser probe It is suggested to 1 Remove the dust using a soft cloth 2 Clean the area using neutral and not abrasive products 3 Dry it accurately using a cloth Do not twist the handle s cable Don t let any liquid penetrate into the holes Do n
6. negative environmental impact in consideration of their operational and safety requirements Rigorous standards were followed in order to minimize the amount of waste use of OA of the equipment BF toxic materials noise non required radiation and energy consumption Manufacturer A thorough research was carried out to design the unit so as to optimize power consumption in accordance with energy saving principles PA Manufactured the This symbol means that the product shall not be disposed of as Consuttthe user manual domestic waste A on the user manual y The product must be dispose of as electronic waste not as domestic waste Label Label ee ei iii did recycling of electrical and electronic equipment Label situated close to the laser aperture nn Label of laser warning placed on the back side of the machine Wavelength 810nm Max emission power 500mW Invisible laser radiation Avoid direct exposure to beam Class 3B laser STOP label for Emergency Warning laser beam label placed on the back of the machine MNPG127 01 Pag 15 MEDICAL DIVISION Appendix C ELECTRO MAGNETIC COMPATIBILITY TABLES Guidance and manufacturer s declaration electromagnetic emissions FOR ALL ME EQUIPMENT The ME EQUIPMENT is intended for use in the electromagnetic environment specified below The customer or the user of the ME EQUIPMENT should assure that it is used in such an
7. the maximum output power rating of the transmitter in watts W according to where P is the maximum output power rating of the transmitter in watts W according to the the transmitter manufacturer i transmitter manufacturer and d is the recommended separation distance in metres m Field 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 from structures objects and people Radiated RF IEC 61000 4 3 strengths from fixed RF transmitters as determined by an electromagnetic site survey 1 should be less than the compliance level in each frequency range 2 Interference may occur in the vicinity of equipment marked with the following symbol A NOTE 1 At 80 MHz and 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 1 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 loca
8. the probe laser cable to the proper plug placed on the front of the machine STARTING After the machine has been placed and installed using the instructions given in the previous chapters plug the power cable into the wall socket 230 Vac and switch on the device moving the key button on the ON position witch is placed on the front of the machine This operation prepares I TECH LA500 for use determining the switching on of the LCD display that shows that the equipment is ready to operate The default program is pre setted on CONTINUOS mode and the treatment time last 3 minutes Select the operation mode CONTINUOS or CYCLE using the buttons on the right side of the front panel picture below ge i en vag Coat BG With CYCLE mode it is possible to select the ON time from 1 to 9 seconds and the OFF time from 1 to 9 seconds using the buttons on the right side of the front panel next two pictures Enen BE ge 0200030 PE pr paz LE ge ng Select the treatment time using the TIME and TIME buttons placed on the left side of the front panel of the machine picture below You can select the treatment time from 30 seconds to 30 minutes You can set treatment intensity with the POWER e POWER buttons placed on the left side of the front panel The default power is setted to 200mW and the range is adjustable from 10mW to 500mW in according to treatment needs GG 0500
9. ACER srl service centre Some controls on the front control panel do not work properly Faulty keys or buttons Contact IACER srl service centre Control electronic circuit failure The device does not emit the therapy Parameters are not setted Check that the parameters have been correctly setted correctly Laser sources not working or Check laser source emission mode depleted Faulty components in the control electronic circuit Faulty supply of laser sources Contact IACER srl assistance centre The unit works properly but with a significant decrease in efficiency of the treatment Faulty or depleted laser source Possible break down in power generator circuit of the unit Contact IACER srl assistance centre The equipment starts up or seems to work properly but there is no emission No safety key or the interlock circuit is open Insert the DIN safety key into the front socket Reset the safety conditions not work Fuse s is are defective or Replace missing defective or interrupted interrupted fuse s Th electric circuit i Eon eee Contact IACER srl service centre broken MNPG127 01 Pag 13 E MEDICAL DIVISION TECHNICAL FEATURES Power supply 230 Vac 50 60 Hz 10 Diode probe Configuration of the laser probe Defocused Connection specific for the device Adjustabl
10. MEDICAL DIVISION LASER THERAPY LA MEDICAL DIVISION INDEX USER MANUAL 55 4 4 WRITING CONVENTIONS camara ee 4 WARRANTY GeBeBeReB RER TBER FREE SPEFBERPEFEFREEFBEBEDFEERERFBEREFEEFBOBESPEPBEEFEPBERPEERTEEDEBPDERFEPBERPEERFPER 4 oc cececsssenenavertarscececersenteavertetsteeees 5 CAUTIONS een aa era anna dass cease ceqeanaudesesavsessuceqeenaudesesecsessneeqeenananaeseses 5 SA A a o IIA 6 INTRODUCTION OF THE TECNOLOGY nun 7 The evolution of light nennen 7 The advantages of Laser therapy nenn 7 INTENDED USE 0000 une 8 INDICA HON airna E ee en 8 CONTRA INDICATIONS csssssecccccceeceesecccceeesaeeseeccceeeeseaeeaseeceeeeeseuaaseeeeesseagseeees 8 DEVICE DESCRIPTION Saa 9 PATIENTS PREPARATION e caccctcceunnsuiasnicscot sous aver vetnasuecscareouceuensenevsvavveresuceuensenassecsscts 9 HOW TO USE Mirra Os 9 MAINTENANCE iccccscacesnnsenannsansessassesnnanhanunanaeasehsaabessiasnsasanaash saahaaahasnhabunaaubaaasssanase 12 PANDE S CLEANING een 12 WORKING PROBLEM ssssesssesssssssssescsseososessssosseosososesssssscsososessssssssosososessssssosoe 12 ELECTROMAGNETIC INTERFERENCES nassen 13 TROUBLESHOOTING CHART Tiana Raso 13 TECHNICAL FEATURES a En En aa na nen ee een ats seen 14 APRENDICES si 15 Appendix A ENVIROMENTAL PROTECTION oooocccccnncncnnnonoccnnnnncnonananinocnnnnncnnnanonos 15 Appendix B LABELS sarao narnia coa 15 Appendix C ELECTRO MAGNETIC COMPATIBILITY TABLES eeeeeeee
11. e treatment time 0 30 minutes Diameter of the spot on the skin of lt 10 mm the patient Dimensions Length Height Depth 30x15x12 cm Weight main body 5 2 Kg temperature environment 5 40 C Conditions of use l relative humidity lt 80 without condensation temperature environment 5 40 C Storage transport conditions relative humidity lt 93 without condensation Atmospheric pressure 500 1060 hPa Maximum absorbed power 20 VA Double protection fuse on power 1 5 A T 5X20 mm supply T LCD display Icons Maximum Power 500 mW 20 Laser diode wavelength 810 nm Laser classification 3B DNRO m 2 3 Divergence 260 mrad Impulse duration set Emission CONTINUOUS Adjustable percentage of emitted power 0 100 Emission frequency set Pulsed mode ON OFF sec Pointing led Red light Classification in compliance with the directive 93 42 CEE IIB Output channels 1 Class of isolation parts applied according to the rule EN 60601 1 I BF Protection level against the liquids penetrations according to the BNO rule EN 60601 1 Button Command of execution of the treatment MNPG127 01 Pag 14 MEDICAL DIVISION APPENDICES Appendix B LABELS Anpenti A ENVIROMENTAL PROTECTION symbol The devices I TECH LA500 were designed and engineered to have minimal
12. eeeeeeeeeeeees 16 MEDICAL DIVISION USER MANUAL This manual is addressed to machine user owner Managers handling personnel installers users maintenance personnel It contains general information on the operation precautionary practices and maintenance information of the device I TECH LA500 This is an essential reference guide for users It is essential to read the manual carefully before installing and using the device and to keep it at hand for quick reference The manufacturer declines all responsibility for improper use of the machine use contrary to specific national laws incorrect installation defective power supply improper maintenance unauthorised modifications and interventions use of material or spare parts that are not specific for the model partial or complete non observance of the instructions supplied exceptional events To get further information consult the fabricant WRITING CONVENTIONS Certain sections of the manual have been underlined in order to highlight their importance NOTE These contain important information and useful tips for operating the equipment CAUTIONS The CAUTION message appears before operations which if not correctly performed may cause damage to the machine and or its accessories WARNING This signals operations or situations which if unknown to the operator or incorrectly carried out may harm the ope
13. er on a primary lesion or secondary non diagnosed Laser treatment may be granted to relieve pain during the terminal stage of disease it is recommended that this be performed only with the full consent of the patient thyroid the laser should not be used in any case above the gland bleeding vasodilatation may worsen the bleeding immuno suppressive therapy laser therapy is contraindicated in patients who have undergone such type of drug therapy inthe skin and injuries suspects never laser radiation on angiomas black points or injuries suspects on the skin treatments over the sympathetic ganglia the vagus nerve and region of the heart in patients with heart disease laser therapy can significantly alter the function neural and is therefore contraindicated in this regions body patients with heart disease Other Atopic dermatitis and eczema in the acute phase Inflammatory processes in place at the site to be treated Abrasions or bruises Photoallergy Recent surgery or cryotherapy in cutaneous sites to treat WARNING Photosensitivity reactions in some patients taking drugs known the latter are due to reactions of photosensitization It is not clear how the combination of laser and drugs triggers this response It is recommended that patients at risk allergic or patients with a history of such reactions are tested with a minimum time of treatment Means of fixation m
14. etal plates plastic NOT constitute contraindication to the use of lasers which can be safely used on metallic implants sutures and plastics MNPG127 01 Pag 8 1 TECK MEDICAL DIVISION DEVICE DESCRIPTION Remote interlock connector SS Aiii Radiator area Electric sockel 230 Emergency switch Radiator area Protection Fuse Power setup Time setup Probe socket Key switch Discontinuity time setup Wait Standby ContiuneCyclelcontinuity discontinuity Probe Electric power cable Protective glasses Wear before operations PATIENTS PREPARATION Before applying the laser therapy is necessary to prepare the skin of the patient This will allow to the laser light to reach better the zones to be treated and to reduce the risk of skin irritation For preparing the skin of the patient for the therapy carry out the following operations 1 wash the skin using soap and mild soap or alcohol where the head of the laser will be positioned 2 dry well the skin HOW TO USE IT CONNECTORS On the back of the machine is placed the power plug which is composed of the main plug for the power supply cable and the fuse holder with two fuses check technical information Insert the cable in the power plug check if the cable is correctly plug in the power plug MNPG127 01 Pag 9 1 TECK MEDICAL DIVISION Connect the interlock to the plug placed on the back of the machine Connect
15. fied to the use of the equipment in order to guarantee safety conditions to the patient Such equipment can be used in hospital environment outpatient nevertheless it is important to know that the user follows the medical instructions to use the equipment or that he follows the indications present in the user s manual INDICATIONS The application fields that can profit from using the laser therapy I TECH LA500 are the following 1 Arthro rheumatic pathology Arthrosis sciatica scapular and humeral periarthritis arthropathy of hands and feet epicondylitis hip arthrosis at its initial stage gonalgia with or without effusion myogenic stiff neck lumbago myositis chronic and acute pathologies etc 2 Rehabilitative therapy Articular motor rehabilitation after removing plaster apparatuses or after orthopaedic surgical operations 3 General medicine and dermatology Decubitus ulcers cheloids torpid sores for its well known bio stimulating and anti infectious effects CONTRA INDICATIONS direct radiation in the eye the human eye is extremely sensitive to laser radiation and can be permanently damaged from direct or reflected laser beams The special safety glasses must be worn by both patient by the operator pregnancy the laser is contraindicated for use over the pregnant uterus It can still be used in pregnant women with the foresight to not radiate over the abdomen neoplasms you must not use the las
16. gt 95 dip in UT for 0 5 cycles 70 UT 30 dip in 70 UT UT for 25 cycles lt 5 Uy per 0 5 cicli lt 5 UT for 0 5 cycles for 25 lt 5 UT gt 95 dip in UT for 5 sec lt 5 UT for 5 sec A IEC 60601 i Electromagnetic environment Immunity test Compliance level Test level guidance Floors should be wood concrete or ceramic tile If floors are covered with synthetic material the relative humidity should be at least 30 Mains power quality should be that of a typical commercial or hospital environment Mains power quality should be that of a typical commercial or hospital environment Mains power quality should be that of a typical commercial or hospital environment If the user of the ME EQUIPMENT requires continued operation during power mains interruptions it is recommended that the ME EQUIPMENT be powered from an uninterruptible power supply or a battery Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment NOTE UT isthe a c mains voltage prior to application of the test level MNPG127 01 Pag 16 O MEDICAL DIVISION Guidance and MANUFACTURER S declaration electromagnetic IMMUNITY Recommended separation distances between portable and mobile RF communications equipment FOR ME EQUIPMENT THAT ARE NOT LIFE SUPPORTING and the ME EQUIPMENT The ME EQUIPMENT is intended for use in t
17. hat allows ways to start up the machine is connected Because of security reasons the only specific software must be loaded into each machine In case of exchange of software the machine may immediately stop all its functions requiring the intervention of 1 A C E R srl technical assistance MNPG127 01 Pag 5 MEDICAL DIVISION USE WARNINGS The perfect functionality of the device is guaranteed in accordance with the rules of installation and of use included only with original accessories and spare parts If there are problems or installation difficulties please contact the A C E R srl technical assistance department The correct position while moving the machine the apparatus has to be moved exclusively by gripping it with both hands on the curved profiles of the lid If you want to install an extern interlock circuit contact exclusively qualified technicians and supply them the scheme correspondent to the room used for the emission of the treatment A bad installation of the device can to generate serious ocular lesions Before connecting the cable to the mains plug check that the equipment wasn t damaged during transport Ensure that the power supply specifications on the mains socket correspond with the information on the label attached to the back of the unit The electric current that powers the unit is VERY DANGEROUS Before connecting or disconnecting the power cable from the connecter on the unit
18. he electromagnetic environment specified below The ME EQUIPMENT is intended for use in an electromagnetic environment in which radiated RF The customer or the user of the ME EQUIPMENT should assure that it is used in such an disturbances are controlled environment The customer or the user of the ME EQUIPMENT can help prevent electromagnetic interference by IEC 60601 Test Electromagnetic maintaining a minimum distance between portable and mobile RF communications equipment Immunity test Compliance level i level environment guidance transmitters and the ME EQUIPMENT as recommended below according to the maximum output Portable and mobile RF communications equipment should be used no closer to any part of power of the communications equipment the ME EQUIPMENT including cables than the recommended separation distance calculated Distanza di separazione alla frequenza del trasmettitore m from the equation applicable to the frequency of the transmitter 150 kHz 80 MHz 80 MHz 800 MHz 800 MHz 2 5 GHz Recommended Rated maximum output separation distance power of transmitter W Conducted RF 3V IEC 61000 4 6 da 150kHz a 80MHz Er from 80 to E m 800MH from 80MHz to 3V m E 2 5GHz d 7 JP from 800MHz For transmitters rated at a maximum output power not listed above the recommended separation E distance d in metres m can be determined using the equation applicable to the frequency of the to 2 5GHz transmitter where P is
19. make sure it is plugged out from the mains socket The power cable has an earthed plug for safety reasons Only use with a mains socket suitable for use with earthed systems The equipment should only be connected to electrical systems that fully comply with regulations Check the integrity and the existence of ground conductor if extensions cables are used Connect the equipment directly to the wall socket without using extensions Failure to comply with these warnings may result in dangerous electrical discharges that could cause injury operators and compromise the functioning of the unit The laser therapy treatments must be provided under the strict control of the operator patients conscious able to interact with the operator in response to stresses transmitted by the device in case of default to the indications given A C E R srl shall not be consider responsible for any accidents The use of the controls or regulations or the execution of different procedures from those specified in this user manual can cause the exposition to dangerous radiation The operator has the responsibility to verify that the issuing head remains well in contact to the zone of treatment to avoid the emission to different zones from those to be treated The laser radiation that outgoings from the device is dangerous always use the appropriate glasses Always avoid the exposition of the eyes to the direct or reflected laser beam It is recom
20. mended not to start treatment if the machine is not in perfect mechanical condition or if the laser does not present characteristics of approved for this purpose see the specifications table During the delivery the handpiece must be positioned in contact with the part to be treated After activating the handpiece through the pedal contact avoid that it moves or is directed to different areas THE PROBE MUST NEVER BE DIRECTED TO AREAS OF BODY SENSITIVE TO THE LASER RADIATION FOR EXAMPLE THE EYES ALWAYS AVOID THE EXPOSITION OF THE EYE TO THE DIRECT OR REFLECTED LASER BEAM Do not leave the device switched on unattended always switch off after use Use only probes accurately cleaned and disinfected after each treatment in order to avoid environment and users contamination The operator must pay attention to the necessity of a periodic maintenance every 2 years of the probes applicators IACER srl authorised personnel should carry out such operations It is absolutely forbidden in presence of anaesthetic inflammable substances and in full oxygen environment 1 A C E R will be not responsible if these indications will be not complied It is absolutely forbidden to cover the ventilation slots such an action may not allow the machine to work in safe conditions In case of non compliance with this indication A C E R Srl will not be responsible for any accidents It s important to pay the attention of the operator to the necessity to verify
21. ot use chemical solvents or abrasive detergents If you need any kind of information about the original accessories and spare parts please contact contact the manufacturer Don t sprinkle and spill any kind of liquid into the case or into the air slots placed on back of I TECH LA500 Please don t immerse the device into the water After the cleaning of the box please dry correctly all the accessories and other parts before start a new treatment It is absolutely forbidden disassemble the device for cleaning or for checking inside there is no reason for cleaning the inside of the machine I TECH LA500 and in any case this operation must be done only by authorized 1 A C E R technicians WORKING PROBLEM In case of working problems we recommend to consult the table at the paragraph TROUBLESHOOTING CHART before contacting the manufacturer Unplug the device from power socket and contact the manufactures in the following situations e The power cable or the plug placed on the back side of the machine are broken or damaged e A liquid is penetrated into the device e The device has been exposed to the rain MNPG127 01 Pag 12 MEDICAL DIVISION ELECTROMAGNETIC INTERFERENCES The I TECH LA500 equipment has been designed and manufactured according to the ELECTROMAGNETIC COMPATIBILITY DIRECTIVE 2004 108 CE with the aim of providing adequate protection from harmful interference when installed in homes and health establishmen
22. rator WARRANTY IACER srl guarantees the quality of its products for a period of 24 months from the date of purchase when information contained in this manual regarding installation use and maintenance is strictly adhered For professional user warranty is for a period of 12 months from the date of purchase During the warranty period the faulty parts will be replaced or repaired according to company discretion The warranty does not however include the replacement of the equipment The warranty does not cover damages resulting from incorrect connection and installation incorrect use due to non compliance with instructions contained in this manual improper or inadequate maintenance use of the machine in environmental conditions which do not conform with those specified for the product unauthorized opening of the outer casing tampering or unauthorized modifications MNPG127 01 Pag 4 MEDICAL DIVISION use of non original accessories The warranty is supplied ex works Should you need to return the goods then please note the packing instructions as follows Enclose a copy of the purchasing receipt Before sending the machine back for suspected malfunction we recommend that first you carefully consult sections regarding MAINTENANCE and TROUBLESHOOTING of the manual as a large part of the problems and faults are usually due to inadequate maintenance or small technical problems which can often be ea
23. rovided they might damage the unit causing the warranty to become void In case you have any problems or difficulties with installation contact 1 A C E R srl technical support If using the same extension for the unit and other units make sure that the total current being absorbed by the connected units does not exceed the max current allowed for that type of cable and that however it does not exceed 15 A The protocols of therapeutic suggestion preloaded on the machine cannot be deleted Itis not possible to define a number of sessions suggested to evaluate the effectiveness of the treatment since they are related to the power delivered to the patient undergoing treatment It is task of the physician to decide the number of therapy sessions which subject the patient according to the specific requirements of the case in order to ensure to the patient himself the execution of an effective treatment in time and place in conditions of absolute safety Always control sometimes the integrity of the cable and of the probe applicator connector they must not be damaged or worn USE The laser radiation that outgoings from the device is dangerous always use the appropriate glasses always avoid the exposition of the eyes to the direct or reflected laser beam Before beginning any treatment both operator and patient must wear the PROTECTIVE GLASSES Before switching the device on be sure that the INTERLOCK key t
24. sily solved by the user himself When re packing the equipment for return to the manufacturer proceed as follows 1 unplug the machine and any connections devices applicators etc 2 carefully clean and disinfect all parts of the machine and accessories which have been in contact with patients Any equipment which the technical department does not consider hygienic Italian law T U S 81 2008 on safety in the workplace will not be accepted 3 disassemble accessories and any mechanical supports 4 use original box and packing materials 5 Enclose detailed information regarding the nature of the problem in order to facilitate the technical department s intervention and save time on repair NOTES PRELIMINARY NOTES The installation of the device does not require any special care is therefore simple and immediate MAINTENANCE For an optimal use of the device and to guarantee its maximum performance it is recommended to perform maintenance at the correct time and suggested CAUTIONS PRELIMINARY NOTES The customer is liable for all damage caused by inadequate packaging of the material Keep the original packaging of the unit it will be needed if the unit is returned to the company Do not use the equipment in places where it might get wet Before operating the machine carefully check the correctness of the connections according to the instructions Do not use accessories other than the ones p
25. the laser light is supplied in the right quantities you will obtain a stimulation of certain cellular functions especially in the presence of cells with functional deficiencies The biological action in using the Laser therapy produces a series of effects on the cells in function of a stimulating action on mitochondrial functions with a higher production of ATP The applications of the I TECH LA500 laser produce a number of effects on the treated tissues 1 increase in hematic flow vasodilatation of capillaries and arteries 2 biostimulation tissue regeneration stimulation of the protein synthesis stimulation of the production of ATP stimulation of the fibroblast mitosis increase in collagen and elastin 3 anti inflammatory effect 4 anti edematous effect with stimulation of the lymphatic system 5 analgesic effect increase in the perception threshold of nerve endings I TECH LA5OO is therefore a laser with the following characteristics thanks to the power adjustable up to 500mW and to the 810 nm wavelength it allows the stimulation of the deepest layers of the treated tissue thus favoring a rapid and diffused cellular re generation with I TECH LA500 it is possible to obtain a deep tissue stimulation and this makes possible to treat the most internal tissues and structures such as the femoral joint and chronic pathologies such as arthrosis it may be used in many fields such as sports medicine orthopedics
26. tion in which the ME EQUIPMENT is used exceeds the applicable RF compliance level above the ME EQUIPMENT should be observed to verify normal operation If abnormal performance is observed additional measures may be necessary such as re orienting or relocating the ME EQUIPMENT 2 Over the frequency range 150 kHz to 80 MHz field strengths should be less than V1 V m MNPG127 01 Pag 17 TEGH MEDICAL DIVISION Head office and warehouse 30030 MARTELLAGO VE Via S Pertini 24 A Tel 0039 041 5401356 Fax 0039 041 5402684 Cod Fisc P IVA IT 00185480274 R E A VE N 120250 M VEOO1767 e mail iacer iacer it Internet www itechmedicaldivision com
27. ts The I TECH AR equipment does not generate significant radio frequency energy and is adequately immune to radiated electromagnetic fields Therefore it does not detrimentally interfere with radio electric communications electro medical equipment for monitoring diagnosis therapy and surgery office electronic devices such as computers printers photocopiers fax machines etc or any electric or electronic equipment used in these environments as long as said equipment complies with the ELECTROMAGNETIC COMPATIBILITY directive In any case in order to avoid any interference problems we recommend that you operate the therapy equipment far enough away from critical equipment for monitoring vital patient functions and that you be careful when applying therapy to patients with pacemakers TROUBLESHOOTING CHART PROBLEM POSSIBLECAUSE SOLUTION The power plug is inserted not correctly in the socket The power cable is not inserted correctly into the connector of the Check that the socket works properly Insert correctly the plug and the cable The LCD display in in the connector of the device device the frontal panel The power cable is worn out or does not turn on Replace the power cable interrupted the device does The emergency switch is off Turn on the emegency switch The LCD display in the frontal panel does not turn on Defective components in the control electric board Contact I
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