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1. ON OFF button EM COMPATIBILITY EMC TABLES Polarity of power supply Stop treatment Start Pause button Protected against the effects of immersion for ultrasound handle WEE Regulations 3 658 Applied part type BF Use the I TECH UE device at least 3 metres away from televisions monitors mobile phones WIFI routers or any other electronic device as they may affect its functioning The device must be installed and commissioned in compliance with the information on electromagnetic compatibility supplied in this manual Also see the EMC Charts paragraph Using accessories transducers and cables other than those specified except for those transducers and cables sold by the manufacturer as spare parts for internal components may result in increased emissions or decreased immunity of the device The device should not be placed next to or on top of other devices Should it prove necessary to place it next to or on top of other devices supervision is essential at all times to control its normal functioning rN P Product in compliance with Directive 93 42 EEC MDD Guidance and manufacturer s declaration electromagnetic emissions FOR ALL EM DEVICES Device can supply a current 10mA r m s or 10V r m s for a period of 5 seconds The I TECH UE device is intended for use in the electromagnetic environment specified below The customer or the user of the I T
2. 30 EM COMPATIBILITY EMC TABLES 30 WARRANTY g P 32 I TE 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 UE 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 Partial or complete non observance of the recommendations may lead to malfunction and damage of the device and therefore the warranty will no longer be valid Following the provisions and the recommendations supplied by the manufacturer scrupulously is the only way of achieving the best results and to benefit from a quick and efficient technical assistance if needed The limits of this manual the user manual cannot replace actual user experience for particularly demanding operations this instruction manual only represents a remainder of the main operations This user manual must be considered an integral part of the equipment and must be preserved for future reference until the device is dismantled The instruction manual must be available for reference at the place of use of the device and pres
3. 3 2 CC 10Hz 180ps 0 min 3 CC 10Hz 180ps 10 min 1 CC 80Hz 100 30 min EMS 4 2 CC 80Hz 100ps 0 min 3 CC 80Hz 100ps O min 1 CC 180Hz 30us 16 min 5 2 CC 180Hz 30us 0 min 3 CC 180Hz 30us 0 min 1 CC 120Hz 70us 14 min 6 2 CC 120Hz 70us 14 min 3 120Hz 70us 14 min 1 CC 120Hz 70us 14 min 7 2 CC 120Hz 70us 14 min 3 CC 120Hz 70us 14 min 1 CC 120Hz 70us 14 min 8 2 CC 120Hz 70us 14 min 3 CC 120Hz 70us 14 min 1 CC 120Hz 70us 14 min 9 2 CC 120Hz 70us 14 min 3 CC 120Hz 70us 14 min 1 CC 120Hz 70us 14 min 10 2 CC 120Hz 70us 14 min 3 CC 120Hz 70us 14 min I A C E R Srl 23 Waveform PRG Phase CC CV Carrier frequency C F Freq Duty cycle Contraction Ramp Time Recovery 1 CC 2 5kHz 50Hz 50 10s 10s 1s 10 min 1 2 CC 2 5kHz 50Hz 50 10s 10s 1s 0 min 3 CC 2 5kHz 50Hz 50 10s 10s 1s 0 min 1 2 5kHz 50Hz 5096 4s 12s 1s 10 min 2 2 CC 2 5kHz 50Hz 50 4s 12s 1s 0 min 3 cc 2 5kHz 50Hz 50 4s 12s 1s 0 min 1 cc 2 5kHz 50Hz 50 4s 12s 1s 10 min 3 2 CC 2 5kHz 50Hz 50 4s 12s 1s 0 min 3 CC 2 5kHz 50Hz 50 4s 12s 1s 0 min 1 2 5kHz 50Hz 50 10s 10s 1s 30 min 4 2 CC 2 5kHz 50Hz 50 10s 10s 1s 0 min 3 2 5kHz 50Hz 5096 105 105 15 Russian 1 CE 2 5kHz 50Hz 5096 55 55 1s 20 min 5 2 2 5kHz 50Hz 5096 5s 5s 1s 0 min 3 2 5kHz 50Hz 5096 5s 5s 1s 0 min
4. 8 Ultrasound Intensity selection knob 9 Power supply socket 10 button 11 Handle socket 12 Electrostimulation cable socket I A C E R Srl I TEGE MEDICAL DIVISION LEGEND CC Constant current output mode CV Constant voltage output mode F M Frequency modulation Burst Burst frequency Freq Frequency C F Carrier frequency Duty Duty cycle for Russian waveform Kotz for B5 button Beat H High beat frequency selection A M Amplitude modulation Beat L Low beat frequency selection P Dur Impulse duration Treat Therapy time Cycle Contraction recovery cycle Ramp Ramp time Duty Duty cycle for ultrasound for B8 button Freq Ultrasound frequency INTERFACCIA I A C E R Srl IF 4P IF 2P saj HH DY TENS 588 5882 LABELS MODEL ELECTRICAL ST Output intensity 0 100mA 1000 ohm load Frequency 1 250Hz Beat frequency 1 150Hz Power supply DCISV 3 0A Adaptor LA C E RSrlvia S Pertini 24 A 30030 Martellago V E HITALY T CH SN 000001 I TECH UE ULTRASOUND Waveform Pulsed Acoustic Frequency L0MHz 10 1 OM Hz 105 Modulation wave shape 100Hz 10 Duty factor 10 100 le 3 0W em R Max 8 0 Beam type collimated IMULATION tJ A O T 5 0cm t20 1 MHz 3MHz P 15 0W 20 7 0cm Ry Max 5 0 IPX7 Beam type coll
5. experience undesired reactions such as hot flushes in the treated area Check the treated area before during and after the treatment and suspend it in case of undesired effects Make sure that the handpiece is in contact with the skin using a specific ultrasound gel Any substance used for this purpose must be highly conductive Air is a terrible conductor of ultrasound waves USE I TECH UE is a device for ultrasound therapy Ultrasound treatment is indicated for several chronic and sub chronic treatments as I A C E R Srl Muscle pains and contractures Contractures Capsulitis Bursitis Myositis I TECH e Softtissues diseases e Tendinitis Tendinosis Electrotherapy TENS interferential waves premodulated EMS and Kotz Russian is particularly indicated for the treatment of chronic and acute pains for post operated oedema and in presence of inflammations Electrotherapy is also indicated for rehabilitation post trauma and for the prevention of muscle atrophy Moreover it is indicated for local circulation increase and for muscle maintaining Use hospital and domestic use it is recommended the use only by seasoned professional Expected lifetime time after which we suggest sending the device to the manufacturer for safety checks 2 years I A C E R Srl I TECH CONDITIONS OF USE and EQUIPMENT 9 Environmental conditions for use Environment temperature from
6. 1 cc 2 5kHz 50Hz 50 10s 10s 1s 10 min 6 2 cc 2 5kHz 50Hz 50 10s 10s 1s 10 min 3 cc 2 5kHz 50Hz 50 10s 10s 1s 10 min 1 cc 2 5kHz 50Hz 50 10s 10s 1s 10 min 7 2 cc 2 5kHz 50Hz 50 10s 10s 1s 10 min 3 cc 2 5kHz 50Hz 50 10s 10s 1s 10 min 1 CC 2 5kHz 50Hz 50 10s 10s 1s 10 min 8 2 2 5kHz 50Hz 5096 10s 10s 1s 10 min 3 cc 2 5kHz 50Hz 50 10s 10s 1s 10 min 1 cc 2 5kHz 50Hz 50 10s 10s 1s 10 min 9 2 cc 2 5kHz 50Hz 50 10s 10s 1s 10 min 3 cc 2 5kHz 50Hz 50 10s 10s 1s 10 min 1 cc 2 5kHz 50Hz 50 10s 10s 1s 10 min 10 2 cc 2 5kHz 50Hz 50 10s 10s 1s 10 min 3 cc 2 5kHz 50Hz 50 10s 10s 1s 10 min I A C E R Srl 24 ie HE Nut COMBINED TREATMENT ULTRASOUND ELECTROTHERAPY Follow the indications below to start the combined treatment 1 10 11 In combo mode ultrasound probe works as negative of channel 2 you should connect electrotherapy cable with 1 derivation red cable to the green cable on the output 2 The channel 1 is turned off Connect the green cable to the socket 12 placed on the back side of the device Connect the electrode to the red cable for electrotherapy Place the electrode on the treatment area following the instruction of the previous paragraphs The electrode should be placed near the painful zone approximately 10 15 cm far from the painful poin
7. 10 to 40 C Relative humidity from 10 to 93 without condensation avoid direct sunlight chemical products and vibrations The device is equipped with the following accessories Description Silicone conductive electrode 70x110mm Sponge for silicone electrode 80x120mm Elastic belt for electrodes fastening 75x1200mm Electrical stimulation cables with 2 derivations red black Electrotherapy cable Ultrasound head with 5cmq area Electrodes positions user manual Ultrasound gel 2 pieces 2 pieces 2 pieces 1 piece 9 2 2 w os j All accessories are available on demand as spare parts Moreover the multi frequency 1 3 MHz ultrasound head with 1 cmq area is available on demand I A C E R Srl 7 I TECH DEVICE DESCRIPTION Channel 1 intensity selection knob Channel 2 intensity selection knob Programs parameters control knob and PAUSE Parameter confirm and STOP button Led indicator LCD display Parameters selection buttons TS te B1 mode selection ultrasound electrotherapy combined and waveform selection B2 program selection B3 Burst vector frequency modulation selection B4 frequency carrier frequency selection B5 Duty cycle high frequency width modulation selection B6 low frequency impulse duration selection B7 therapy time contraction recovery cycle ramp up selection B8 frequency ultrasound duty cycle selection
8. 2 5kHz 110Hz 100Hz 15 min 10 2 CC 2 5kHz 110Hz 100Hz 15 min 3 CC 2 5kHz 110Hz 100Hz 15 min I A C E R Srl 21 Waveform PRG Phase CC CV Freq Width impulse P Dur Time 1 CC 120Hz 70us 14 min 1 2 CC 120Hz 70us 0 min 3 120Hz 70ys 0 min 1 CC 200Hz 60us 20 min 2 2 CC 200Hz 60us 0 min 3 200 7 60us 0 min 1 CC 10Hz 180ps 20 min 3 2 CC 10Hz 180ps 0 min 3 CC 10Hz 180ps 10 min 1 CC 80Hz 100 30 min 4 2 CC 80Hz 100ps 0 min 3 CC 80Hz 100ps O min 1 CC 180Hz 30us 16 min 5 2 CC 180Hz 30us 0 min 3 CC 180Hz 30us 0 min 1 CC 120Hz 70us 14 min 6 2 CC 120Hz 70us 14 min 3 120Hz 70us 14 min 1 CC 120Hz 70us 14 min 7 2 CC 120Hz 70us 14 min 3 CC 120Hz 70us 14 min 1 CC 120Hz 70us 14 min 8 2 CC 120Hz 70us 14 min 3 CC 120Hz 70us 14 min 1 CC 120Hz 70us 14 min 9 2 CC 120Hz 70us 14 min 3 CC 120Hz 70us 14 min 1 CC 120Hz 70us 14 min 10 2 CC 120Hz 70us 14 min 3 CC 120Hz 70us 14 min I A C E R Srl 22 Waveform PRG Phase CC CV Freq Width impulse P Dur Time 1 CC 120Hz 70us 14 min 1 2 CC 120Hz 70us 0 min 3 120Hz 70ys 0 min 1 CC 200Hz 60us 20 min 2 2 CC 200Hz 60us 0 min 3 200 7 60us 0 min 1 CC 10Hz 180ps 20 min
9. according to electrodes positions user manual The distance between the electrodes should be at least of 5 cm 1 MEDICAL DIVISION devices are designed and manufactured to have minimum negative impact on the environment in compliance with the functioning and safety needs We follow the criteria to minimise waste toxic material noise undesired radiations and energy consumption I A C E R Srl 27 Ea L m ewe A careful research on the performance of the device guarantees a significant reduction of consumption in line with the concept of energy saving This symbol indicates that the product must not be disposed of with normal domestic waste Please dispose of the device in accordance with the directive 2002 96 EC WEEE Waste Electrical and Electronic Equipment TECHNICAL FEATURES Caratteristiche generali Power supply Input 100V 240V 47Hz 63Hz 1 35A Output 15VDC 3A max Dimensions 143mmx73mmx40mm Device Dimensions 250mmx185mmx82mm Environmental conditions for use Temperature from 10 C to 40 C Relative humidity 10 93 Environmental conditions for storage Temperature from 20 C to 55 C Relative humidity 20 90 Maximum adjustable therapy time 60 minutes for electrotherapy Timer accuracy 3 Classification EN 60601 1 Class Applied part Type BF Ultrasound features Ultrasoun
10. cable to the power supply Connect the power supply to the device connector Connect the power supply plug to the wall socket Press on ON OFF button to switch on the device ULTRASOUND TREATMENT Follow the instructions below for ultrasound treatment 1 Connect the ultrasound handle to the socket 11 placed on back side of the device Connect the cable when the device is switched off Switch on the device pressing ON OFF button placed on lateral side next to power supply plug Immediately after switching on the device carries out a self test 10 seconds duration At the end display shows the last percome treatment ce Press WAVEFORM MODE B1 button to show icon this icon indicates ULTRASOUND treatment Press B8 button to regulate ultrasound working frequency 1 or 3 MHz by using the knob 3 Press again B8 button to regulate the duty cycle it s possible to adjust the value from 10 to 100 stepping 10 using the knob 3 Srl 10 11 12 13 Press B7 button to regulate therapy time it s possible to adjust therapy time from 1 to 30 minutes stepping 1 minute by using the knob 3 Put a good quantity of conductive gel on the area to be treated or on ultrasound head It is recommended to use a CE conductive gel CE Regulate the treatment intensity using the knob 8 Press the knob to adjust unit of measurement W Watt or W cm Watt cmq Keep the head in constant con
11. or ceramic tile If floors are covered with synthetic material the relative humidity should be at least 30 96 part of the I TECH UE device including cables than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter 3v m Recommended separation Radiated RF IEC 61000 from goMHz 3V m E bet from 150kHz to 80MHz sa d 1 2 VP from 80 MHz to 800 MHz d 2 3 NP from 800 MHz to 2 5 GHz where P is the maximum output power rating of the transmitter In watts W according to the Guidance and manufacturer s declaration Electromagnetic immunity FOR EM DEVICES THAT ARE NOT INTENDED FOR LIFE SUPPORT The I TECH UE device is intended for use in the electromagnetic environment specified below The customer or the user of the I TECH UE should assure that it is used in such an environment Transmitter manufacturer and d Is the recommended separation distance in meters m Field strengths from fixed RF transmitters as determined by an electromagnetic site a survey should be less than the compliance level b in each frequency range Interference may occur q In the vicinity of equipment marked with the following NOTE At 80 MHz ends 800 MHz the higher frequency range applies Immunity test IEC 60601 test level Compliance level Electromagnetic environment guidance NOTE 2 These guidelines may n
12. smaller in surface area than 25cm self adhesive electrode ATTENTION Electrodes in contact with each other could result in improper stimulation or skin burns Output current density is related to electrode size Improper application may result in patient injury In case of doubts about the proper electrode size consult a doctor therapist specialized in electrostimulation Use only cables and electrodes recommended by the fabricant This device is supplied with 50mmx50mm 50mmx100mm adhesive electrodes You can select the correct adhesive electrodes according to treatment area and output current density It is recommended to use electrodes supplied by the fabricant to guarantee the highest level of contact with the area to be treated and the right current density in relation with the prescribed treatment Properly dispose of electrodes after the use In case of doubts about the electrodes integrity it is suggested to replace them by new ones Do not start the treatment before electrodes are correctly placed on the skin Do not take away the electrodes during the therapy Pregelled electrodes positioning Insert the cable with the Red connector into one adhesive electrode Insert the cable with the Black connector into one adhesive electrode Make sure that the connectors are inserted completely and there are no metal parts of the pins exposed Remove the adhesive electrodes from the protective backi
13. to confirm the value for each phase Select CONSTANT CURRENT CC or CONSTANTE VOLTAGE CV by pressing again PROGRAM CC CV m button The unity of measurement changes from mA LL Select the waveform features by pressing B3 B7 buttons each waveform has different technical features e select frequency modulation vector Burst B4 select frequency carrier frequency B5 select duty cycle high frequency width modulation B6 select low frequency impulse duration B7 select therapy time contraction recovery cycle slope milliAmpere to V Volts Press the button of the selected parameter and regulate the value by using the knob 3 Press FREQ DUTY B8 button and select the working frequency 1 or 3 MHz by using the knob 3 Press B8 button to regulate the duty cycle it s possible to select the value from 1096 to 10096 stepping of 10 by using the knob 3 Press B7 button to select therapy time it s possible to select therapy time from 1 to 30 minutes stepping of 1 by using the knob 3 25 HT r SION 17 Put a good quantity of conductive gel on the area to be treated It is recommended to use a CE conductive gel 18 Select electrotherapy intensity by using the knob 2 of the Channel 2 19 Select treatment intensity by using the knob 8 Press the knob to select the unity of measurement W Watt W cm Watt cmq 20 Keep the head in constant contact wit
14. 0 15 Cavitations U 01 10 Affected area 1MHz 7096 20 min 5 cmq 2W cm 3W cm 20 30 T T headache U 01 10 Cervical area 1MHz 5096 15 min 5 cmq 1 0W cm 1 5W cm 10 15 T T headache U 01 10 Massetere 1MHz 5096 15 min 5 cmq 1 5W cm 10 15 Cervicalgias U 01 10 Cervical area 1MHz 5006 15 min 5 cmq 1 0W cm 1 5W cm 10 15 Whiplash U 01 10 Cervical and dorsal 1MHz 5096 15 min 5 cmq 1 0W cm 1 5W cm 10 15 front zone Condropathy U 01 10 Affected area 1MHz 6096 15 min 5 cmq 1 0W cm 1 5W cm 10 15 Muscle contractures U 01 10 Affected area 1MHz 7096 20 min 5 cmq 2W cm 4 6 I A C E R Srl 13 Coxarthrosis U 01 10 Hip 1MHz 60 15 min 5 2W cm 10 15 Cramps U 01 10 Affected area 1MHz 7096 20min 5cmq 2W cm 4 6 Cruralgy U 01 10 Internal thigh 1MHz 4096 15 min 5 cmq 2W cm 10 15 Discopathy U 01 10 Affected area 1MHz 5096 15 min 5 cmq 1 0W cm 1 5W cm 10 15 Strains U 01 10 Affected area 1MHz 5096 15 min 5 cmq 1 0W cm 1 5W cm 10 15 Articular pain U 01 10 Affected area 1MHz 50 15 min 5 cmq 1 0W cm 1 5W cm 10 15 Intercostal pain U 01 10 Affected area 1MHz 50 15 min 5 cmq 1 0W cm 1 5W cm 10 15 Menstrual pain U 01 10 Abdomen 1MHz 50 15 min 5 cmq 1 0W cm 1 5W cm 10 15 Muscle pain U 01 10 Affected area 1MHz 50 15 min 5 cmq 1 0W cm 1 5W cm 10 15 Rheumatic pain U 01 10 Affected area 1MH
15. 6 Fax 0039 041 5402684 Cod Fisc P IVA IT 00185480274 R E A VE N 120250 M VE001767 e mail iacer iacer it Internet www itechmedicaldivision com
16. ECH UE should assures that it is used in such an environment Fabricant name and address Manufacturing date month year Emissions test Compliance Electromagnetic environment guidance The I TECH UE device uses RF energy only for its RF emissions Group 1 internal function Therefore its RF emissions are CISPR 11 very low and are not likely to cause any interference in nearby electronic equipment Attention Consult operating instructions RF emissions Class B CISPR11 The I TECH UE device is suitable for use in all Harmonic emissions N A establishments other than domestic and those IEC 61000 3 2 directly connected to the publiclow voltage r si E gt O Ultrasound handle lot powersupply network that supplies buildings Voltage fluctuations used for domestic purposes flicker emissions IEC 61000 3 3 A C E R Srl 30 Guidance and manufacturer s declaration electromagnetic Immunity The I TECH UE device is intended for use in the electromagnetic environment specified below The customer or the user of the I TECH UE should assure that it is used in such an environment Immunity test IEC 60601 test level Compliance level Electromagnetic environment guidance Electrostatic discharge ESD IEC 61000 4 2 36 kV contact 3 6kV contact 8kV air 8kV air Floors should be wood concrete
17. Free Indications regarding intensity and number of sessions can vary depending on the opinion of your personal doctor or therapist In particular indications on intensity do not consider the width of the area to be treated If it is very wide the intensity can be increased by 2096 with respect to what indicated and it can be reduced if it is a small area Similarly the movement on the area must be appropriate to the heat felt by the patient The slower it moves the stronger the heat If the patient complains about the heat we advise reducing the intensity or moving the head faster I A C E R Srl 16 I TECH PRELIMINARY ELECTROTHERAPY INSTRUCTIONS Before start treatment pay attention to the following indications Insure there are no contraindications to treatment Insure there are no abrasions or irritations in the area to be treated Clean the skin with neutral soap or alcohol 70 If the skin is hairy it is suggested to shave the area for an optimal treatment Test the heat sensibility of the treatment area Guarantee a good contact between electrodes and skin Check that electrodes are correctly placed on the skin during the treatment Examine the skin after the treatment Choose the electrodes dimensions taking into consideration the area to be treated Follow electrode manufacturer s instructions e To avoid skin irritation due to high current density do not use electrodes
18. Hz 110Hz 100Hz 15 min 3 CC 0 45 4 0kHz 110Hz 100Hz 15 min 1 CC 0 45 4 0kHz 110Hz 100Hz 15 min 9 2 CC 0 45 4 0kHz 110Hz 100Hz 15 min 3 CC 0 45 4 0kHz 110Hz 100Hz 15 min 1 CC 0 45 4 0kHz 110Hz 100Hz 15 min 10 2 CC 0 45 4 0kHz 110Hz 100Hz 15 min 3 CC 0 45 4 0kHz 110Hz 100Hz 15 min I A C E R Srl 20 Waveform PRG Phase CC CV Carrier frequency High frequency Beat H Low frequency Beat L Time C F 1 CC 2 5kHz 110Hz 100Hz 15 min 1 2 CC 2 5kHz 110Hz 100Hz 0 min 3 CC 2 5kHz 110Hz 100Hz 0 min 1 CC 2 5kHz 150Hz 100Hz 10 min Interferential2 2 2 CC 2 5kHz 150Hz 100Hz 0 min poles 3 CC 2 5kHz 150Hz 100Hz 0 min 1 CC 2 5kHz 50Hz 50Hz 15 min 3 2 CC 2 5kHz 50Hz 50Hz 0 min 3 CC 2 5kHz 50Hz 50Hz 10 min 1 CC 2 5kHz 150Hz 90Hz 15 min IF 2P 2 CC 2 5kHz 150Hz 90Hz 0 min 3 CC 2 5kHz 150Hz 90Hz 0 min 1 CC 2 5kHz 110Hz 100Hz 15 min 5 2 CC 2 5kHz 110Hz 100Hz 0 min 3 CC 2 5kHz 110Hz 100Hz 0 min 1 CC 2 5kHz 110Hz 100Hz 15 min 6 2 CC 2 5kHz 110Hz 100Hz 15 min 3 CC 2 5kHz 110Hz 100Hz 15 min 1 CC 2 5kHz 110Hz 100Hz 15 min 7 2 CC 2 5kHz 110Hz 100Hz 15 min 3 CC 2 5kHz 110Hz 100Hz 15 min 1 CC 2 5kHz 110Hz 100Hz 15 min 8 2 CC 2 5kHz 110Hz 100Hz 15 min 3 CC 2 5kHz 110Hz 100Hz 15 min 1 CC 2 5kHz 110Hz 100Hz 15 min 9 2 CC 2 5kHz 110Hz 100Hz 15 min 3 CC 2 5kHz 110Hz 100Hz 15 min 1 CC
19. I TECE MEDICAL DIVISION TECHUE MNPG118 Rev 0 03 08 2013 SUMMARY SUMMARY 2 USER MANUAL 3 SAFETY INFORMATION ccrccrrrrrrene rire se ne eee eee z arene aa nere n iena nice sana 3 USE 5 5 CONDITIONS OF USE and EQUIPMENT 7 DEVICE DESCRIPTION aaa 8 INSTALLATION 11 ULTRASOUND TREATMENT 11 PRELIMINARY ELECTROTHERAPY INSTRUCTIONS 17 ELECTROTHERAPY TREATMENT eee rece nana rene sanare nice sanitas 18 COMBINED TREATMENT ULTRASOUND ELECTROTHERAPY 25 CLEANING MAINTENANCE AND STORAGE 26 OPERATION TROUBLES eee eee nie nare cesena rene e eee eee narice seni zineenane 27 ENVIRONMENT PROTECTION 27 TECHNICAL rene ee rece eee nice ezine eee seni ene rice asit assa neas nau 28 USER MANUAL SYMBOLS
20. LE AND MOBILE RF COMMUNICATIONS EQUIPMENT AND THE EM DEVICES THAT ARE NOT INTENDED FOR LIFE SUPPORT The I TECH UE device is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled The customer or the user of the I TECH UE device can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment transmitters and the I TECH UE as recommended below according to the maximum output power of the communications equipment Separation distance according to frequency of transmitter m Rated maximum output From 150kHz to From 80MHz to From 800MHz to 2GHz power of transmitter W 80MHz d 1 2 JP 800MHzd 1 2 P 2 3 0 01 0 12 0 12 0 23 0 1 0 37 0 37 0 74 1 1 17 1 17 2 33 10 3 69 3 69 7 38 100 11 67 11 67 23 33 For transmitters rated at maximum output power 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 accordable to the transmitter manufacturer NOTE 1 At 80 MHz and 800 MHz the separation distance for the higher frequency range applies NOTE 2 Theseguidelinesmaynotapplyinallsituations Electromagneticpropag ationisaffectedbyabsorptionandreflectionfromstructures objectsan dpeople WA
21. RRANTY The device has a 2 year warranty starting from the purchase date covering electric and electronic parts for household use In case of purchase from professional operators purchase with an invoice the warranty is 12 months All of the parts subject to normal wear and tear ultrasound head are not covered by warranty as well as all the parts that are defective due to negligence improper maintenance tampering or repair work carried out by personnel that has not been authorised by the manufacturer or the authorised dealer The warranty conditions are those described under Warranty Regulations In accordance with the Medical Devices Directive 93 42 EEC the manufacturer must be able to trace the devices at any time in order to intervene promptly in case of manufacturing faults In the event of future repairs under warranty the equipment must be packaged to prevent damage during transport and sent to the manufacturer together with all of the accessories The purchaser only has the right to repair under warranty when the equipment is returned to the manufacturer complete with the receipt or invoice proving the correct origin of the product and purchase aate Warranty regulations 1 In the event f repairs under warranty the purchaser must include in the package the receipt or invoicing proving the purchase date 2 The electronic parts are covered by a 24 months 12 months for professional user warranty The warranty is gi
22. ard temperature reaches 80 C The device cannot work again unless the temperature is below 60 C Programs features I A C E R Srl It s possible to select parameters of user programs for each waveform TENS EMS IF 4P IF 2P and RUSSIAN The default parameters are indicated in the following tables Make reference to the tables with technical features indicated in the paragraph TECHNICAL FEATURES 19 Waveform PRG Phase CC CV Vector Vector Carrier Frequency C F High frequency Beat H Low Frequency Beat Time Auto Manual L 1 CC 0 45 4 0kHz 110Hz 100Hz 15 min 1 2 CC 0 45 4 0kHz 110Hz 100Hz 0 min 3 CC 0 45 4 0kHz 110Hz 100Hz 0 min 1 CC 0 45 4 0kHz 150Hz 100Hz 10 min Interferential 4 2 2 CC 0 45 4 0kHz 150Hz 100Hz 0 min poles 3 CC 0 45 4 0kHz 150Hz 100Hz 0 min 1 CC 0 45 4 0kHz 50Hz 50Hz 15 min 3 2 CC 0 45 4 0kHz 50Hz 50Hz 0 min 3 CC 0 45 4 0kHz 50Hz 50Hz 10 min 1 CC 0 45 4 0kHz 150Hz 90Hz 15 min IF AP 4 2 CC 0 45 4 0kHz 150Hz 90Hz 0 min 3 CC 0 45 4 0kHz 150Hz 90Hz 0 min 1 CC 0 45 4 0kHz 110Hz 100Hz 15 min 5 2 CC 0 45 4 0kHz 110Hz 100Hz 0 min 3 CC 0 45 4 0kHz 110Hz 100Hz 0 min 1 CC 0 45 4 0kHz 110Hz 100Hz 15 min 6 2 CC 0 45 4 0kHz 110Hz 100Hz 15 min 3 CC 0 45 4 0kHz 110Hz 100Hz 15 min 1 CC 0 45 4 0kHz 110Hz 100Hz 15 min 7 2 CC 0 45 4 0kHz 110Hz 100Hz 15 min 3 CC 0 45 4 0kHz 110Hz 100Hz 15 min 1 CC 0 45 4 0kHz 110Hz 100Hz 15 min 8 2 CC 0 45 4 0k
23. ch as following an injury or fracture Use caution following recent surgical procedures as stimulation may affect the patient s healing process Use caution if stimulation is applied over the menstruating or pregnant uterus Use caution if stimulation is applied over areas of skin that lack normal sensation Use this device only under the continued supervision of a licensed doctor therapist Electrical stimulation is ineffective for treatment pain of central nervous system Use extreme caution when treating patients who may not be able to report discomfort or pain Patients should not be left unattended during any treatment Keep this device out of the reach of children Unwanted effects Skin irritation inflammation and burns are potential adverse reactions Patients may experience headache and other painful sensations during or following the application of electrical stimulation near the eyes head and face and to the head and face In case of undesired effects suspend the therapy stop using the device straight away and contact your doctor Follow the instructions in order to minimise the undesired effects of the ultrasound therapy If the handpiece moves too slowly the patient may experience sharp and or deep peripheral pain If it moves too quickly or if the handpiece is not held correctly the therapeutic effects of the ultrasound might be reduced Some patients might be particularly sensitive to ultrasound and might therefore
24. d wave frequency 1MHz 10 3MHz 10 Duty cycle 10 100 stepping 10 Working frequency 100Hz Therapy time Adjustable max 30 minutes Output power 0 5W 10 0W when duty cycle 2 8096 for 5 cmq ultrasound head 0 5W 15 0V when duty cycle S 7056 for 5cmq ultrasound head 0 1W 2 0W when duty cycle gt 80 for 1cmq ultrasound head 0 1W 3 0W when duty cycle S 70 for 1cmq ultrasound head Effective radiating area Aer 1 0cmq optional 5 0cmq Effective intensity 3 0W cmq I A C E R Srl 28 Accuracy 20 when value gt 10 maximum value Rbn lt 8 0 Beam type Collimated Material of ultrasound head Aluminium Frequency 1 250Hz Frequency modulation F M 0 249Hz Burst rate Burst 1 10Hz Width impulse P Dur 30 400us Amplitude modulation A M IP Protection IPX7 only for ultrasound head 0 100 Output Interferential waveform 4 poles IF 4P 0 100mA CC at 1kOhm load 0 100V CV at 1kOhm load Therapy time Waveform Type Biphasic compensated Adjustable 1 60 minutes Contraction recovery Cycle Mode Selection CC constant current CV voltage current Continuous 4s 4s 4s 8s 7s 7s 5s 5s 4s 12s 10s 10s 10s 20s 10s 30s 10s 50s Ramp 1 seconds Kotz waveform Russian Waveform Type Vector Auto 0 100 Manual 0 90 Carrier f
25. e for programs features All parameters are adjustable by the user PROG FREQ DUTY CYCLE TIME SUGGERITED INT P 01 1MHz 50 14 min 1 0W cm2 P 02 1MHz 50 20 min 1 0W cm2 P 03 1MHz 50 20 min 1 0W cm2 P 04 1MHz 50 30 min 0 5W cm 1 0W cm P 05 1MHz 5096 16 min 1 0W cm P 06 1MHz 5096 14 min 1 0W cm P 07 1MHz 5096 14 min 1 0W cm P 08 1MHz 5096 14 min 1 0W cm P 09 1MHz 5096 14 min 1 0W cm P 10 1MHz 5096 14 min 1 0W cm I A C E R Srl 12 APPLICATIONS TREATMENT PRG HANDLE POSITION FREQ DUTY CYCLE TIME HEAD SUGGESTED INTENSITY NUMBERS Acne U 01 10 Affected area 3MHz 30 15 min 5 cmq 1 5W cm2 Free Muscle fatigue U 01 10 Affected area 1MHz 70 20min 5 cmq 2 W cm2 2 3 Algodystrophy U 01 10 Affected area 1MHz 5096 10 min 5 cmq 1 0W cm 1 5W cm 10 15 Anti inflammatory U 01 10 Affected area 1MHz 5096 15 min 5 cmq 1 0W cm 1 5W cm 10 15 Arthritis U 01 10 Affected area 1MHz 50 15 min 5 cmq 1 0W cm 1 5W cm 10 15 Fingers arthritis U 01 10 Hand fingers 1MHz 4096 15 min 1 1 5W cm 2W cm 10 15 Arthrosis U 01 10 Affected area 1MHz 5096 15 min 5 cmq 1 5W cm 2W cm 10 15 Bursitis U 01 10 Affected area 1MHz 3006 15 min 5 cmq 2W cm2 10 15 Brachialgia U 01 10 Trapezium and arm 1MHz 30 15 min 5 cmq 2W cm 10 15 Capsulitis U 01 10 Shoulder 1MHz 3096 15 min 5 cmq 2W cm 1
26. ellate ganglion on the spinal column after a laminectomy on the area surrounding the main nerves or the cranium should be avoided This device should not be used on ischemic tissues in individuals with vascular disease where the blood supply would be unable to follow the increase in metabolic demand and tissue necrosis might result This device should not be used over a healing fracture Avoid using ultrasounds near bone growth centres in kids growing children Electrotherapy contraindications Do not use this device on patients who have a cardiac pacemaker implanted defibrillator or other implanted metallic or electronic device because this may cause electric shock burns electrical interference or death Do not use this device on patients whose pain syndromes are undiagnosed Warnings for electrotherapy I A C E R Srl Do not apply stimulation over the patient s neck because this could cause severe muscle spasms resulting in closure of the airway difficulty in breathing or adverse effects on heart rhythm or blood pressure Do not apply stimulation across the patient s chest because the introduction of electrical current into the chest may cause rhythm disturbances to the patient s heart Do not apply stimulation over open wounds or inflamed areas or skin eruptions e g phlebitis thrombophlebitis varicose veins Do not apply stimulation over or in proximity to cancerous lesions Do not apply stimulation in presence of e
27. erved carefully This manual reflects the current state of machine technology and shall not be considered obsolete solely because updated at a later date on the basis of acquired experience The manufacturer reserves the right to update the production and the manuals with no obligation to update previous versions 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 SAFETY INFORMATION Cautions Read carefully the contraindications Respect the limitations and hazards associated with the use of the device Pay attention to the labels and symbols placed on the unit Always follow your prescribing doctor s or therapist s recommendations Do not operate this unit in an environment where other devices are used that intentionally radiates electromagnetic energy in an unshielded manner Do not use sharp objects such as pencil point or ballpoint pen to operate the buttons on the control panel Before each use inspect applicators and cables integrity The device should not be placed next to or on top of o
28. h the skin and make sure that the part is covered in gel so that the therapy is effective The green LED located next to the head on the handpiece lights up when the device is working Move the handpiace at a distance of 10 15 cm from pregelled electrode 21 The device has a head skin coupling system for lf i safety reasons If the contact is not correct and if e the intensity is set above 0 5W the LED on the HS handpiece and the symbol on the display will start flashing w 3v 22 It s possible to stop temporary the therapy at any time pressing the knob 3 Press again the knob to continue the treatment 23 Press the orange button Q to stop immediately the treatment in progress ATTENTION For safety patient the device is equipped with a protection system against high temperatures The device will stop electrical stimulation when the feature board temperature reaches 80 C The device cannot work again unless the temperature is below 60 C Moreover for patient safety the device will stop ultrasound treatment and LED starts flashing on the handle if the temperature is above 42 C It will start again when the temperature goes down to 41 C CLEANING MAINTENANCE AND STORAGE Before cleaning switch off the device and disconnect it from the mains supply Disconnect all cables and accessories The dust can be removed with a dry cloth To clean persistent dirt use a non abrasive liquid household cleaner no abra
29. imated 5 1 MHz 3 MHz 1 0 20 3 0 20 1 8cm R Max 5 0 Beam type collimated IPX7 sn ON OFF button GG Polarity of Power Supply QD Stop treatment Pill Start Pause button IPX7 Protected against the effects of immersion for ultrasound handle WEE Regulations Symbols and definitions Symbols and definitions E Ex Applied part type BF Interferential waveform with IF 4P 4 poles IF 2P Interferential waveform with 2 Russian waveform Kotz Russian TENS EMS waveforms TENS EW rN 4 Product in compliance with Directive 93 42 EEC MDD Electrotherapy channels DO electrotherapy ultr Attention Current can be higher than 10 mA r m s or 10 V r m s over 5 seconds period Fabricant name and address 5 98 q 1 indicators 0 0 y asound combined therapy symbols Program Ultrasound indicator CC Constant current Constant voltage S o ED 888 Parameter Timer Manufacturing date month year Attention Consult operating instructions LOT Ultrasound handle lot ER Serial number of ultrasound handle I A C E R Srl 10 INSTALLATION Remove the device and all accessories from shipping cartons Check the device equipment Follow the instructions below for a correct installation Connect the power supply
30. ing the external box dry all of the parts carefully before turning on the device Do not disassemble the device to clean or check it there is no need to clean the inside of the machine and in any case this operation should be performed by skilled technical personnel authorised by I A C E R srl I A C E R Srl 26 1 HO L i MEDICAL DIVISION When not using the device for a long time place it together with all its accessories in a dry place away from dust direct sunlight and protected from the weather Do not place other objects on top of the device To reset parameters follow the instructions below e Switch off the device e Keeping pressed simultaneously the knobs of electrotherapy channels 1 and 2 e Switch on the device by using ON OFF button 9 Keeping pressed the knobs 1 and 2 the device emits a prolonged signal for around 5 seconds and the set up frame will showed on the display OPERATION TROUBLES It s suggested to replace lead wires annually for a correct use I TECH UE was designed and manufactured using advanced technological solutions and high quality components for an efficient and reliable use Anyway should there be any problems during functioning please refer to this guide before contacting an authorised service centre The stimulation is not comfortable or painful Stimulation high intensity too Decrease the intensity The electrodes are too Repositi
31. lectronic monitoring equipment e g cardiac monitors ECG alarms which may not operate properly when the electrical stimulation device is in use Do not use the device in wet environment in bath or during shower Do not use the device when the patient is sleeping Do not apply stimulation while the patient is driving operating machinery or during any activity in which electrical stimulation can put the patient at risk of injury Consult with the doctor before using the device because the device may cause heart rhythm disturbances in susceptible individuals Apply stimulation only to intact clean healthy skin This device should not be used for symptomatic local pain relief unless etiology is established or unless a pain syndrome has been diagnosed Patients with arterial or venous thrombosis or thrombophlebitis are at risk of developing embolisms when electrical stimulation is applied over or adjacent to the vessels containing the thrombus If a patient has a history of deep vein thrombosis even many years past the affected area should not be stimulated Recent fractures should not be treated in order to avoid unwanted motion Stimulation should not be applied immediately after a trauma or to tissues susceptible to hemorrhage Do not apply electrodes directly over the eyes or inside body cavities Do not use electrical stimulation with high frequency surgical equipment or microwave or shortwave therapy systems Keep electrodes sepa
32. ng and place on the treatment area Insure that the entire electrode surface is in contact with patient skin As an alternative you can use silicon electrodes for electrotherapy treatments in two different ways e With the use of wet sponges e With the silicon electrodes and conductive gel The electrodes should be placed on the treatment area and hold down using the elastic belt supplied with the device os E Insert the cable with the Red connector into one rubber electrode Insert the cable with the Black connector into the other rubber electrode Make sure that the connectors are inserted completely into the electrode I A C E R Srl 17 I TECH OPTION 1 Insert the rubber electrode into the wet electrode sponge 5 6 OPTION 2 Put conductive gel on the rubber electrode surface before placing it on the skin Note use only CE marked gel or supplied by the fabricant 7 Use elastic belts to keep the electrodes in the right position ELECTROTHERAPY TREATMENT Pay attention to the follow indications to start electrotherapy treatment 8 1 Connect the black red cables to the sockets on the electrotherapy cables and connect this cable to the socket 12 on the back side of the device 2 Connect the electrodes to the electrotherapy cables following the instructions of the paragraph Preliminary Electrotherapy 9 Instructions 3 Switch on the device pressing ON OFF button placed laterally nex
33. on the electrodes closely Damaged broken Replace electrodes or cables electrodes or cables The effective electrodes area is too small Replace electrodes with ones that have an active area no less than 25 cm2 The stimulation is ineffective Improper electrodes Reposition or replace the electrodes Unknown Consult the doctor Display shows the error E1 or E2 Hardware problem Restart the device if the problem persists contact the fabricant Display shows the error E3 Temperature failure sensor The device will stop treatment automatically please wait at least 30 minutes before restart treatment PROBLEM POSSIBLE CAUSE SOLUTION Display does not switch on Wrong failed connection with power supply Check if the mains adapter is connected to the device and to power supply Check the integrity of all plugs sockets and connection cables Display shows the error E4 Excessive temperature of internal parts The device will stop treatment automatically please wait at least 30 minutes before restart treatment Display shows the error E5 Internal memory error Restart the device if the problem persists contact the fabricant ENVIRONMENT PROTECTION The Damaged broken Replace the electrodes stimulation is electrodes weak Electrodes not placed on the skin correctly Check the electrodes position
34. ot apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people Portable and mobile RF communications equipment should be used no closer to any part of the I TECH UE device including cables than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter Electromagnetic environment guidance Conducted RF IEC 61000 4 6 3V effective from 150kHz 80MHz to 3V Portable and mobile RF communications equipment should be used no closer to any 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 du to fixed RF transmitters an electromagnetic site survey should be considered If the measured field strength in the location in which the I TECH UE 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 I TECH UE 2 Over the frequency range 150 kHz to 80 MHz field strengths should be less than V V m I A C E R Srl 31 Recommended separation distances BETWEEN PORTAB
35. ound should be routinely checked before each use to determine that all controls function normally especially that the intensity control does properly adjust the intensity of the ultrasonic power output in stable manner Also determine that the treatment time control does actually terminate ultrasonic power output when the timer reaches zero Handle the handpiece with care to preserve its characteristics Before using the device pay attention to the appllicators and head integrity in order to avoid the ingress of liquids The ultrasound therapy controls unit is not designed to prevent the ingress of water or liquids Ingress of water of liquids could cause malfunction of internal components of system and therefore create risk of injury to the patient user Precaution for electrotherapy use The long term effects of chronic electrical stimulation are unknown Electrical stimulation is not a substitute for pain medications and other pain management therapies The safety of electrical stimulation during pregnancy has not been established Some patients may experience skin irritation or hypersensitivity due to the electrical stimulation or electrical conductive medium gel Patients with suspected or diagnosed heart disease should follow precautions recommended by their doctors Patients with suspected or diagnosed epilepsy should follow precautions recommended by their doctors Use caution when the patient has a tendency to bleed internally su
36. q 1 0W cm 1 5W cm 10 15 Pubalgy U 01 10 Internal thigh 1MHz 50 15min 5cmq 1 0W cm 1 5W cm 10 15 upper zone Radiculitis U 01 10 Affected area 1MHz 50 15 min 5 cmq 1 0W cm 1 5W cm 10 15 Muscle recovery U 01 10 Affected area 1MHz 7096 20 min 5 cmq 2 W cm2 Free Rizarthrosis U 01 10 Thumb area 1MHz 3006 15 min 5 cmq 1 5W cm2 10 15 Rizopathy U 01 10 Dorsal area 1MHz 60 15 min 5 1 5W cm 10 15 Wrinkle U 01 10 Affected area 3MHz 30 15 min 5 cmq 1 5W cm Free Sciatalgy U 01 10 Affected area 1MHz 5006 15 min 5 cmq 1 0W cm 1 5W cm 10 15 Stretch marks U 01 10 Affected area 3MHz 40 15 min 5 cmq 2W cm Free Venous stasis U 01 10 Extremities limbs 1MHz 5096 15 min 5 cmq 2W cm Free Sprains U 01 10 Affected area 1MHz 4096 15 min 5 cmq 2W cm 4 6 Muscle sprains U 01 10 Affected area 1MHz 4096 15 min 5 cmq 2W cm 8 10 I A C E R Srl 15 Tallonitis U 01 10 Heel 1MHz 5006 15 min 5 cmq 1 0W cm 1 5W cm 10 15 Tendinitis U 01 10 Affected tendons 1MHz 50 15 min 5 cmq 1 0W cm 1 5W cm 10 15 Stiff neck U 01 10 Cervical area 1MHz 5006 15 min 5 cmq 1 0W cm 1 5W cm 10 15 Carpal tunnel syndrome U 01 10 Internal wrist 1MHz 4096 15 min 5 cmq 1 0W cm 1 5W cm 10 15 Vascularisation U 01 10 Affected area 1MHz 6096 15 min 5 cmq 1 0W cm 1 5W cm Free Active principle vehiculation U 01 10 Affected area 1MHz 6096 15 min 5 cmq 2W cm
37. rated during treatment Electrodes in contact with each other could result in improper stimulation or skin burns Since the effects of stimulation of the brain are unknown stimulation should not be applied across the head and electrodes should not be placed on opposite sides of the head Precautions Ultrasounds should not be used on areas with reduced sensitivity or circulation Patients experiencing reduced sensitivity may not be able to warn their therapist doctor when the ultrasound is too intense Patients experiencing circulation problems may suffer from an excessive increase of temperature in the treated area If the patient feels a deep and sharp pain during the treatment the intensity must be reduced to a comfortable level The tendency to bleed is increased by the heat as more blood flows in the area Be careful when treating patients with bleeding disorders We advise moving the head if the intensity is more than 0 5 W sq cm Avoid heating or overheating the capsule in cases of acute and subacute arthritis This device should not be used for symptomatic local pain relief unless etiology is established or unless a pain syndrome has been diagnosed This device should not be used when cancerous lesions are present in the treatment area Cautions should be used for patients affected by the following diseases areas of the spinal column which underwent a laminectomy anesthesised areas patients with bleeding disorders Ultras
38. requency C F 4 0kHz High frequency Beat H Beat L 150Hz Low frequency Beat L 1 Beat H Biphasic compensated Mode Selection Output 0 100mA CC at 1kOhm load 0 100V CV at 1kOhm load CC constant current CV voltage current Carrier frequency C F Therapy time Adjustable 1 60 minutes 2 5kHz Burst Frequency Freq Interferential waveform 2 poles IF 2P 20 100Hz Waveform Type Biphasic compensated Mode Selection CC constant current CV voltage current Output 0 100mA CC at 1kOhm load 0 100V CV at 1kOhm load Duty cycle 1096 2096 3096 4096 5096 Therapy time Adjustable 1 60 minutes Contraction recovery Cycle Continuous 5s 5s 4s 12s 10s 10s 105 205 105 305 105 505 Ramp Carrier frequency C F 2 5kHz High frequency Beat H Beat L 150Hz Low frequency Beat L 1 Beat H 1 2e 5 seconds Output 0 100MA CC at 1kOhm load 0 100V CV at 1kOhm load Therapy time Adjustable 1 60 minutes Contraction recovery Cycle Continuous 5s 5s 45 125 105 105 105 205 105 305 105 505 Ramp 2 seconds TENS and EMS Waveform Type Monophasic or Biphasic compensated Mode Selection CC constant current CV voltage current I A C E R Srl 29 SYMBOLS Serial number of ultrasound handle
39. res by pressing B3 B7 buttons each waveform has different technical features e select frequency modulation vector Burst B4 select frequency carrier frequency B5 select duty cycle high frequency width modulation B6 select low frequency impulse duration B7 select therapy time contraction recovery cycle slope 18 I TEGN 10 11 12 Press the button of the selected parameter and regulate the value by using the knob 3 Place the electrodes on the area to be treated following the instructions of electrodes position manual In case of treatment with 4 poles interferential waveform place the electrodes as shown in the picture on the right Select the two channels intensity by using the knobs 1 2 placed on the left upper side of the front panel ATTENTION The device has a current supply safety system and the identification of the connected load in case of disconnected electrodes cables or damaged electrodes if the intensity is set above 10mA 10V the device emits an acoustic signal and the intensity value on the display starts flashing It s possible to stop temporary the therapy at any time pressing the knob 3 Press again the knob to continue the treatment Press the orange button to stop immediately the treatment progress ATTENTION For safety patient the device is equipped with a protection system against high temperatures The device will stop electrical stimulation when the feature bo
40. s for additional information regarding the application of Ultrasound To avoid the risk of electric shock disconnect the device from the electrical system before maintenance service Use of accessories transducers and cables other than those specified here even as internal spare parts may result in EM immunity reduction or in EM emissions increase The device must not be used in the same environment where magnetic resonance devices are working or are installed Contraindications Ultrasound therapy must not be performed near the uterus on pregnant women or those who suspect they might be pregnant Therefore the ultrasound beam should not be used in this area without ensuring that the patient is not pregnant This device should not be used over the thoracic area if the patient is using a cardiac pacemaker in order to avoid interferences between the ultrasound device and the pacemaker Do not direct the beam towards or near the eyes This device should not be used over cardiac area This device should not be used over neoplastic lesions Do not use near testicles not to increase their temperature The treatment with ultrasounds should be avoided in those areas affected by thrombophlebitis not to make the thrombus move Avoid treating patients with deep vein thrombosis embolism or arteriosclerosis Tissues that have previously been treated with X rays or other radiations should not be treated with ultrasounds Using ultrasounds on the st
41. sive no alcohol content solution If a more sterile cleaning is needed use a cloth moistened with an antimicrobial cleaner ATTENTION Do not immerse the device into liquids Should the device accidentally become submersed contact the fabricant and or Authorized Service center immediately Do not attempt to use a system that has been wet inside until inspected and tested by the fabricant or the Service Technician Certified by Authorized Service center Do not allow liquids to enter the ventilation holes in the optional modules Apply the protective film to the adhesive electrodes and store them in their packages after each use The electrodes are intended for single patient use only In case of irritations or reddening suspend the treatment and consult a doctor Use only CE marked electrodes and follow the instructions written in the package Clean the contact surface immediately after each treatment using a soft cloth or paper cloth lightly wet if needed Make sure that no ultrasound gel remains on the ultrasound head Aggressive clearing agents could damage the rubber insulation and shorten the life of the cables Clean the ultrasound head to remove gel after each use using a soft cloth or paper cloth lightly wet if needed Store the handpiece applicators cables with care at the end of each treatment To get more information about the original accessories and spare parts contact I A C E R Srl authorized centers After clean
42. t to power supply socket 4 Immediately after switching on the device carries out a self test around 10 seconds At the end of the self test display shows the last perfomed treatment I A C E R Srl 7 Press WAVEFORM 1 button show this icon indicates ELECTROTHERAPY treatment Select waveforms by using the knob 3 TENS EMS IF 4P Interferential 4 poles IF 2P interferential 2 poles RUSSIAN Kotz The icon related to the selected waveform starts flashing Select the program from P01 to P10 by pressing the PROGRAM CC CV B2 button the symbol P or S of the program starts flashing on the display There are two type of programs you can select programs with one phase P or with three phases S You can select the program by keeping pressed PROGRAM CC CV button for at least 5 seconds In the S programs display shows the phases total number and the number of the phase you want to set the parameters press B3 B7 buttons and the knob 3 to select programs parameters contraction recovery width impulse frequency etc for each phase please see the following instructions regarding each parameter Press the step knob to confirm the value for each phase m Select CONSTANT CURRENT CC or CONSTANTE rr VOLTAGE CV by pressing again PROGRAM CC CV button The unity of measurement changes from milliAmpere to V Volts rir LO Select the waveform featu
43. t where the ultrasound head is moved Connect the ultrasound handle to the socket 11 placed on the back side of the device Connect the cable when the device is switched off Switch on the device pressing ON OFF button placed laterally next to power supply socket Immediately after switching on the device carries out a self test around 10 seconds At the end of the self test display shows the last performed treatment c Press WAVEFORM MODE B1 button to show this icon indicates the COMBINED ULTRASOUND ELECTROTHERAPY treatment Select waveforms by using the knob 3 IF 2P TENS EMS and RUSSIAN Kotz singola P o a tre fasi S tenendo premuto per almeno 5 secondi il tasto PROGRAM CC CV Select the program from PO1 to P10 by pressing the PROGRAM CC CV B2 button the symbol P or S of the program starts flashing on the display There are two type of programs you can select programs with one phase P or with 12 13 14 15 16 I A C E R Srl three phases S You can select the program by keeping pressed PROGRAM CC CV button for at least 5 seconds In the S programs display shows the phases total number and the number of the phase you want to set the f parameters press B3 B7 buttons and the knob 3 to select programs parameters contraction recovery width impulse frequency etc for each phase please see the following instructions regarding each parameter Press the knob
44. tact with the skin and make sure that the part is covered in gel so that the therapy is effective The green LED located next to the head on the handpiece lights up when the device is working The device has a head skin coupling system for Kim safety reasons If the contact is not correct and if the intensity is set above 0 5W the LED on n nz the handpiece and the symbol on the display 1 will start flashing The system is not available on the 1cm head because of the reduced contact area the device emits an ultrasound beam even if the head is not in contact with the skin This is not a defect but rather a technical choice as it would be impossible to perform therapies on small and irregular areas like toes or fingers with such a system It s possible to stop temporary the therapy at any time pressing the knob 3 Press again the knob to continue the treatment Press the orange button to stop immediately the treatment in progress ATTENTION For patient safety the device will stop ultrasound treatment and LED starts flashing on the handle if the temperature is above 42 C It will start again when the temperature goes down to 41 C 11 I TEGO ATTENTION Only in the ultrasound mode the handpiece can be used for immersion treatments The handpiece and its cable are the only parts protected against water damage with a IPX7 grade Programs features and main applications Make reference to the following tabl
45. ther devices Should it prove necessary to place it next to or on top of other devices supervision is essential at all times to control its normal functioning Precautions must be taken regarding the electromagnetic compatibility of the device which must be installed and commissioned in compliance with the EMC provided in this manual I A C E R Srl 3 Warnings Portable RF devices can affect the functioning of the device Do not use mobile phones or other devices that emit electromagnetic fields nearby This may result in incorrect operation of the unit Only use the device for the recommended applications Do not use the device in presence of inflammable anesthetic mixture and in environments with high concentrations of oxygen I A C E R will not be held responsible for any accident if the above instructions are not complied with in full Make sure of the device connection to an electrical system in conformity with the current National laws Care must be taken when operating this equipment around other equipment Potential electromagnetic or other interference could occur to this or to the other equipment Try to minimize this interference by not using other equipment in conjunction with I TECH UE Before administering any treatment to a patient you should become acquainted with the operating procedures for each mode of treatment available as well as the indications contraindications warnings and precautions Consult other resource
46. ven through the point of sale or directly from the manufacturer 3 The warranty covers exclusively product damage causing operational defects 4 The warranty covers exclusively the repair or replacement free of charge including labour of components found to be defective in terms of manufacture or material 5 The warranty does not apply to damage caused by neglect or use not complying with the instructions provided damage caused by work carried out by unauthorized personnel or damage caused by accidental causes or the buyer s negligence with particular reference to external parts 6 The warranty does also not apply to damage to the equipment caused by incompatible power supplies 7 Parts subject to wear after use are excluded from the warranty 8 The warranty does not include transport costs to be paid by the purchaser in relation to the method and speed of transport 9 The warranty empire after 24 months 12 months for professional user After such time repair work will be carried out at the rates currently in force for the parts replaced and the labour and transport costs Any controversy will fall within the exclusive jurisdiction of the Venice courts FL I TECH UE All rights riserve I TECH UE and logo maia are owned by IACER and are registered I A C E R Srl 32 I TECH I A C E R Srl 33 Sede Amministrativa magazzino 30030 MARTELLAGO VE Via S Pertini 24 A Tel 0039 041 540135
47. z 5096 15 min 5 cmq 1 0W cm 1 5W cm 10 15 Dorsalgy U 01 10 Dorsal area 1MHz 50 15 min 5 cmq 1 0W cm 1 5W cm 10 15 Drainage U 01 10 Affected area 1MHz 6096 15 min 5 2W cm 30 Eczemas U 01 10 Affected area 3MHz 50 15 min 5 cmq 1 0W cm 1 5W cm 10 15 Oedemas U 01 10 Affected area 1MHz 3006 15 min 5 cmq 2W cm2 10 15 Hematomas U 01 10 Affected area 1MHz 40 15 min 5 cmq 2W cm 3W cm 10 15 Epicondylitis U 01 10 Elbow 1MHz 40 15 min 5 cmq 1 0W cm 1 2W cm 10 15 Epitrocleitis U 01 10 Internal elbow 1MHz 4096 15 min 5 cmq 1 0W cm 1 2W cm 10 15 Slipped disc U 01 10 Affected area 1MHz 5006 15 min 5 cmq 1 0W cm 1 5W cm 10 15 Gonarthrosis U 01 10 Knee 1MHz 50 15 min 5 cmq 1 5W cm 2W cm 10 15 I A C E R Srl 14 Lymphoedema U 01 10 Affected area 1MHz 30 15 min 5cmq 2W cm 10 15 Lypolisis U 01 10 Affected area 1MHz 6096 15 min 5 cmq 2W cm 30 Lumbago U 01 10 Lumbar area 1MHz 5096 15 min 5 cmq 1 0W cm 1 5W cm 10 15 Massage U 01 10 Affected area 1MHz 7096 20min 5 cmq 2 W cm2 Free Mialgy U 01 10 Affected area 1MHz 50 15 min 5 cmq 1 0W cm 1 5W cm 10 15 Mononeuropathy U 01 10 Pain zone 1MHz 5096 15 min 5 1 5W cm 12 15 Neuralgia U 01 10 Affected area 1MHz 50 15 min 5 1 0W cm 1 5W cm 10 15 Periarthritis U 01 10 Shoulder 1MHz 7096 15 min 5 cm

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