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Related Manuals for I-Tech I-TECH.AR
Summary of Contents for I-Tech I-TECH.AR
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Page 1: User Manual
USER MANUAL MNPG112 Rev.2- 17-05-2013... -
Page 2: Table Of Contents
INDEX TECHNICAL PROBLEMS ..................16 ELECTROMAGNETIC INTERFENCES ............... 16 INFORMATION ON THE MANUAL ................1 WRITING CONVENTIONS .................... 1 TROUBLESHOOTING CHART ................. 16 WARRANTY ......................2 TECHNICAL FEATURES ..................17 NOTES ........................2 APPENDICES ....................... 18 Appendix A – ENVIROMENTAL PROTECTION ............18 CAUTIONS ...................... -
Page 3: Information On The Manual
- exceptional events. This document provides valuable information regarding the installation, set up and use of I-TECH.AR. Please contact the manufacturer to get further information. It is a useful and essential reference guide for the user: read the contents of the N.B. -
Page 4: Warranty
carefully clean and disinfect all parts of the machine and accessories which have been in contact with patients; I.A.C.E.R. guarantees the quality of its products for a period of 24 months from the Any equipment which the technical department does not consider hygienic (Italian date of purchase, when information contained in this manual regarding installation, law T.U.S. -
Page 5: Warnings
- The therapeutic suggestions are stored in the permanent memory of the machine. These For optimal use of the apparatus and to ensure its optimum performances it is protocols can be edited but not possible to save any changes. recommended to perform properly within the time and in the manner recommended - The protocols of therapeutic suggestion preloaded on the machine cannot be deleted. -
Page 6: Introduction To The Tecnology
Patients with implanted electronic devices (eg pacemakers) should not be subject to tecar The cleaning and disinfection must be done systematically before the therapeutic therapy without the consent of the physician. treatment which subject the patient. Avoid use in areas having ongoing inflammatory processes. Non spruzzare, ne’... -
Page 7: Techniques Of Application
I-TECH.AR stimulates the increase of blood flow in a direct manner, thanks to the location of the more point resistive or capacitive to the affected area (e.g., the increase of temperature, and indirectly through the oxygen demand from the treated popliteal groove in treatment of the knee). -
Page 8: Intended Use
− Musculoskeletal disorders: muscle strains, contractures, tears, myositis and disorders involving tendons, ligaments, joint capsules. I-TECH.AR is an electro-medical device that delivers tecar-therapy treatments, with CONTRA-INDICATIONS the help of probes/applicators for the provision of treatment. I trattamenti di tecar-terapia non possono essere erogati su: The use of this equipment is reserved for operators that, by their training, provide assurance of proper use and safe for the patient. -
Page 9: Settings Up
Be very careful when removing the contents of the pack. The unit and accessories are wrapped in transparent sheets of polyethylene protection and contains the following: − the User Manual; − n.1 mains power supply cable; − n.2 spare fuses (see technical specifications); −... -
Page 10: Accessories
ACCESSORIES L’apparecchio è fornito del cavo di alimentazione di rete, and it can be used with following accessories forniti in dotazione: Optional Description Supplied Power cable supply (spina schuko) Spare FUSES (see technical specifications) User manual Smart-card Capacitive probe Kit 3 capacitive electrodes (diameters 30,50,70) Resistive probe Kit 3 resistive electrodes (diameters 30,50,70) Metallic mass (steel plate) -
Page 11: Device Description
Color graphic LCD display Rear panel Encoder control knob Connector for probes Programming panel Connector for plate I.A.C.E.R. Srl... - Page 12 PROGRAMMING PANEL REAR PANEL Ventola di aerazione Audio connector Integrated power Ground (not used) module Window for connection SMART-CARD USB connector, used for processor setting SMART-CARD OUTPUT PANEL ACCESSORIES Capacitive and resistive probes Connectors for PROBES Connector for STEEL PLATE Capacitive electrodes Resistive electrodes I.A.C.E.R.
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Page 13: How To Use Of The Device
This section provides important information and instructions on how to make the best use of the equipments for tecar-therapy I-TECH.AR. All the control functions and the machine itself are handled and co-ordinated by a microprocessor: apart from making pre-memorised programmes available for application, the microprocessor ensures that the machine can be personalised and operated in a highly safe and efficient manner. -
Page 14: Various
Turn the encoder you select the settings that you want to change, then pressing this knob confirms the choice. SETTINGS The screen displays also the version of the software and of firmware modules Variuos installed on the equipment, and contacts of the company. Language Default Pressing the button EXIT, to return to the screen of the fig.2. -
Page 15: Language
Pressing the EXIT button to cancel the format operation of the selected memory To save the combination of values selected press the SAVE button, or press the EXIT support and returns to the screen in fig.4. Pressing again the EXIT button to return to button to cancel the operation. -
Page 16: Loading Programs
If you press the STOP button the emission finally ends and you return to the screen in Pressing the EXIT button (whatever the memory selected) returns to the screen of the fig.8. fig.2. Pressing the EXIT button returns you to the screen in fig.2. To start the desired treatment, turn the encoder knob to reach the desired protocol, then press it to confirm the selection. -
Page 17: Maintenance
Fig.11 Fig.12 DEFAULT DEFAULT The I-TECH.AR device for endodiathermy do not require any particular maintenance Modality:sequence Modality:sequence operations , but only a periodic maintenance and cleanliness of the probes, in order Capacitive Capacitive to ensure the better operating conditions, guarantee the effectiveness of the... -
Page 18: Index Technical Problems
EMC measures within the company. front panel turn The I-TECH.AR equipment does not generate significant radio frequency energy and is adequately immune to radiated electromagnetic fields. Some controls on Faulty keys or buttons. Therefore it does not detrimentally interfere with radio-electric communications, the front control Contact I.A.C.E.R. -
Page 19: Technical Features
of wear on head and cable. Resistive use 105 V max. Resistive probe Failure in electronic current Contact I.A.C.E.R. Srl service Probes supplied generator circuit. centre. Capacitive probe Carry out prescribed Emission Frequency of the probe 455 kHz maintenance. Install and Resistive, made of stainless steel Non perfectly efficient position unit as described. -
Page 20: Appendices
Appendix A – ENVIROMENTAL PROTECTION The product must be dispose of as “electronic waste”, not as “domestic waste” The device I-TECH.AR were designed and engineered to have minimal negative environmental impact, in consideration of their operational and safety requirements. Input features... -
Page 21: Appendix C - Therapeutic Treatment
Appendix C – THERAPEUTIC TREATMENT MODALITY ELECTRODE RETURN DURATION PROTOCOL POWER N° SESSIONS DIM.**** PLATE** (MINUTES) CAPACITIVE RESISTIVE Contusions LOW LIVEL Myalgia Medium livel Relief treatment of muscles Medium livel Distorsions Medium livel Lumbago Medium livel Lumbo-sciatica Medium livel Muscle pathologies Max livel(300) Tendon lesions Medium livel... -
Page 22: Appendix E - Electro-Magnetic Compatibility Tables
Appendix E – ELECTRO-MAGNETIC COMPATIBILITY TABLES Guidance and manufacturer’s declaration – electromagnetic immunity FOR ALL ME EQUIPMENT Guidance and manufacturer’s declaration – electromagnetic emissions The ME EQUIPMENT is intended for use in the electromagnetic environment specified below. FOR ALL ME EQUIPMENT The customer or the user of the ME EQUIPMENT should assure that it is used in such an The ME EQUIPMENT is intended for use in the electromagnetic environment specified below. - Page 23 Guidance and MANUFACTURER’S declaration – electromagnetic IMMUNITY – FOR ME EQUIPMENT THAT ARE NOT LIFE-SUPPORTING Recommended separation distances between portable and mobile RF communications equipment and the 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 environment.
- Page 24 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. VE001767 e-mail: iacer@iacer.it Internet: www.itechmedicaldivision.com...