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IACER I-TECH LA500 User Manual

Laser therapy
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USER MANUAL
MNPG127 rev.02 10/03/19
Laser therapy

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Summary of Contents for IACER I-TECH LA500

  • Page 1 USER MANUAL MNPG127 rev.02 10/03/19 Laser therapy...

  • Page 3: Table Of Contents

    Summary SUMMARY TECHNICAL INFORMATION NFORMATION ON THE USER MANUAL ANUFACTURER ECLARATION OF CONFORMITY LASSIFICATION URPOSE AND SCOPE ECHNICAL FEATURES EVICE AND COMMAND DESCRIPTION ABELS Package content OTES PURPOSE NTRODUCTION TO THE TECHNOLOGY NDICATIONS ONTRA INDICATIONS ARNINGS ATIENT PREPARATION NSTRUCTION FOR USE Therapeutic indications !Warning! DEVICE’S CARE...

  • Page 5: Technical Information

    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.

  • Page 6: Manufacturer

    I.A.C.E.R. S.r.l. Via S. Pertini, 24/a • 30030 Martellago (VE) Tel. 041.5401356 • Fax 041.5402684 IACER Srl. is an Italian manufacturer of medical devices (certified CE no. MED24021 from the Notified Body no. 0476, Kiwa Cermet Italia Spa). Declaration of conformity I.A.C.E.R.

  • Page 7: Classification

    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. IACER Srl MNPG121...

  • Page 8: Technical Features

    810 ± 30nm Laser classification DNRO (m) Divergence 260mrad Impulse duration Emission CONTINUOUS Adjustable percentage of emitted 0% - 100% power Emission frequency Pulsed mode ON/OFF (sec) Pointing led Red light 650nm±30nm Classification in compliance with the directive 93/42/EEC IACER Srl MNPG121...
  • Page 9 +5 - +40°C temperature Conditions of use Relative humidity < 80 % without condensation Environmental +5 - +40°C temperature Storage/transport Relative humidity <93% without condensation conditions Atmospheric 700-1060hPa pressure The useful life of the device is 5 years. IACER Srl MNPG121...

  • Page 10: Device And Command Description

    Device and command description Labels IACER Srl MNPG121...
  • Page 11 Symbol Meaning Warning, see document in attachment with the product. Manufacturer’s logo. CE product mark released by the Notification Body no. 0476. Class of isolation I with applied part type B according to EN 60601-1 ed. III^. IACER Srl MNPG121...

  • Page 12: Package Content

    The product must be disposed as “electronic waste”, in accordance to WEEE Directive on waste electrical and electronic equipment. Read instructions for use. Wear protection glasses. Package content The I-TECH LA500 box contains: • N°1 mainframe; • N°2 safety keys; •...

  • Page 13: Purpose

    “stimulating” action on mitochondrial functions with a higher production of ATP. The applications of the I-TECH LA500 laser produce several effects on the treated tissues: 1. increase in hematic flow: vasodilatation of capillaries and arteries 2.

  • Page 14: Indications

    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;...

  • Page 15: Contra-Indications

    Other: Atopic dermatitis and eczema in the acute phase. Inflammatory processes in place at the site to be treated. Abrasions or bruises. Photoallergy. Photodermaititis. IACER Srl MNPG121...

  • Page 16: Warnings

    Do not use accessories other than the ones provided: they might damage the unit, causing the warranty to become void. In case you have any problems or difficulties with installation, contact IACER Srl technical support. If using the same extension for the unit and other units, make sure...

  • Page 17: Patient Preparation

    For security reasons, the software to be downloaded in the devices are only the ones specific to the device in question. In case of wrong software installation, the device could immediately stop its functions, requiring the intervention of IACER Srl technical assistance. Patient preparation Before applying the laser therapy, it is necessary to prepare the skin of the patient.
  • Page 18 AC) and switch on the device moving the key button on the “ON” position, which 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-set on CONTINUOS mode and the treatment time last 3 minutes.
  • Page 19 If you need to stop the treatment before the end, press the STOP button and the device will stop immediately the laser emission. In case of an emergency stop press the red button placed on the back of the machine. IACER Srl MNPG121...

  • Page 20: Therapeutic Indications

    NEK PAIN (acute pain) 200s 800s NEK PAIN (chronic pain) 160s LUMBALGY 200s BURSITIS 264s BAKER’S CYST 264s DE QUERVAIN SYNDROME 100s 400s OEDEMA 264s HEMATOMA 264s EPICONDYLITIS 200s HERNIATED DISC 200s TENDINITIS 100s 400s CARPAL TUNNEL SYNDROME 264s IACER Srl MNPG121...

  • Page 21: Warning

    IACER Srl shall not be consider responsible for any accidents. THE USE OF THE CONTROLS OR REGULATIONS OR THE EXECUTION...
  • Page 22 The use of the device is absolutely forbidden in presence of anesthetic inflammable substances and in full oxygen environment. IACER 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.

  • Page 23: Device's Care

    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 starting a new treatment.

  • Page 24: Troubleshooting

    Fuse/s is/are Replace missing, defective defective interrupted. interrupted fuse/s. The control electric Contact IACER service circuit is broken. center. Defective The LCD display in components in the Contact IACER service the frontal panel control electric center.

  • Page 25: Disposal

    • the device has been exposed to rain. Disposal The therapeutic laser devices I-TECH LA500 were designed and engineered to have minimal negative environmental impact, in consideration of their performance and safety requirements, following the disposition given by the European Directive 2012/19/EU, regarding the waste electrical and electronic equipment.

  • Page 26: Warranty

    Warranty IACER Srl guarantees a warranty period, unless information contained in this manual regarding installation, use and maintenance is strictly adhered. For more information on the warranty please contact the distributor or vendor, in order to check the norm and standard in force in your Country, or ultimately the manufacturer IACER Srl.

  • Page 27: Support

    Spare part The manufacturer makes available at any time the original spare parts for the equipment. Please contact: I.A.C.E.R. S.r.l. Via S. Pertini, 24/a • 30030 Martellago (VE) IACER Srl MNPG121...

  • Page 28: Electromagnetic Interferences And Electromagnetic Compatibility Tables

    (see also paragraph Warnings). Electromagnetic interferences electromagnetic compatibility tables The I-TECH LA500 equipment has been designed and manufactured according ELECTROMAGNETIC COMPATIBILITY DIRECTIVE 2014/30/EU with the aim of providing adequate protection from harmful interference when installed in homes and health establishments.
  • Page 29 CISPR 11 establishments, other than Harmonic emissions domestic establishments Class A IEC 61000-3-2 those directly connected to the public low voltage power supply Voltage fluctuations/ network that supplies buildings flicker emissions Complies used for domestic purposes. IEC 61000-3-3 IACER Srl MNPG121...
  • Page 30 0% U 0% U continued operation input lines per 1 cycle per 1 cycle during power mains IEC 61000-4-11 interruptions, it is 70% U 70% U recommended that the 25/30 25/30 device be powered from cycles cycles IACER Srl MNPG121...
  • Page 31 (50/60Hz) magnetic at levels characteristic of 3A/m 3A/m field a typical location in a IEC 61000-4-8 typical commercial or hospital environment NOTE: U is the ac mains voltage prior to application of the test level. IACER Srl MNPG121...
  • Page 32 (m). Field strengths from fixed RF transmitters, as determined by an electromagnetic site survey, could be less than the compliance level in each frequency range. Interference may occur near equipment marked with the following symbol: IACER Srl MNPG121...
  • Page 33 NOTE (1) At 80MHz and 800MHz, the separation distance for the higher frequency range applies. These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people. IACER Srl MNPG121...
  • Page 34 I-TECH LA500. All rights reserved. I-TECH LA500 and the logo property exclusively of I.A.C.E.R. Srl and registered. IACER Srl MNPG121...

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