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IACER Srl 

30 

MNPG179 

PROBLEM 

POSSIBLE CAUSE 

SOLUTION 

Some components on the 
electronic  control  circuit 
are defective. 

Contact 

the 

manufacturer 

The 

power 

supply 

sections  of  the  laser 
sources are defective. 

The 

equipment 

works 

properly 

but  there  is  an 
evident  decrease 
in the efficiency of 
treatment. 

The  laser  sources  are 
worn out or defective. 

Contact 

the 

manufacturer 

The  current  generating 
circuit  in  the  equipment 
may be defective. 

The 

equipment 

does  not  turn  on 
or  appears  to 
work properly but 
there 

is 

no 

emission. 

Loss  of  pressure  in  the 
actuator. 

Check air-tightness. 

When  any  of  the  following  conditions  occur,  unplug  the  equipment  and 
contact the IACER Srl technical assistance service: 

 

the  cable  or  rear  integrated  power  supply  module  are  worn  or 
damaged; 

 

liquid has entered the equipment; 

 

the equipment has been exposed to rain. 

 

-

 

Only authorized technical staff from the manufacturer may access the 

internal parts of the equipment. 

-

 

Please contact IACER Srl or its authorized service centers for repairs 

and further information.

 

!CAUTION! 

-

 

DO NOT open the device: the HIGH VOLTAGE inside can be 

DANGEROUS. 

Disposal 

The therapeutic laser devices I-TECH LA8000/LA10000 were designed and 
engineered  to  have  minimal  negative  environmental  impact,  in 

Summary of Contents for I-TECH LA8000

Page 1: ...USER MANUAL MNPG179Rev 2of03 07 2019 Laser therapy...

Page 2: ......

Page 3: ...TECHNOLOGY 11 INDICATIONS 13 CONTRAINDICATIONS 13 WARNINGS 14 PATIENT PREPARATION 16 INSTRUCTIONS FOR USE 16 Warning 16 Connections 18 Start up and protection password 18 Main menu 19 Program selectio...

Page 4: ...IACER Srl ii MNPG179...

Page 5: ...ept at hand for quick reference and correctly stored The manufacturer declines all responsibility for improper use of the device use contrary to specific national laws incorrect installation defective...

Page 6: ...D24021 from the Notified Body no 0476 Kiwa Cermet Italia Spa Declaration of conformity I A C E R S r l Via S Pertini 24 A 30030 Martellago Ve Italia herewith declares under its own responsibility that...

Page 7: ...on EN 60825 1 equipment unsuitable for use in presence of a flammable anesthetic mixture containing air oxygen and nitrous oxide equipment suitable for continuous operation equipment unsuitable for ou...

Page 8: ...tt Two delayed type fuses T T2 5A Backlit LCD display 128x64 pixel graphic display Power Settable from 1W to 8W 10W 3 Emission wavelength of laser diode 974nm 3nm Laser classification IEC 60825 1 Clas...

Page 9: ...he skin Around 38 mm Spot area Around 10mm2 3 Operating conditions environmental temperature From 10 C to 40 C relative humidity From 15 to 93 without condensation atmospheric pressure 500 1060 hPa Co...

Page 10: ...IACER Srl 6 MNPG179 Device and command description...

Page 11: ...IACER Srl 7 MNPG179 Labels...

Page 12: ...cs connector LABEL 4 Placed on one side of the device in warns on the danger of the laser radiation LABEL 5 Placed on one side of the device LABEL 6 Placed on the back of the device it resumes the pri...

Page 13: ...12 It indicates the emergency stop button LABEL 13 It indicates the position of the laser aperture Symbol Meaning Manufacturer s logo CE product mark released by the Notification Body no 0476 Class of...

Page 14: ...o wear protective glasses Packaging content The I TECH LA8000 LA10000 box contains n 1 user manual n 1 power supply cable shuko plug n 2 spare fuses see table Technical features n 1 handpiece n 1 peda...

Page 15: ...therefore permits immediate alleviation of the symptoms of inflammation and degeneration in the fields of orthopedics neurology and dermatology and reduces healing time it is also a valid form of ther...

Page 16: ...e deep stimulation of tissue for rapid and uniform cell regeneration the I TECH LA8000 10000 permits deep stimulation for treating internal tissue and structures like the articulation of the femur and...

Page 17: ...t exposure to eyes class 4 lasers are potentially harmful to the retina although the likelihood of damage to the retina is extremely low The operator must however wear the special safety glasses provi...

Page 18: ...and drugs triggers this response It is recommended that patients at allergic risk or patients with a history of such reactions are tested with a minimum time of treatment Means of fixation metal plate...

Page 19: ...the I TECH LA8000 After carefully inserting the fiber optic in the socket turn the locking ring clockwise to the end of its stroke without forcing it In any case turn the locking ring to bring the ref...

Page 20: ...follows 1 clean the skin with care where the head of the laser is to be positioned using either water and soap or alcohol 2 dry the skin thoroughly Cleaning and disinfection must be carried out syste...

Page 21: ...the energy settings configured on the display For this reason keep the handpiece in contact with the affected area during emission of the laser After activating the handpiece by means of contact with...

Page 22: ...e socket on the front panel fastening carefully the connector so that the mark on the connector of the handpiece will be aligned with the mark on the front panel of the device ATTENTION do not strain...

Page 23: ...from 0 4 to 10 mm2 The equipment works most efficiently with the spacer fully extended for a laser output of 10mm2 This special HANDPIECE therefore ensures a broader range of action and a higher degre...

Page 24: ...igger point mode while the second is in scanning mode The operator is free to choose whether to proceed with the second phase or not the settings of the second phase appear at the end of the first one...

Page 25: ...returns to the main menu PROGRAMS LIST N Name Watt s Cycle Hz Duty Cycle Time r min Punti p Area cm2 Joule cm2 1 Analgesic 1 1 100 50 4 4p 120J 2 Analgesic 2 5 200 60 5 50cm2 18J cm2 3 Neck pain 1 1 1...

Page 26: ...cm2 25 Muscle injuries 4 500 30 5 25cm2 14J cm2 26 Meniscopathy 2 500 50 2 5cm2 24J cm2 27 Sinovitis 4 1000 30 6 25cm2 17J cm2 28 Muscle Strain 6 500 30 10 25cm2 43J cm2 29 Tendinopathy 2 100 40 2 5cm...

Page 27: ...f the LA10000 This parameter does not change in relation to the other parameters Cycles For enabling and modulating the laser emission The first choice is Continuous where the emission of the laser is...

Page 28: ...mit the laser it permits a pause with the actuator not pressed of no more than 3 minutes After this length of time the device disables the laser and returns to the main menu ENTER key during therapy t...

Page 29: ...ime in order to determine the diode s lifetime It is a parameter useful to the manufacturer used for the device electronic problems resolution Device scare Maintenance For safety reasons ALWAYS turn o...

Page 30: ...ore carrying out any maintenance or cleaning operations It is strictly recommended not to use diluents detergents acid solutions aggressive solutions or flammable liquids to clean the external surface...

Page 31: ...to replace correctly the fuses on the back of the device follow the instructions below turn off the equipment unplug the equipment use a screwdriver to open the fuse holder tray making sure to insert...

Page 32: ...mble the handpiece applicator this could result in damage to the handpiece and render the warranty null and void Do not for any reason disassemble the equipment for the purpose of cleaning or inspecti...

Page 33: ...nnector of the equipment The power cable is worn and damaged Replace the power cable The emergency switch is turned off Turn on the emergency switch One or more of the fuses are defective or damaged R...

Page 34: ...s of pressure in the actuator Check air tightness When any of the following conditions occur unplug the equipment and contact the IACER Srl technical assistance service the cable or rear integrated po...

Page 35: ...or further information on the obsolete equipment disposal please contact the dedicated disposal service or the shop in which the device was bought Warranty IACER Srl guarantees a warranty period unles...

Page 36: ...which have been in contact with patients Any equipment which the technical department does not consider hygienic Italian law D Lgs 81 2008 on safety in the workplace will not be accepted 3 disassembl...

Page 37: ...nstalled in homes and health establishments The equipment does not generate significant radio frequency energy and is adequately immune to radiated electromagnetic fields Therefore it does not detrime...

Page 38: ...ns CISPR 11 Group 1 The device must emit electromagnetic energy at RF in order to perform its intended function So its RF emissions are very low and therefore it does not affect electronic equipment p...

Page 39: ...material the relative humidity should be at least 30 Transistor Electri cal fast transient IEC 61000 4 4 2kV for power supply lines 2kV per power supply lines Mains power quality should be that of a t...

Page 40: ...environment guidance 70 UT 30 dip in UT for 25 cycles 5 UT 95 dip in UT per 5s 70 UT 30 dip in UT for 25 cycles 5 UT 95 dip in UT per 5s power mains interruptions it is recommended that the device be...

Page 41: ...ation distance Conducted RF IEC 61000 4 6 3Vrns from 150kHz to 80MHz 6Vrms from 150kHz to 80MHz in ISM band 3Vrns from 150kHz to 80MHz 6Vrms from 150kHz to 80MHz in ISM band P V d 1 5 3 P V d 1 12 for...

Page 42: ...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...

Page 43: ...800 ISM band 80 800 800 6 to RF wireless radio communication equipment 0 01 0 12 0 2 0 12 0 23 0 1 0 38 0 63 0 38 0 73 0 2 1 1 20 2 0 1 20 2 30 1 8 2 10 3 80 6 3 3 80 7 30 100 12 00 20 12 00 23 00 Fo...

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