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JSC "MILTA - HUMANITARIAN-INFORMATION TECHNOLOGIES DESIGN & PRODUCTION COMPANY" ( - ) DEVICE FOR

JSC "MILTA - HUMANITARIAN-INFORMATION TECHNOLOGIES DESIGN & PRODUCTION COMPANY"

( - )

DEVICE FOR COMBINED PHOTO-MAGNETIC- INFRARED LASER THERAPY
DEVICE FOR COMBINED PHOTO-MAGNETIC- INFRARED LASER THERAPY
DEVICE FOR COMBINED PHOTO-MAGNETIC- INFRARED LASER THERAPY

DEVICE FOR COMBINED PHOTO-MAGNETIC- INFRARED LASER THERAPY

& PRODUCTION COMPANY" ( - ) DEVICE FOR COMBINED PHOTO-MAGNETIC- INFRARED LASER THERAPY Revision 2/2010
& PRODUCTION COMPANY" ( - ) DEVICE FOR COMBINED PHOTO-MAGNETIC- INFRARED LASER THERAPY Revision 2/2010
& PRODUCTION COMPANY" ( - ) DEVICE FOR COMBINED PHOTO-MAGNETIC- INFRARED LASER THERAPY Revision 2/2010
& PRODUCTION COMPANY" ( - ) DEVICE FOR COMBINED PHOTO-MAGNETIC- INFRARED LASER THERAPY Revision 2/2010
& PRODUCTION COMPANY" ( - ) DEVICE FOR COMBINED PHOTO-MAGNETIC- INFRARED LASER THERAPY Revision 2/2010
& PRODUCTION COMPANY" ( - ) DEVICE FOR COMBINED PHOTO-MAGNETIC- INFRARED LASER THERAPY Revision 2/2010
& PRODUCTION COMPANY" ( - ) DEVICE FOR COMBINED PHOTO-MAGNETIC- INFRARED LASER THERAPY Revision 2/2010
& PRODUCTION COMPANY" ( - ) DEVICE FOR COMBINED PHOTO-MAGNETIC- INFRARED LASER THERAPY Revision 2/2010

Revision

2/2010

Operating Manual

CONTENTS

1. INTRODUCTION

4

2. GENERAL INFORMATION

5

3. SAFETY PRECAUTIONS

6

4. INTENDED USE

8

5. TECHNICAL CHARACTERISTICS

10

6. DELIVERY SET

11

7. THE DEVICE DESIGN

13

8. THE DEVICE SETUP

16

9. THE DEVICE OPERATION

17

10. MAINTENANCE

22

11. TROUBLESHOOTING

23

12. PACKING, STORAGE AND TRANSPORTATION

24

13. MANUFACTURER'S WARRANTY

25

14. ACCEPTANCE CERTIFICATE

26

WARRANTY CARD

27

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Operating Manual

1.

INTRODUCTION

1.1. We can hardly meet somebody who never had pain. Pain is a symp- tom or sign of something wrong in an organism. And pain is a signal of incipient disease or a disease in progress. Medicine has contrived variety of methods to defeat pain but, unfortunately, these methods don't delete a disease as if concealing a disease inside an organism.

Owing to long-term investigations of big group of scientists, physi- cians, engineers, geneticists, biophysicists and clinicians of Russia there has been designed the first-in-the-world medical device of new type called RIKTA -ESMIL (hereinafter referred to as "the De- vice"). The Device not only eliminates acute and chronic pain but al- so allows treating the disease which provokes the pain.

1.2. All rights for the Device are protected by a series of patents. The trademark is reserved in many countries of the world.

1.3. The Device is produced by JSC MILTA-PKP GIT which quality sys- tem is certified according to the International standard ISO

13485:2003.

1.4. RIKTA e-ESMIL device ESMIL (2A).

1.5. The Device is registered in the Russian Federation and is entered in the State Register of medical devices. Registration certificate No.

is produced under trademark RIKTA -

29/06050703/5754-03.

is produced under trademark RIKTA - 29/06050703/5754-03. 1252 1.6. The Device is certified in the Russian
1252
1252

1.6. The Device is certified in the Russian Federation. Certificate of Compliance No. RU. 2. 16714.

1.7. The Device meets the requirements of Medical De- vice Directive 93/42 EEC annex II.

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2. GENERAL INFORMATION

2.1. Please carefully read and understand the Operating Manual before attempting to operate the Device.

2.2. The Operating Manual (hereinafter referred to as "the Manual") is the document that certifies basic parameters and technical charac- teristics of the Device and contains instructions for the Device opera- tion, maintenance, troubleshooting, transportation and storage.

2.3. The Manual shall be kept during all the Device service life.

2.4. The treatment using the Device shall be made in accordance with the Methodical Recommendations which are delivered with the De- vice.

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Operating Manual

 

3.

SAFETY PRECAUTIONS

3.1.

The person(s) who will operate the Device must thoroughly learn the Operating Manual and the applied Methodical Recommendations be- fore undertaking any operation.

3.2.

Disassembling of the Device is STRICTLY PROHIBITED.

 

3.3.

Plug the AC/DC adapter in wall outlet against stop.

3.4.

To avoid electric shock DON'T PLUG IN the AC/DC adapter if your hands are wet.

3.5.

lug/unplug connector of AC/DC adapter in/from a socket of the Device.

3.6.

Switch off immediately the Device and unplug the AC/DC adapter if a smoke or unusual smell emanates from the Device.

3.7.

Don't pull out the battery from a battery's box in the Device body. Please approach the Seller or Manufacturer if you need to replace the battery.

3.8.

DON'T DIRECT radiation to the eyes. Eyes shall be protected from falling direct or reflected radiation emitted. The Device shall be only switched on after it is put on the zone to be treated. Medical personnel are recommended to wear goggles while operating the Device to protect against laser emission.

Goggles could not be used when carrying out a single treatment pro- cedure on condition that the Device aperture is tightly pressed to a patient's body.

the treatment is carried out in a patient's face area with the help of light guide nozzles, the goggles are also recommended for the pa- tient.

If

3.9

While treating the apex cardiac beat zone or other cardiac projection, laser radiation of 5 Hz frequency is only permitted to be used.

3.10

Do not get treated or apply treatments to another person if you have

a

pacemaker.

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Operating Manual

3.11.

After completion of a treatment procedure wipe the Device with a wet gauze napkin. Use for this purpose a special cleanser for disinfecting of medical devices. Prevent falling of the cleanser into the Device. The Device cleaning and disinfecting shall be only provided AFTER THE DEVICE IS SWITCHED OFF, and AC/DC adapter is un- plugged.

3.12.

Keep the Device away from children.

3.13

Keep the Device far from the open flame and heat sources and pro- tect it against direct sun light.

3.14

Don't spray flammable matters near the Device.

3.15

The Device disposal shall meet the conventional standards and lo- cal regulations for the environment protection.

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Operating Manual

4. INTENDED USE

4.1. The Device is designed to provide pain relief and also painless, non- invasive, non-pharmacological treatment of diverse diseases of hu- man being.

The Device can be also used in combination with pharmacological methods.

4.2. The Device has three (3) operating modes:

mode 1 laser-phototherapeutic mode QT (use of quantum ther- apy methods)

electrotherapeutic mode - TENS (low frequency electro- neurostimulation)

mode 2

mode 3 combined mode (mode 1 + mode 2).

In mode 1 the Device provides simultaneous penetrative impact of

coherent and incoherent light fluxes of infrared and red spectrum on

the tissues of biological object in combination with a surface impact

provided by a static magnetic field.

In mode 2 the Device provides penetrative impact of low frequency pulse current on the tissues of biological object. In mode 3 the Device provides simultaneous impact by modes 1

and 2.

4.3. The treatment using the Device in mode 1 can be carried out either

by a contact method when the Device is put directly on painful zones

of

or by non-contact method when the Device is at a distance of 0.5-2

cm over wounds, burns, ulcers, etc. of a body surface. In case of

wide injury surface a treatment shall be carried out using scanning

method when the Device is smoothly moved over all the affected ar- ea overlapping 2-4 cm of healthy skin along the edges.

Methodical Recommendations,

The treatment in mode 2 is carried out by a contact method when the Device is put directly on painful zones according to the Methodical Recommendations.

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Operating Manual

4.4. The Device is designed for operation in clinics, hospitals, health care centers and also at home as a family medical device (in accordance with physician's recommendations).

4.5. The Device is designed for indoor operation at ambient temperature in a range from+10 (283-338K) and atmosphere pressure

80%.

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Operating Manual

5. TECHNICAL CHARACTERISTICS *

5.1.

Laser-Phototherapeutic mode:

5.1.1.

Radiation wavelength, nm

- laser radiation

905

- broadband infrared radiation

875

- red radiation

640

5.1.2. Laser and broadband infrared radiation pulse repetition frequency, Hz

- fixed

5, 50, 1000

- variable

250 1

- OFF(see note p.17)

5.1.3. Red radiation pulse repetition frequency, Hz

5.1.4. Radiation aperture, cm 2

5.1.5 Magnetic induction, mT

5.1.6. Laser radiation pulse power, W (no less)

5.1.7. Broadband infrared radiation average power, mW

2

4 0,4

10

30

60

5.1.8.

Treatment time, minutes

1, 2, 5

5.2.

TENS mode:

5.2.1.

Adjustable amplitude of output voltage pulses on metallic electrodes, V

from 0 to 25

5.2.2.

Half-level pulse length at max amplitude, s, no less

20

5.2.3.

Pulse burst frequency, Hz

from 60 to 120

5.3.

Other parameters

5.3.1.

The Device power supply from built-in Li-Ion battery

5.3.2.

- voltage, V

3,7

- capacity

1800 mA hours

Continuous operating time with fully charged battery, hours, no less

8

5.3.3. Battery complete charging time, hours, no more

5.3.4. Input voltage of AC/DC adapter for battery charging 10 40 VAC,

3

50/60 Hz

5.3.5. Output voltage of AC/DC adapter

5.3.6. Overall dimensions, mm

5.3.7. Net weight, g, no more (w/o adapter)

13 VDC

173x55x70

250

5.3.8. Average lifetime, years

5

5.3.9. Laser safety by EN 60825-1

class 1M

5.3.10. Electric safety by EN 60601-1

protection class II type F

*Reference values

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Operating Manual

6. DELIVERY SET

6.1 Delivery set of the Device is presented in Table 1 and Fig. 1.

Table 1

No.

Description

Qty.

1

RIKTA -ESMIL (2A) device with built-in battery

1

2

Protective optical cap

1

3

AC/DC adapter 10 VAC/13 VDC 1.3 A

1

4

Device case

1

5

Packing box

1

6

Operating Manual

1

7

Methodical Recommendations

1

OPTIONS

"KON-1" set of light guide nozzles

"KON-1(1)" light guide nozzle

"KON-2" set of light guide nozzles

"KON-3" set of light guide nozzles

"KON-G" set of light guide nozzles

Goggles

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Operating Manual

Operating Manual Methodical Recommendations Device case and Device with protective optical cap
Operating Manual
Methodical Recommendations
Device case and Device
with protective optical cap

AC/DC adapter

Fig. 1. Delivery set of RIKTA -ESMIL (2A) device

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Operating Manual

7. THE DEVICE DESIGN

7.1

Fig. 2 presents the Device general view.

7.2.

The Device is a stand-alone unit that operates from built-in battery. The Device body is made from durable plastic.

7.3.

The Device is supplied with protective optical cap (11) screwed in its aperture (12) which has double function: protects aperture against external actions (dirt, dust etc.) and allows carrying out cosmetology treatments (e.g. wrinkle effacement).

7.4.

The controls and appropriate light indicators are on the front panel of the Device.

7.5.

On the opposite side of the Device there are metallic electrodes (13) and the radiation aperture (12) to provide impact of electro- magnetic radiation on biological object.

7.6.

Laser and infrared diodes, red LEDs and permanent magnet are mounted inside the Device.

Attention! During the Device operation a human eye is capable to discern radiation of only red LEDs four ruby spots.

DON'T DIRECT radiation to the eyes!

7.7.

The nameplate (see below) is on the Device body:

1 (2A) 13V 1.3A 9 8
1
(2A)
13V
1.3A
9
8

7 6

5 4

2

3

1 AC/DC adapter output voltage and cur-

rent; 3 the Device serial No. and year of manufacture; 4 identification number of EC certification body 5 symbol of electrical safety, protection

class II; 6 symbol of electrical safety, type BF; 7 - Manufacturer's name;

8 - laser hazard, class 1 ; 9 - symbol of laser emission availability

RIKTA -ESMIL (2A)

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Operating Manual

8 9

10

Operating Manual 8 9 10 11 12 13 7 6 5 4 3 14 15 2

11

12

13

7

6
6
Operating Manual 8 9 10 11 12 13 7 6 5 4 3 14 15 2

5

Operating Manual 8 9 10 11 12 13 7 6 5 4 3 14 15 2
Operating Manual 8 9 10 11 12 13 7 6 5 4 3 14 15 2

4

3

Operating Manual 8 9 10 11 12 13 7 6 5 4 3 14 15 2
Operating Manual 8 9 10 11 12 13 7 6 5 4 3 14 15 2

14

15

Operating Manual 8 9 10 11 12 13 7 6 5 4 3 14 15 2

2

Operating Manual 8 9 10 11 12 13 7 6 5 4 3 14 15 2

1

Operating Manual 8 9 10 11 12 13 7 6 5 4 3 14 15 2

Fig. 2. RIKTA -ESMIL (2A) device

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Operating Manual

Legend on Fig. 2:

1.

Socket for connection of AC/DC adapter

2.

Device

3.

Start/Stop button

4

Symbol of laser emission

5

Mode 1 - button "Time": setting treatment time

4.

Mode 2 - button " TENS -": decreasing voltage on electrodes (13)

6

Treatment time LED indicators: "1 min", "2 min", "5 min"

7

"Battery/TENS" indicator - the battery charge / TENS mode

8

Manufacturer's trademark

9

Pulse frequency LED indicators: "5 Hz", "50 Hz", "1000 Hz", "Var"

10

Mode 1 - "Frequency" button: setting pulse repetition frequency

5.

Mode 2 - "+ TENS ": increasing voltage on electrodes (13)

11

Protective optical cap screwed in the Device aperture

12

The Device aperture

13

Electrodes

14

Fixing screw

15

Cover of battery's compartment with battery inside

14 Fixing screw 15 Cover of battery's compartment with battery inside RIKTA -ESMIL (2A) 15
14 Fixing screw 15 Cover of battery's compartment with battery inside RIKTA -ESMIL (2A) 15

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Operating Manual

 

8.

THE DEVICE SETUP

8.1. Take out the Device and accessories from the package. After transportation at low temperature the Device shall be kept at a room temperature of during at least 2 hours.

8.2. Switch on the Device: to do it press "Start/Stop" button (3) and hold it until short sound signal is heard.

 

If after switching on the Device all LED indicators (6) and (9) turn on and steady light, transfer to the Device test (item 8.3).

If after switching on the Device only "1" (6) and "5" (9) LED indica- tors turn on, the Device test is not required and you can start the treatment procedure (items 9.1-9.3).

Repeated test of the device (if necessary) is only possible after the Device is in switched-off state during approximately 45 minutes.

Note

If after switching on the Device or during its operation (including treatment procedure) LED "Battery/TENS" (7) begins blinking red, this means that the battery is discharged and must be recharged to provide the Device opera- tion (see item 9.4).

8.3.

Test the Device in the following sequence:

 

put the Device with an aperture (12) down against any flat light surface (e.g. sheet of white paper or a palm);

shortly press and release "Start/Stop" button (3). You will hear three indicators (9) "100", "50" and "5" will be blinking in turn;

in case if the test is successfully completed in 3-4 sec. you will hear 1 5 ) will light up;

if after the test completion all LED indicators (6), (9) are blink- ing and you hear intermittent sound signal, it means that the Device is failed. In this case unplug the adapter and approach to the Seller that sold you the Device or the Manufacturer.

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9. THE DEVICE OPERATION

The Device has 3 treatment modes:

Mode 1 - LASER-PHOTOTHERAPEUTIC

Mode 2 - TENS

Mode 3 - COMBINED MODE

9.1. Operation in LASER-PHOTOTHERAPEUTIC mode

9.1.1. After the Device is switched on use button "Time" (5) to set the re- quired treatment time (1 min, 2 min or 5 min) in accordance with the "Methodical Recommendations" or physician's prescription. Appropriate LED indicator (6) will turn on (in case if 5 min is select- ed LED indicators "1" and "2" (6) will turn on simultaneously).

Then use "Frequency" button to set the required pulse repetition frequency" 5 Hz or 50 Hz or 1000 Hz or Var (variable). Appropriate LED indicator will turn on. (In case if "Var" frequency is selected LED indicators "50" and "1000" (9) will light up simultaneously).

Note

OFF - to use TENS mode, press in series "Frequency" button (10) until no one of LED indicators (9) lights up.

9.1.2. If the protective optical cap is not used when treating, unscrew it (turn counter-clockwise) and put in safe place.

9.1.3. Put the Device aperture (12) on a patient's body zone to be treated and press "Start/Stop" button (3). You will hear "beep" and LED in- dicator(s) (6) corresponding to the selected treatment time will be blinking. It means that the treatment procedure began.

During the treatment procedure the Device provides a time count down: indicators (6) are blinking in turn indicating remaining time.

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Operating Manual

On the termination of treatment time you will hear "beep" again, light emission is turned off and one of indicators (6) corresponding to the preset treatment time will steadily light.

9.1.4. At any time you can interrupt a treatment procedure by pressing "Start/Stop" button (3). If you press the button again, the treatment procedure begins again.

9.1.5. To switch off the Device, press "Start/Stop" button (3) and hold it during 2-3 seconds; you will hear "beep", all LED indicators will go out and the Device will be switched off.

Note

If switch-on Device is not used during 40 seconds (no one of buttons is pressed and treatment procedure is not carried out), then "beep" sounds and the Device is automatically switched off.

9.2. Operation in TENS mode

9.2.1. Device has been described in item 8.2.

9.2.2. To provide operation in TENS mode (mode 2) the mode 1 must be cut off. To do it, press successively "Frequency" button (10) until no one of LED indicators (9) lights up.

9.2.3. Then use "Time" button (5) to set the required treatment time (see item 9.1.1).

9.2.4. Initially voltage on the electrodes (13) is not available and "Battery/TENS" indicator (7) is turned off. Press "+ TENS" button, "Battery/TENS" indicator (7) will light alternately red and green. It means that the TENS mode is activated.

9.2.5. While operating in TENS mode, please, remember the following:

as

voltage is only fed on the electrodes (13) when the electrodes are in contact with the patient's skin; when transferring the treatment from previous zone to next zone, voltage level is kept the same as for the previous zone; voltage level is set on the basis of personal sensation of a pa- tient.

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9.2.6. Put the Device with aperture (12) down on a zone of treatment. After the electrodes (13) are in contact with the patient's skin, a "beep" will sound and LED indicator "Battery/TENS" (7) will be blinking green.

9.2.7. Press successively "+ TENS" button (10) to adjust voltage to the level required for treatment (basing on personal sensation of a pa- tient) and begin treatment procedure.

Please remember, that:

each short press of "TENS -" button (5) leads to decrease of voltage on the electrodes (13); each short press of "+ TENS" button (10) leads to increase of voltage on the electrodes (13); in case of prolonged pressing of one of the buttons, voltage level changes quickly; voltage on the electrodes is in direct proportion to blinking fre- quency of "Battery/TENS" indicator (7) - the higher blinking frequency, the higher voltage.

9.2.8. At the beginning of impact of electric stimulating pulses, the state of the electrodes will be changing and "Battery/TENS" light indicator (7) will be blinking green. After a while, the skin state is stabilized and the indicator (7) begins blink- ing red.

9.2.9. When the Device is moved to a new zone or in case of failure of the contact between the electrodes and skin, a "beep" sounds and "Battery/TENS" light indicator (7) begins to light alternatively red and green. After the contact with skin at a new zone is provided, voltage will be supplied to the electrodes and the indicator (7) will be blinking green.

9.2.10. The treatment procedure duration is defined by the time which is set by item 9.2.2. On the termination of procedure time, voltage on the electrodes (13) will equal zero (0).

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Operating Manual

9.3. Operation in COMBINED mode

9.3.1. In this mode simultaneous impact of therapeutic factors described in item 4.2 of the Operating Manual is available.

9.3.2. Switch on the Device by pressing Start/Stop button (3) as has been described in item 8.2 and then prepare the Device for operation, performing actions described in items 9.1.1-9.1.2.

9.3.3. Put the Device aperture (12) and press "Start/Stop" button (3). "Beep" will sound and indicator(s) (6) corresponding to the selected treatment time will be blinking.

9.3.4. To activate TENS mode after pressing "Start/Stop" button (3) and providing contact of the electrodes (13) with skin, press successive- ly "+ TENS " button (10) to adjust comfortable voltage level (basing on your own sensation).

After providing electrodes contact with skin, "Battery/TENS" indica- tor (7) starts blinking green and after the stabilization of skin state between the electrodes it begins blinking red.

9.3.5. On the termination of the set time of treatment procedure, voltage on the electrodes (13) equals zero (0).

Note

As in TENS mode (mode 2), in case of failure of a contact between the electrodes and skin, a "beep" sounds and "Battery/TENS" indicator (7) be- gins blinking in turn red and green. To continue the procedure, it is neces- sary to provide contact with skin.

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9.4. Battery charge monitoring

9.4.1. The battery is in a battery's box (15) in the Device body. The bat- tery charge is automatically checked after the Device is switched on and during the Device operation.

9.4.2. The battery can be charged in any state of the Device. To charge the battery, the Device shall be connected to main power through AC/DC adapter.

9.4.3. To charge the battery:

- connect AC/DC adapter connection cable to the socket (1) of the Device;

- plug AC/DC adapter in a wall outlet. Approximate time of the battery charging - no more than 3 hours (depending on the battery condition). After the charging process is completed (in- dicator "Battery/TENS" will light green), unplug AC/DC adaptor from wall outlet and disconnect the adapter connection cable from the Device socket. The Device is ready to work stand alone.

9.4.4. Please remember that light indicator "Battery/TENS" (7) has two functions:

before beginning treatment procedure (before pressing "Start/Stop" button (3)) this indicator is used for indication of the battery charge condition; during the treatment (after pressing "Start/Stop" button (3)) this indicator is used for indication of normal operation in TENS mode.

9.4.5. If the battery voltage is normal, the "Battery/TENS" indicator is off. This means that the battery is charged and the Device is ready to work. If the battery voltage is less than the minimum allowable level, the "Battery/TENS" indicator will be blinking red. This means that the battery charge is only enough for the Device operation during ap- proximately 10 minutes. In case of continuation of the Device oper- ation the battery will be yet more discharged, the Device will gener- ate a short intermittent signal and then will be switched off. All indi- cators will be out. Therefore, it is necessary to charge the battery to provide the Device normal work.

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Operating Manual

 
 

10.

MAINTENANCE

 

10.1. To provide reliable operation of the Device the User has to carry out in time its maintenance in accordance with Table 2 of the Man- ual.

10.2. During the maintenance strictly follow safety precautions by section 3 of the Manual.

10.3. If during the maintenance you will find out that the Device doesn't meet any technical requirements stated in Table 2, further opera- tion of the Device is prohibited and it is subject to repair.

 

Table 2

Periodicity

Work description

Technical requirements

Before

each

Visual inspection of the Device w/o any special instrument.

Absence of mechanical defects on the Device and AC/DC adapter

treatment

Check the following:

1. Battery charge

using

"Battery/TENS" indicator (7) shall not light up.

"Battery/TENS" (7) indicator.

2. Availability of radiations.

After the Device aperture (12) is put on a zone of treatment and "Start/Stop" button (3) is pressed, red radiation shall be visible.

3. Disinfection (if necessary).

In accordance with item 3.11 of the Manual.

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Operating Manual

 
 

11.

TROUBLESHOOTING

 

11.1.

Possible failures of the Device, their causes and appropriate cor- rective measures are listed in Table 3.

 

3

 

Failure

Possible causes

Corrective measures

Power is on but LED indicators (6) and (9) don't light up.

The battery is fully dis- charged or the Device failure.

Charge the battery (item 9.4).

If after the battery charging LED indicators (6) and (9) don't light up when the Device is switched on, the Device is subject to repair by Manufac- turer.

When the Device is switched on and but- tons "Time" (5) and "Frequency" (10) are pressed, any of indica- tors (6), (9) doesn't light up.

Failure of the Device.

The Device repair by Manufac- turer.

When testing the De- vice (item 8.3) LED indicators (6), (9) light intermittently and you hear intermittent sound signal.

One

or more kinds of

The Device repair by Manufac- turer.

radiation is

(are) not

available.

 
 

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Operating Manual

12. PACKING, STORAGE AND TRANSPORTATION

12.1. Each Device is supplied with protective optical cap (11) screwed in the aperture and is placed in a special case. The case with the De- vice inside is placed together with accessories in the Manufactur- er's package.

12.2. The Device shall be stored in the Manufacturer's package in the o C (283-308K) and relative humidity of no more than 80% (at +25 o C). The storage room shall be free of dust, mercury vapor, acids and alkalis provoking corrosion.

12.3. The Device can be transported by all kinds of enclosed transport while packed in the Manufacturer's transportation package. The package shall be in a stable position without any movements during the transportation.

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13. MANUFACTURER'S WARRANTY

13.1. Manufacturer warrants the Device against defects in material and workmanship under normal use, service, storage and transportation for a period of twelve (12) months from the date of original selling of the Device. Within the aforesaid period the Manufacturer shall pro- vide free of charge repair of the Device.

13.2. This warranty will be granted only upon presentation of this Operat- ing Manual containing a warranty card with the Device type, serial number, date of sale, Seller's name and stamp.

13.3. This warranty does not apply to any of the following:

damage caused by accidents including, but not limited to, lightning, fire, water; mechanical damage including the damage during transporta- tion; damage to the Device resulting from neglect and/or misuse in- cluding but not limited to, failure to use, repair and/or applica- tion of the Device for its normal purposes and/or in accord- ance with the operating instructions on its proper use; damage resulting from falling of foreign matters (such as nails, coins, hairpin etc.) into the Device; modification or repair of the Device during the warranty period by unauthorized persons or organizations; removing seals from the Device.

13.4. On the expiry of warranty period the Device repair shall be made at the expense of the user.

13.5. In case if the date of sale a in the warranty card, the warranty period is counted off from the date of the Device manufacture.

13.6. If you need service, whether or not under warranty, please ap- proach the Seller who sold you the Device. Should you have any questions which the Seller is unable to an- swer, please contact the Manufacturer.

RIKTA -ESMIL (2A)

25

 

Operating Manual

 

14.

ACCEPTANCE CERTIFICATE

14.1

RIKTA -ESMIL (2A) device, serial No

meets

the Manufacturer's technical specifications and is declared good for

operation.

Date of manufacture

 

Signature of the person responsible for acceptance

Stamp

26

RIKTA -ESMIL (2A)

Operating Manual

WARRANTY CARD Warranty peri- Device RIKTA -ESMIL (2A) od Serial No. Date of sale Seller's
WARRANTY CARD
Warranty peri-
Device
RIKTA -ESMIL (2A)
od
Serial No.
Date of sale
Seller's Name
Seller's Address
Seller's phone and fax
Seller's stamp

Manufacturer:

151 Liublinskaya St. 109341 Moscow, Russia JSC "MILTA Humanitarian-Information Technologies Design & Production Company" (MILTA PKP GIT)

Tel.: +7(495)228-1433

Fax: +7(495) 346-9247

Web site: www.quantnmed.ru EU-Representative: gasteiger science GmbH Dietmar Schaffarczyk Gollierstrasse 19, D-80339 M nchen, Germany Phone: +49 (0) 160 780 96 28 Fax: +49 (0) 3212 36 99 590 Mail: zyk@gasteiger-science.com

RIKTA -ESMIL (2A)

27