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AUTHORIZATION
NAME TITLE SIGNATURE DATE
Issued Ofer Adi Service support 12 May 09
by:
Reviewed Omri Kesler COO 12 May 09
By:
Approved Danny Erez CEO 12 May 09
By:

Revision History

REV DESCRIPTION NAME DATE

A First Issue Ofer Adi 12 May 09


B First Issue Ofer Adi 5 Aug. 09
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Service Manual
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Copyright © 2009 Viora Ltd. All rights reserved.


Viora Ltd. reserves the right to make changes to its products or specifications to improve performance,
reliability, or manufacturability. Information furnished by Viora Ltd. is believed to be accurate and reliable.
However, Viora Ltd. assumes no responsibility for its use. No license is granted by its implication or
otherwise under any patent or patent rights of Viora Ltd.
No part of this document may be produced or transmitted in any form or by any means, electronic or
mechanical, for any purpose, without the express written permission of Viora Ltd.
Data is subject to change without notification.
Viora Ltd. has patents and pending patent applications, trademarks, copyrights, or other intellectual
property rights covering subject matter in this document. The furnishing of this document does not give
you any license to these patents, trademarks, copyrights, or other intellectual property rights except as
expressly provided in any written agreement from Viora Ltd.
Specifications are subject to change without notice.

Release Date: May 2009

 Before using the device, please check local regulations. If any local
legislation is violated, use cannot be authorized.
 In the United States, federal law restricts prescription medical devices to
sale by or on the order of a physician, or properly licensed practitioner.
Viora makes no representations regarding federal, state, or local laws or
regulations that might apply to the use and operation of this device.

Corporate Headquarters
Viora, Inc.
30 Montgomery Street
Suite 660
Jersey City, NJ USA 07302
Tel: +1 201 332 4100
Fax: + 1 201 332 4200
Website:www.vioramed.com
E-mail: info@vioramed.com

0344
This device complies with the European Medical Device Directive 93/42/EEC
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Table of Content
1 Background ...................................................................................................................5
2 Scope ............................................................................................................................5
3 Applicable Documents ................................................................................................5
4 Responsibilities: ............................................................................................................5
5 Before You Start ............................................................................................................6
5.1 Conventions Used in this Manual….................................. ............................................6
5.2 Explanation of the Symbols Used in the System…………......................... ..................7
6 Introduction....................................................................................................................8
6.1 System Overview............................. .............................................................................8
6.2 Console.............................. ...........................................................................................8
6.2.1 Display Screen and Keypad…………………........................................... ...... ..............9
6.2.2 System View - Left Side..............................................................................................10
6.2.3 System View - Right Side.............................................................. .............................10
6.2.4 Rear Side............................................................ ........................................................11
6.3 Hand piece.............................. ..................................................................... ..............12
6.4 Technical Specifications.................................... .........................................................13
7 Safety. .........................................................................................................................14
7.1 Introduction……….................. ....................................................................................14
7.2 Installing the System……....................... .....................................................................14
7.3 Operating the System............................. ...................................................................14
7.4 Fire Hazards.............................. .................................................................................15
7.5 System Classifications............................... .................................................................15
7.6 Moving the System within the Facility………......................... .....................................15
7.7 Electrical Requirements................................ ..............................................................15
7.8 Maintaining the System…………......................... .......................................................16
7.9 Environmental Requirements.................................... .................................................16
7.9.1 Air Quality............................................................... ....................................................17
7.9.2 Space Requirements............................................................... ...................................17
8 System Operation……… .............................................................................................17
8.1.1 Language Set Up.............................................................. ..........................................17
8.1.2 Display Brightness Set Up.................................................................... ......................18
8.1.3 Delay for Handle Cooling Set Up…………................................................... ..............19
8.2 System Test Procedures.............................................................................................19
1.2.1 Basic Preparation...................................................................... .................................19
8.2.2 System Fans Test.............................................................. .........................................19
8.2.3 Energy Calibration procedure……........................................................ .....................20
8.3 Replacing the Hand Piece............................... ...........................................................22
8.4 Maintenance............................... ................................................................................24
9 Replacing Parts ...........................................................................................................26
9.1.1 Fuse Replacement......................................................................................................26
9.1.2 Replacing Main Board.............................................................. ..................................30
9.1.3 Replacing Display Board…………………............................................. ......................33
9.1.4 Touch Panel (Lexan) Assembly................................................................. .................34
Appendix....................... ..............................................................................................................35
Troubleshooting Diagram............................................................................................................35
Service Kit ....................................................................................................................................44
Electrical drew of the system:......................................................................................................44
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1 Background
This Service Manual is part of the Service and Maintenance Plan for the Trios™
system.

2 Scope
This document applies to Service and Maintenance. It defines the service
procedures for the Trios™ system.

3 Applicable Documents
N/A

4 Responsibilities:
Service department

Engineering Manager – Update this document

QA&RA Manager – Documenting


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5 Before You Start

Warning
 Read this manual to become familiar with all safety requirements
and operating procedures before attempting to operate the system.
 Any intense optical energy device can cause injury if used
improperly.
 High voltage is present inside the system. Always be aware of the
possible dangers and take proper safeguards as described in this
manual.
 The Trios™ system must be serviced only by qualified personnel.

5.1 Conventions Used in this Manual

The following conventions in the form of notes, cautions and warnings are
used in this manual:

Note
The content of this Note offers general information that is important to
keep in mind.

Caution
A Caution alerts the user to the possibility of a problem with the device
associated with its use or misuse. Such problems include system
malfunction, failure, and damage to the system or other property. The
caution statement includes a precautionary action that should be taken to
avoid the hazard.

Warning
A Warning alerts the user to the possibility of injury, death, or serious
adverse Trios associated with the use or misuse of the system.
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5.2 Explanation of the Symbols Used in the System

Symbol Description

Attention: Consult Accompanying Document

CE Compliance Symbol
0344

CSA Compliance Symbol

Dispose of according to WEEE regulations

Fuse

Type BF Equipment

Manufacturer

Non-ionizing electromagnetic radiation


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6 Introduction
The use of TriosTM in aesthetic applications is based on the principle of Selective
Photothermolysis. According to this principle, pulsed light parameters (wavelength,
pulse duration and energy fluency) are chosen to selectively target light sensitive
cells while minimizing damage to surrounding tissues.

The system is continuously monitored and controlled by an internal computer and it


utilizes a self-inspection mechanism to verify and follow the input of each lamp,
assuring and maintaining treatment integrity from the first to last pulse. The easy
modular design allows for quick adjustments and replacement of disposable lamp.

The system features three specially designed hand pieces for the top three
phototherapy applications; hair removal, acne treatments and the treatment of
vascular and pigmented lesions (skin rejuvenation).

The Trios™ system is CE certified; FDA approved, and complies with CSA
Canadian regulations. While this system is considered safe for both the operator
and the patient, it should be operated only by trained, qualified treating attendants.

6.1 System Overview

The system includes four core modules: the Console, the Hair Removal (HR) hand
piece, Acne Clearance (AC) hand piece and Skin Rejuvenation (SR) hand piece.

6.2 Console

Figure 1 Main Consol


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6.2.1 Display Screen and Keypad

Figure 2 Display screen and keypad.


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6.2.2 System View - Left Side

Figure 3. system views - left side.

6.2.3 System View - Right Side

Figure 4. System View - Right Side.


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6.2.4 Rear Side

Software
p lu g

On/Off buzzer
switch

Figure 5. System View – Rear Side.


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6.2.5 Hand piece


The hand piece (Figure 6) houses the mechanism which generates the light
pulse. The optical treatment head is connected to the system console by an
umbilicus cord containing electrical wiring. Light from a Xenon flash lamp is
directed through a long-pass optical filter and focused into a transparent light
guide (Figure 7) that is placed in contact with the skin.

The spot size of the light on the skin is 15mm x 50mm which defines the footprint
of each treatment pulse. The light pulse is activated by pressing the activation
button on the hand piece.

Activation button

Figure 6. Hand Piece.

Figure 7. Light Guide.


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When not in operation, place the hand piece in its cradle on the side of the
system.

The system is supplied with one hand piece, optimized for photoepilation. Two
additional hand pieces are available for purchase, depending on the clinic's
needs.

The hand pieces are equipped with optimal filters for the following applications
(specified in nano meter):

 Hair Removal – 530 – 1,200nm


 Skin Rejuvenation (Vascular & Pigmented lesions) – 570 – 1,200nm
 Acne Clearance – 400 – 1,200nm

Note
The system automatically recognizes the hand piece and filter connected.

6.3 Technical Specifications


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7 Safety
This chapter describes the safety issues regarding the use and maintenance of the Trios™
system, with special emphasis on optical and electrical safety.

7.1 Introduction
The system is designed for safe and reliable treatment, when used in accordance with
proper operation and maintenance procedures. Only trained practitioners are qualified to
operate the system. The user and all other personnel operating or maintaining the system
should be familiar with the safety information provided in this chapter. Viora Ltd. assumes
no liability whatsoever for any damage or injury as a result of an application of a product
which is not in strict accordance with the instructions provided with the product. The
primary consideration should be to maximize safety for both treating attendant and the
patient.

Warning
 Read this chapter to be familiar with all of its safety requirements and
operating procedures prior to operating the system.
 Any intense optical energy can cause injury if used improperly.
 High voltage is present inside the system.
 Always be aware of the possible dangers and take proper safeguards
as described in this manual.
 For complete contact information please refer to page 3 of this
manual.

7.2 Installing the System


When installing the system, ensure that the system is grounded through the grounding
conductor in the power cable. This protective grounding is essential for safe operation.

7.3 Operating the System


 Keep system cover closed. Do not remove or t touch any of the system's inner
components.

Warning
Always turn the system off before connecting or disconnecting the
applicator!
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 Keep your hands away from the hand piece during system start-up.

 Keep the hand piece dry and clean.

 Do not allow the hand piece to come in contact with hard materials, excessive heat
or humidity; these may damage the hand piece.

 Never use the system in the presence of explosive or flammable materials.

 Make sure that all treatment personnel are familiar with the system's controls and
know how to shut down the system instantly.

7.4 Fire Hazards


 The absorption of optical energy raises the temperature of the absorbing material.
Do not use the system in the presence of explosive or flammable materials.

 Do not use flammable substances when preparing the skin for treatment.

 If alcohol is used for disinfecting, it must be allowed to dry thoroughly before the
system is used.

7.5 System Classifications


 Electric shock protection: Class I, Type BF

 Protection against ingress of liquids: Ordinary equipment

 Not suitable for use in presence of flammable substances

 The Trios™ system and applicators comply with U.S. Federal Regulations.

 The system is classified as a Class IIb device, in accordance with the standards set
by the European Medical Device Directive (93/42/EEC) for CE marking.

7.6 Moving the System within the Facility


To move the system within the facility:
 Properly shut down the system.
 Disconnect the power cable.
 Secure the treatment head in the cradle.
 Carefully carry the system to its location.

If the TriosTM has to be moved to another location, it is advised to pack it in its original
package.

7.7 Electrical Requirements


The system is preset at the factory to accommodate the local line voltage according to the
customer's order. Accordingly, the system will require a separate line supply of one of the
following (appropriate to your country):
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 115 VAC; 6.3A; 50-60 Hz, single phase


 230 VAC; 3.15A; 50 Hz; single phase

Warning
 For continued protection against fire, replace the fuse only with one of
the same type and rating.
 Proper grounding is essential for safe operation.

The system is grounded through the grounding conductor (yellow/green) in the power
cable which is plugged into the network electricity outlet. Suitable and appropriate
grounding is essential for safe operation.

Input power lines should be free of transients, voltage and current spikes, sags and
surges. Consequently the system power line should not be shared with other heavy
variable loads such as elevators, air conditioning systems, large motors etc. Viora
strongly recommends that the system be connected to a separate power line with
separate circuit breakers.

The main fuse, located within the unit, is a 3.15A circuit breaker (for 230V) or 6.3A (for
115V).

Power supply to the system will cease when the circuit breaker trips.

Caution
Verify that the Trios TM is wired to the appropriate line voltage of your
country (115 V or 230V).

7.8 Maintaining the System


 Only authorized technicians are qualified to service the system.

 Shut down the system and disconnect the power cable before performing any
maintenance procedures.

7.9 Environmental Requirements


 Corrosive materials can damage electronic parts; therefore the system should
operate in a non-corrosive atmosphere.

 Metallic dust can damage electrical equipment. Dust particles absorb light and heat
up. Hot particles located on the optical light guide can damage it; therefore dust
particles should be kept to a minimum.
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 For optimal operation of the system, maintain room temperature between 10º - 30ºC
(50º-86ºF) and relative humidity of less than 80%.

 If the system has been stored in an environment cooler than the above mentioned
temperatures, allow it time to warm up to room temperature before first activation.

7.9.1 Air Quality

The system should operate in a non-corrosive atmosphere. Corrosive materials, such as


acids, can damage electrical wiring, electronic components and the surfaces of optical
components. Air-borne dust particles should be kept to a minimum as they absorb light
and heat up.

Place the Trios™ system away from heating ducts or other outlets.

7.9.2 Space Requirements

Trios TM is designed for installation in a clinical environment and requires minimal site
preparation. The base dimensions of the system are 45 cm (L) X 38 cm (W) X 27 cm (H).
A sufficient space of 10cm should be cleared at the back of the device to permit
appropriate ventilation.

8 System Operation
In this section you will find set up and operational instructions for the Trios™ system as well as
test procedures and maintenance requirements.

Use of controls, adjustments or performance of procedures other than those specified herein
may result in hazardous light exposure

8.1.1 Language Set Up

• Disconnect the hand piece.

• Turn the system On.

• Simultaneously press the left and right arrows for approximately 5 seconds for the
language options to appear on the screen (Figure 8).
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Figure 8. Language Set Up.

• Make your selection using the up and down navigation arrows.

• Press OK.

• Turn the system Off before reconnecting the hand piece.

8.1.2 Display Contrast Set Up

• Disconnect the hand piece

• Turn the system On

• Press OK for approximately 10 second for the brightness options to appear on the
screen (Figure 9)

Figure 9. Display Brightness Set Up.


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• Make your selection using the Left and right navigation arrows.

• Pres the down arrow to return to the operate screen.

• Turn the system Off before reconnecting the hand piece.

8.1.3 Delay for Handle Cooling Set Up

• Disconnect the hand piece.


• Turn the system On
• Simultaneously press the left and down arrows for approximately 10 seconds for
The delay options will appear on the screen (Figure 10)

Figure 10. Delay for Handle Cooling Set Up.

• Make your selection using the Left and right navigation arrows.
• Press OK.
• Turn the system Off before reconnecting the hand piece.

8.2 System Test Procedures

8.2.1 Basic Preparation

1. Install the Hair Removal (HR) applicator.


2. Plug in the power cord and turn the system ON.

8.2.2 System Fans Test

• When the system is turned on, the fans will start to operate automatically, Proper
air flow is conducted from the outside into the system to both fans.

Warning
 Check for dust or any obstacle on the finger guard of the fan and
carefully clean, if required.
 Proper air flow is essential for safe operation.
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8.2.3 Energy Calibration procedure

Note
Energy calibration procedure is essential for an appropriate functionality
of the system.
Calibration procedure should be made with HR applicator.
This procedure must be executed annually.
The calibration procedure can be divided into 3 phases:
1. System Set Up
2. Measurement Equipment Set Up
3. Calibration Measurements and Adjustments
Below you will find detailed instructions to all 3 phases.
System Set Up

 Turn the machine ON.


 Define the treatment parameters as Light Skin, Light Hair. Use the Up or down key to
move between the fields and then press the O.K key in order to chose your selection.
(Figures 11,12)

Figure 11. Selecting Skin Type.

Figure 12. Selecting Hair Type.

 Define the treatment intensity to level 15 by pressing the right arrow key, and then press
the Press Operate key.
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Measurement Equipment Set Up

 Adjust the range of the power meter RANGE to be – 300 Joules.


 Adjust the Laser field to be – AIR (Figure 13).

Figure 13. Equipment Set up.

Calibration Measurements and Adjustments


 Place the light output of the handle over a Laser Power meter and Press the trigger on
the hand piece in order to emit a pulse (Figure 14).

Figure 14. Lamp energy measurement with a laser power meter.

 At this stage the power to be read will be 165 Joules (+-5%).


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 In case the output is not 165 Joules, either reduce or increase the system
capacitors' charging, by means of the potentiometer VR1 (installed on the main
board card) (Figure 15).

Figure 15. Location of Potentiometer VR1.

 Define a new measurement and check accordingly.

Turning clockwise will decrease the power output.

Make sure not to release more than 8 consecutive pulses before letting the system to
cool down to avoid inaccuracies in the read.

To calculate the Total Power use the below formula:


 The maximum output required is: 22J/Cm2.
 The area of the light power output is: 15 [mm] X 50 [mm] = 7,5 [Cm2]
 Total Power use the below formula: [J/Cm2] X 7.5 [Cm2] = [J]

8.3 Replacing the Hand Piece

The TriosTM system is equipped with an internal computer and counter which constantly
test the hand piece attached to ensure its efficacy and helps maintain Viora's high
standards of treatment and treatment's safety.

When the hand piece has completed its designated number of pulses, the system will
alert the operator to replace the hand piece.
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8.3.1 Hand piece replacement will be required in the following situations:

 To utilize a different application (each application has its own unique hand
piece).
 When the system detects a significant drop in energy level.
 When significant contamination has been accumulated on the surface of
the light guide. (You may avoid this situation by simply cleaning the hand
piece after each treatment using humid duster).
 When physical damage has been inflicted on the light guide or the hand
piece casing.
 When the hand piece achieved 100,000 pulses.

8.3.2 Replacing Hand Piece

To replace the hand piece, follow the below procedure:

• Make sure the system is turned Off.

• Disconnect the hand piece from the back of the main console by pulling the
connector's bridge until the safety pin enters the designed niche (Figures 16)

Safety pin

Figures 16. releasing the hand piece from the system's connector.
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• When the connector's bridge stops on the improved safety pin push the safety
pin with any object that has diameter smaller than 3 mm.(Figure 17)

Figure 17. Relicing the safety pin.

• While holding the safety pin down keep pushing the connector's bridge forward
until the outlet is released.

• Connect the new selected hand piece to its port on the rear panel.

• Contact your distributor regarding disposal or replacement of the used hand


piece.

8.4 Maintenance

While the Trios™ system should not be serviced by anyone other than an authorized agent or
technician, the system requires minimal preventative maintenance and cleaning to ensure
optimal system performance.

Warning

The symbol located near the power cable's connection port


indicates:
WARNING! DISCONNECT POWER SUPPLY CABLE BEFORE
MAINTENANCE OR SERVICE PROCEDURES TO AVOID
ELECTRIC SHOCK.
For continued protection against fire, replace the fuse only with one of
the same type and rating.
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 Only authorized technicians are qualified to service the system.

 Shut down the system and disconnect the power cable before performing any maintenance
procedures.

8.4.1 Cloning the air filter

 it is essential to clean the system's air filter every two years:

o Remove the system cover.

o Remove the air filter's cover and expose the air filter (fig18- 20)

o Cline the filter with soap water (fig 21)

o Dry the filter from water remains.

o Reverse the above steps, and continue working with the system

Figure 18 Figure 19 Figure 20

Figure 21
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9 Replacing Parts
9.1.1 Triac Replacing

 Disconnect the Triac electrical wires.

 Unscrew two M4 bolts, holding the Triac to the Transformator.

 Replace the Triac and tight back the M4 bolts.

 Reconnect the electrical wires as follows (figure 22):

Figure 22 Triac wiring.


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9.1.2 Connector replacing

 Disconnect the high voltage connections (figure 23,)

Figure 23 high voltage connections

 Disconnect the air pipe from the fast connection (figure 24).

 Disconnect the
40A wires from
the RF Chock and
from the main
capacitors(figure
25)

Figure 25 RF Chock and capacitors.

 Disconnect the D- Type harness from the display board.


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 Unscrew the nuts, tighten the diodes to the system body (Figure 26)

Figure 26 diodes'' tighten nuts

 Unscrew two nut, holding the connector to the system body, from the internal side of the
system and another Allen bolt from the external side (use 12mm key and Allen 4mm key
see figure 27 ,28).

Figure 27, 28 Connector's bolt and nuts

 Replace the connector and reassemble it by reversing the above process.


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9.1.3 Fuse Replacement

 Gently press on the two clips on both side of the fuse hose, and pull (Figure 29).

Figure 29. Fuse house and clips.

 Replace the blown fuse with a new one (Figure 30).

Figure 30. Replacing the fuse.


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9.1.4 Replacing internal fuses

 The Trios system contain 4 protection fuses except to the main one (that locate on the
rear side of the system) in order to replace the fuses please follow the below steps.

 Locket the blown fuse according to the type of the malfunction (Figure 31).

Figure 31 fuses location.

- Fuse F1 @ 4A.

- Fuse F2 @ 0.032A.

- Fuse F3 @ 0.5A (for 220V) and 0.1A (for 110V).

- Fuse F4 @ 3.15A (for220V) and 6.3 (for 110V).

 Open the fuse hose cover by turn it counterclockwise.

 Replace the fuse and close the fuse hose.


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9.1.5 Replacing Main Board

 Disconnect the transformer from the machine's base by unscrewing four M4 bolts.
Moving the transformer will create a working space and access to the main board
(Figure 32).

Four M4 bolts

Figure 32. Replacing Main Board

 Disconnect the relevant harnesses from the main board (Figures 33-37).

Note
You may want to consider marking the harnesses before you disconnect
the main board. It will make the reconnection of the harness easier.

Connectors J1, J2

Figure 33. Connections J1, J2.


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Fans' Harnesses

Figure 34. Funs Connections.

Display Harness

Figure 35. Display Harness

Connector J 4
High voltage connection

Figure 36 Connector J4 and High voltage connection


.

 Disconnect the main board from the machine's body by unscrewing five of
the Allen M4 bolts (use Ball End T-Handle - Inch).

 Replace the malfunction board with a new board.


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Caution
Always check for the QC sticker on the board! This sticker approves that
the board has past a successful calibration (Figure 37).

QC Sticker

Figure 37. Q.C sticker location.

 Reconnect the harnesses.


 Reconnect the transformer.
 Gently replace the machine cover.
 Connect the machine to the electricity network.
 Test the machine for pulses.

9.1.6 Replacing Display Board

 Disconnect the harnesses from the PLC (Figure 38).


 Disconnect the display board from the cover by unscrewing two M4X8
bolts.
 Replace the board.
 Connect the display board to the cover by screwing two M4X8 bolts.
 Confirm that all of the display's LEDs are sitting in place.
 Connect the harness HRVio-10000 from j3 (on the display board) to the in
put of the PLC, and harness HRVio-10003from j2 (on the display board) to
the out put of the PLC.
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 Make sure that all of the harnesses are properly connected (Figure 26 ).

HRVio-1000
PLC OUT PUT
Display board

HRVio-10003 PLC in put

Figure 38. Display and PLC Harnesses.

9.1.7 Replacing Touch Panel (Lexan)

 Disconnect the Lexan harness from the display board.


 Peel the Lexanfrom the system cover.
 Clean the cover using a dry cloth and make sure the lexan area is dry.
 Slide the lexan's harness in to the designated notch on the cover.
 Connect the harness to jp1 on the display board (Figure 39).

Lexan's harness

Designated notch
Jp1 connection

Figure 39. Connection JP1 location.


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Appendix

Appendix A

Troubleshooting

Note
The Troubleshooting chapter is presented as a process. The colored
block diagram represents symptom (Blue), possible cause (Yellow) and
solution (Green).
All of Viora's products are based on replacing sub-system principals.
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Appendix B
Service Kit

TRIOS™ Service Kit


P/N: VTR-0014-220 VTR-0014-110

# Item Description Part Number QTY Image


1 IPL Display board 2

AssVIO-3000
2 IPL Main board 2

AssVIO-2023
3 Fuses 5X20 3.15A /6.3 VIO- 2019-3.15 10
S-B

4 Fuses 5X20 0.032A S-B VIO-2021-F2 10

5 Fuses 5X20 4A S-B VIO-2021-F1 10

6 Fuses 5X20 0.5A / 1.5 Vio-2021-F3 10


A S-B

7 Fuses 5X20 2.5A / 5 A Vio-2021-F4 10


S-B

8 Lexan VIO-2025 2
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9 Vio-2007 2

Triac 600 V 40 A
NTE5679
10 Rectifier bridge 800V Vio2008 2
25A

11 Vio-1014 2

Capacitor 27,000mF
,250 V
12 Fan 12V VIO-2012 2

13 Line filter VIO-2019 2

14 Vio-2014 2

Diode D2
15 Pump 220V/110 AC0602-220/ 2
AC0602-110

16 Vio-2013-2 2

Emergency Stop Switch


17 VIO-7010 2

Buzzer Switch
17 VIO-7010-1 2

Buzzer Switch old


version
18 Power Cable VTR3001-EU 2
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19 PLC VIO-2028 1

Appendix B
Electrical drew of the system:

Appendix C
IPL Pulse Test Of the Trios™

Dear colleague, in order to verify proper pulse of the Trios™, please follow the below procedure
step by step test.

1. Overview
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This procedure is indicated to verify proper IPL pulse of the Trios™ , and proper
indication by 'ready light' and sound.

2. Required tools

2.1. Volt meter

2.2. Philips head Screwdriver

Warning!
During the test procedure you will be asked to measure high voltage, if you not an authoritative
technician, that train by Viora Ltd, and used with the proper tools, you not allowed to perform
this test!

3. Procedure
3.1. Internal part access
3.1.1. Open the system's cover by unscrewing the two M4 bolts located in the rear side
of the system and the other 6 M4 bolts located in the bottom of the system (Figure

1 & 2).
Figure 1 & 2. M4 bolts location

4. Capacitors' charging & harnesses test procedure


4.1. Turn the system ON.
4.2. Set the program for 'light skin', 'light hair'; treatment intensity level 15.
4.3. Measure the voltage on the capacitors (Figure 3) and verify that it between 105V and
195V.
 If the Voltage on the capacitors is more than 195V, there is a possibility of system
overcharge requiring the replacement of the Tryac (Figure 4).
 If the Voltage on the capacitors is less than 105V, there is a possibility of power
board failure, requiring the replacement of the power board (figure 5).
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Figure 3. Figure 4. Figure 5.

 If the voltage values are correct, continue with the test procedure.

4.4. Verify minimum 350V between the capacitors cathode to the anode on the D2 diode
(Figure 6 & 7).
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Figure 6 & 7. Measurement's point

Please note the measurement should be performed exactly on the indicated locations.

 If the voltage value is below 350V (~180V), check for short circuit in diode D2 (Figure 8).
Replace the diode is necessary.

Figure 8.D2 and the test points


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 If the voltage value is 0V, check Fuse F1, and the proper connection of the system's
harnesses as follows:
o Power board to Display board (Figure 9 &10)
o Display board to PLC, in and out connections (Figure 11)

Figure 9&10 . Power board to display harness

Figure 11. PLC harnesses

5. Indication test procedure


5.1. Verify ~3V between i1 to i15 on the PLC in Harness (Figure 11)
 If there is no ~3V, try i2 to i15 on the PLC in Harness (Figure 11)
5.2. Now, press the trigger, when the system is turned on, but the program is not set yet,
old the trigger pressed, and verify 24V between i1 /or i2 to i15 (Figure 11)
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Figure 11. Test point on the PLC


5.3. If the measurements are O.K , set the program to light skin , light hair
Then press O.K and realist an IPL pulse:
5.4. Verify that during the pulse creation
5.4.1. The system counts the pulse (Figure12)
5.4.2. The treatment intensity indications LED are flickering (Figure 13)
5.4.2.1. If the system not count the pulse, please returns to Step 4 you miss something.
5.4.2.2. If the LEDs aren't flickering, replace the IPL power board.
5.4.2.3. If it is all O.K, replace the HP, the lamp is broken.

Figure 12. Treatment counter

Figure 13. Treatment intensity indications LED.

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