ATREX BODY SCULPTURE THS01 Specification sheet

BODY SCULPTURE
USE &MAINTENANCE
MANUAL
EN

THS 01
2
SUMMARY
SUMMARY 2
INTRODUCTION 3
WARRANTY CONDITIONS 3
GENERAL INFORMATION AND WARNINGS 4
CONTRAINDICATIONS AND PRECAUTIONS 5
EQUIPMENT AND ACCESSORIES DESCRIPTION 6
METHOD OF USE 7
MAINTENANCE 10
EXTRAORDINARY MAINTENANCE AND FAILURES 11
TECHNICAL SPECIFICATIONS 13
DECLARATION OF CONFORMITY 13
PREMISE
Dear Customer,
Thank you for giving us your trust by choosing a HITECH CRYOTHERM technology.
Your technology has been designed and built to fully meet your current needs, together with
the benefit of your customers.
Before using it, we invite you to read this manual carefully and to keep it carefully: it will allow
you to discover and exploit the full potential of your technologies and keep performance,
safety and reliability levels unaltered over time.
However, you know that you can count on any eventuality on the professional HITECH
CRYOTHERM on the competence of the after-sales service, as well as on our seriousness of
builders.
We wish you good luck.

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WARRANTY CONDITIONS
The equipment is covered by a commercial warranty of 24 months, starting from the delivery
date (the date of the bullet will be used), from construction defects and malfunctions, or in
the case of very intense use, within the first 600 hours of operation.
This guarantee consists in the replacement of any faulty or non-compliant parts from
manufacturing and accidental failures due to the same reasons.
The labor for the replacement of these parts and any transport costs are charged
buyer; any warranty work must always be carried out by qualified personnel of the
manufacturer, or possibly by an approved and authorized center.
The guarantee will not be applied in any case in the following cases:
all breakages or damage caused by negligence, poor routine maintenance, incorrect use of
the equipment, violation of the prescribed instructions, common wear and tear.
HITECH CRYOTHERM
GENERAL INFORMATION AND WARNINGS
EQUIPMENT INTENDED EXCLUSIVELY FOR AESTHETIC USE.
THE EQUIPMENT IS NOT INTENDED FOR USE BY CHILDREN, PEOPLE FROM REDUCED PHYSICAL,
PSYCHIC OR SENSORY CAPACITIES, PERSONNEL WHO HAS NOT BEEN ADEQUATELY
FORMATED AND INSTRUCTED REGARDING THE USE OF THE SAME AND THE RULES THAT
REGULATE THE SAFETY.
All the warnings are available in the manual which can be downloaded from the website
www.cooltherm.co
The appliance has been designed, constructed and protected to be used in a closed
environment, compliant with the provisions of this manual regarding connection to the
network system and environmental data.
The appliance may be used by children aged 8 or less and by persons with reduced physical,
sensory or mental abilities, or lacking experience or necessary knowledge, provided they are
under surveillance or after they have received instructions concerning safe use of the
appliance and an understanding of the dangers inherent to it. Children must not play with the
appliance. Cleaning and maintenance intended for use by the user must not be carried out
by children without supervision.The appliance has a heated surface. Persons insensitive to
heat must be careful when using the appliance. If the power cord is damaged, it must be
replaced by a cable or bya special assembly, available from the manufacturer or his
technical assistance service.
Before putting the equipment into service, make sure that the electrical system of the
structure is equipped with earthing safety devices and an appropriate differential switch in
accordance with current legislation.

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It is forbidden to remove or tamper with safety devices or to modify them.
Do not cover the ventilation openings with drapes, and make sure that they are not blocked
in any way during operation.
Keep the equipment away from splashes of water (equipment not protected against splashes
of water).
Disconnect the power supply from the device when it is not used and / or for all maintenance
and cleaning operations.
In order to eliminate any malfunction, it is necessary to carry out regular checks and to
maintain an adequate cleaning of the equipment and of all the parts that compose it.
Provide for the immediate replacement of worn parts and in any case such as to jeopardize
the safety and proper functioning of the equipment.
The parts of the packaging must not be left within reach of children as they are potential
sources of danger and must, if not stored for transport, be disposed of in compliance with
current legislation.
USAGE PRECAUTIONS
In the preparation and in the course of the treatment, and during the use of the apparatus in
general, it is necessary to avoid some operations, as some precautions are necessary such as:
avoid that the products used should come into contact with the eyes, in the case rinse
thoroughly with water;
do not perform the treatment on the ocular cable;
avoid treatment on areas subject to 24 hours prior to needle or wax depilation treatments of
any kind, or to exfoliating or strong and / or aggressive peeling, both mechanical and
chemical;
absolutely avoid choking electrical connection cables or making creases that prevent
proper connection. Also avoid letting the cables and components be walked on or pinched
even when the equipment is switched off.
carefully clean the surface of the handpieces immediately after finishing the treatment: for
cleaning can be used products based on alcohol or non-aggressive detergents.

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CONTRAINDICATIONS AND PRECAUTIONS
The equipment should only be used in cases and conditions where use is appropriate and
proven to be effective.
Use in the following cases is forbidden:
For cold combined with Ultrasound
- presence of Pace Maker
- angina
- nervous diseases
- asthma
- hemophiliacs
- eczema
- psoriasis
- neuritis
- menstruation (most easily to pain and bleeding)
- pregnancy
- venous and circulation problems
- cardio vascular dysfunction
- feeding time
- fibrocystic mastopathy
- nodules
- presence of intrathsutal metal bodies (prostheses, plates, screws, etc.)
- coagulopathies
- do not treat the abdomen during digestion
The effects of stimulation are effective only in the contact area, therefore, without prejudice
to the general contraindications (eg epilepsy), the others must be interpreted as the
impossibility of carrying out the treatment not to persons burdened by the problems indicated
above, but to the impossibility of carry out the application in the areas burdened by the same
problems.
EQUIPMENT AND ACCESSORIES DESCRIPTION
The equipment consists of the following accessories:
- power supply unit with connection cable to the mains and display block connection cable
- display block with side power button indicated by the 0 / I symbol
- connection cable from display block to band applicator
- connection cable between the two applicators
- two skin applicators
- ergonomic silicone band

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METHOD OF USE
When the device is switched on, the initial screen is displayed and it is possible to continue by
pressing the various buttons.
Figure 1. Mechanical keyboard and display
Button
Functionality
1
AUTOMATIC/MANUAL
2
START
3
UP
4
DOWN
5
STOP
6
BACK/RETURN
1. CONTROLS
1. After one second from power on the display will light up. (see Figure 1.)
START and STOP
2. In normal rest conditions, press START for 1 second, the screen will flash "WORKING"
indicating the cards in operating conditions. (See Figure 2)
3. Under normal operating conditions, press STOP for 1 second, the screen will stop flashing
"WORKING" indicating that the cards will return to sleep mode.
Figure 2. Working condition
OPTIONS

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4. Under normal rest conditions, there are 3 operating options to choose from, classified as
CELLULITE, FAT and MIX. (Refer to Figure 2.)
5. The user is able to exchange the option by pressing UP and DOWN (UP and DOWN).
TC / CYC
6. TC stands for Total Cycle which indicates the total number of cycles that the user intends to
use.
7. CYC stands for Cycle indicating the current time (minutes) left for that particular cycle.
8. The idea of using TC and CYC is to facilitate the user when setting the time interval.
9. User able to press RETURN to set the TC and adjust the value using UP and DOWN (UP AND
DOWN)
AUTOMATIC / MANUAL
10. In normal rest conditions, there are 2 different operating modes, classified as AUTOMATIC
MODE and MANUAL MODE.
11. In AUTOMATIC MODE you have the following preset programs CELLULITE, FAT (adipe) and
MIX (mixed). The programs only work with the default time settings, where the difference in
heat and cold treatment time is set by default.
12. MANUAL MODE is where the CELLULITE, FAT (adipe) and MIX (mixed) options work with the
settings set by the user, where the heat and cold therapy time difference is set according to
the desired MAINTAINER.
13. The user can switch between automatic mode and manual mode by pressing AUTOMATIC
/ MANUAL. (Refer to Figure 3.)

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Figure 3. Manual and automatic screens
WARNING: AN EXCESSIVE INCREASE IN COLD WEATHER AND WARM DURATION MAY CAUSE
A BURNS OF PARTS SUBJECT TO TREATMENT

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EXTRAORDINARY MAINTENANCE AND FAILURES
Repairs must be performed by qualified technical personnel only, as indicated in point 2 of
this manual.
In the event of impacts, tractions, forces, pressures or anything else that could break or alter or
render unusable or not fully functional one or more accessories of the appliance, it will be
possible to replace the pieces requesting them from the trusted seller, identifying the pieces in
question using description or any item number. Spare parts will be supplied at the price list in
force at the time of order, burdened with transport costs and VAT.
If a fault occurs that alters the functionality of the appliance or partially or totally prevents
activation, the appliance must be sent to the manufacturer's premises as provided for in this
manual. HITECH CRYOTHERM declines all responsibility for damage to property or persons
resulting from the use of a device that has shown anomalies or failures of any kind, not sent to
the manufacturer to be reinstated in all its functions, first of all the protections adopted in a
situation of normal functionality of the appliance.
The following table shows a series of cases of malfunctions or generic faults that can help to
diagnose and immediately resolve any minor reversible problems.
INCONVENIENTE
CHECK
The equipment does not turn on
Check the correct connection of the power
cord to the mains socket, and make sure that
the outlet is working
The appliance responds regularly to all
controls, but at the time of start the
applicator does not cools or does not heat.
Possible breakage of the electrical part of
the handpiece connecting cable.
Possible breaking of the electrical part of the
handpiece connection cable.
Contact support
Internal hardware problem, contact support
The monitor turns on, but no command is
issued by the operator
General Hardware Issues ,contact support
STRUCTURAL PARAMETERS
Dimensions: 710 X 300 X 60 mm / Weight: 1KG / ABS / SILICONE / ALUMINUM

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TECHNICAL FEATURES
MODEL : BODY SCULPTURE - THS01
Plate data
Manufacture:
ATREX S.r.l. - ITALY
Model:
THS01
Power Supply:
11V to13,5 Vcc max –81Wmax
Enviromental Data
Temperature Limits:
-10°C / +35°C
Recommended Temp :
0°C / +25°C
Umidity:
fino al 50% a 40°C
Altitude:
2.000 m s.l.m.
DECLARATION OF CONFORMITY
The BODY SCULPTURE - THS01 equipment is designed and built in compliance with the laws in
force in terms of safety and electromagnetic compatibility.
These conformity are certified by specific tests carried out in recognized and accredited
measurement laboratories. The detailed technical files of the final reports are kept and can be
viewed at the manufacturer's premises.
DEGREES OF PROTECTION OF THE APPLIANCE
The appliance is designed and constructed in such a way as to guarantee the following
degrees of protection:
degree of protection against electrical risks of the external casing of the appliance
according to the CEI EN 60529 (CEI 70-1) - IEC 529 standards equal to IP 20;
degree of protection against electrical risks in the control panel of the appliance according
to CEI EN 60529 (CEI 70-1) - IEC 529 standards, equal to IP 42;
degree of pollution of the appliance according to the IEC 947-1 and EN 60947-1 standards
of grade 1.

DICHIARAZIONE DI CONFORMITÀ
DECLARATION OF CONFORMITY
______________________________________________________________________________________
LA SOCIETÀ
The company
ATREX s.r.l. –Via G. Paolo II n°10, 27029 Vigevano (PV) ITALY
Dichiara, sulla base dei test di prova effettuati in laboratorio, che l’apparecchiatura per uso
estetico
Declares, under its own responsability, that the product for aesthetic use
Modello dell’apparecchiatura: THS 01 Marca: ATREX
Device model : THS 01 Brand ATREX
Descrizione dell’apparecchiatura: apparecchio per trattamento di calore parziale
Device description apparatus for partial heat treatment
E’ prodotta in conformità alle seguenti normative:
Is according with the following standard
CEI EN 60601-1 Apparecchi elettromedicali, prescrizioni generali relative alla sicurezza
fondamentale/ CEI EN 60601-1 Medical electrical equipment, general requirements concerning
basic safety
CEI 62-5 III edizione - Apparecchi elettrici per uso estetico/ Electrical appliances for aesthetic use
2006/95/CE Direttiva bassa tensione/Low voltage directive
2004/108/CE Direttiva compatibilità elettromagnetica/ Electromagnetic compatibility directive
EN 61000-3-2 Normativa EMC/EMC Regulation
EBN 61000-3-3 Normativa EMC/EMC Regulation
Decreto n.206 del 28 dicembre 2015 scheda n°13A, identificazione degli apparecchi per uso
estetico/ Decree No. 206 of December 28, 2015 sheet No. 13A, identification of equipment for
aesthetic use
E in accordo con le suddette direttive è stato contrassegnato con marchio
And in accordance with the above directives has been marked
Vigevano, ../../….. ATREX S.r.l.
Il legale rappresentante
Dott.Eugenio Pattacini