Tecnomed Italia STERIL FAN SFA2030F User manual

STERIL FAN
Wall-mounted UVGI air sterilizer
SFA2030F // SFA2045F
V.8.00

CONTENTS
SECTION
1- SYMBOLS
1.1- WARNING IDENTIFICATION
2- GENERAL WARNINGS
2.1- GENERAL CHECK
2.2- TRANSPORT DAMAGE IN ITALY FREIGHT PRE-PAID
2.3- TRANSPORT DAMAGE OUTSIDE ITALY FREIGHT PRE-PAID
2.4- TRANSPORT AND STORAGE CONDITIONS
3- INSTALLATION SAFETY RULES
3.1- WORKING ENVIRONMENT
4- SAFETY REQUIREMENTS
4.1- SAFETY REQUIREMENTS
5- PRODUCT DESCRIPTION
5.1- INTENDED USE
5.2- STANDARDS/APPROVALS
5.3- TECHNICAL SPECIFICATIONS
5.4- NAMEPLATES
5.5- PRODUCT PROFILE
5.6- STRUCTURE OF AIR TREATMENT
6- INSTALLATION
6.1- ELECTRICAL PREPARATION
6.2 - WALL MOUNTING
6.3 - RECOMMENDED POSITIONING IN A DENTAL TREATMENT ROOM
7- INSTRUCTIONS FOR USE
7.1 - REMOTE CONTROL OVERVIEW
7.2 - INSERTING REMOTE CONTROL BATTERIES
PAGE
2
3
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4
4
5
5
6
7
8
9
10
10
11
12
13
14
15
15
15
16
18
18
19
19

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7.3 - RESET WEEK
7.4 - SETTING THE TIME
7.5 - LCD DISPLAY
7.6 - MEMORY FUNCTION
7.7 - SETTINGS INSTRUCTIONS
8- CLEANING
8.1- RECOMMENDED DISINFECTANT
9- ROUTINE MAINTENANCE
10- TROUBLESHOOTING
11- EXTRAORDINARY MAINTENANCE
11.1- MAINTENANCE TABLE RESERVED FOR TECHNICAL SUPPORT
11.2- TECHNICAL TROUBLESHOOTING
11.3- REPLACING THE PHOTOCATALYTIC FILTER
11.4- CLEANING OR REPLACING THE UVC LAMP
11.5- REPLACING THE FUSES
12- RELATED ITEMS
13- DISPOSAL
14- WARRANTY
DECLARATION OF CONFORMITY
CERTIFICATE OF WARRANTY
20
20
21
21
22
29
29
30
31
32
33
34
35
36
37
38
38
39
40
41

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1- SYMBOLS
CE MARKING. This product bears the CE mark according to the rules indicated in the
standards EN 60335 - CEI EN 62233 - CEI EN 61000 - CEI EN 55014 and the directives
2014/30/EU - 2014/35/EU.
Protection type against direct and indirect contacts: Class I.
EARTHING SYMBOL. This symbol indicates the presence of a protective earthing
contact.
INSTRUCTIONS FOR OPERATION. This symbol on the product indicates that the user ma-
nual must be consulted before using the equipment.
HAZARD SYMBOL. It indicates a dangerous situation that might result in moderate
or severe/fatal injuries unless avoided.
WARNING SYMBOL. It indicates a hazardous situation that might result in moderate
to minor injury or property damage.
DO NOT TOUCH WITH WET HANDS SYMBOL. This symbol indicates that you should not
touch the device with wet hands.
UVC HAZARD SYMBOL: articial optical radiation (AOR) hazard
GENERAL INFORMATION SYMBOL. This symbol indicates information that allows you
to use the device more effectively.
DISPOSAL SYMBOL. This symbol found on the product indicates that the equipment
cannot be treated as normal household waste in accordance with Directives
2002/95/EC, 2002/96/EC and 2003/108/EC.
FRAGILE SYMBOL. This symbol indicates that the product inside the box is fragile.
Avoid impacts.
PROTECT FROM HUMIDITY SYMBOL. This symbol indicates to keep the box away
from water and moisture.
UP SYMBOL. Transport and store the product only in the direction indicated by the
arrows.
DO NOT STACK SYMBOL.
TEMPERATURE LIMIT SYMBOL. From -10° to 45°C.
HUMIDITY LIMIT SYMBOL. From 10 to 90%.
ATMOSPHERIC PRESSURE LIMIT SYMBOL. From 500 to 1060 hPa.

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1.1- WARNING IDENTIFICATION
It indicates a dangerous situation that might result in moderate or severe/fatal injuries
unless avoided.
It indicates a dangerous situation that might result in moderate or mild injuries or da-
mage to property unless avoided.
This symbol indicates that you should not touch the device with wet hands.
This symbol indicates an articial optical radiation (AOR) hazard. Possible damage
to eyes and skin.
This icon represents useful information.
2 - GENERAL WARNINGS
•Read this manual carefully before carrying out any operation on the product, follow the
warnings contained in it and keep it for future reference.
•This manual is intended to provide the user with instructions for correct installation and
use of the product.
•The product must be used in compliance with the procedures contained in the user ma-
nual and never for purposes other than those specied therein.
•The user is legally responsible for the installation, operation and maintenance of the
equipment itself.
•The manual describes all product versions and optionals, therefore not all instructions are
applicable to your product.
•The information, technical specications, illustrations contained in this publication
•are not binding.
•Tecnomed Italia s.r.l. has adopted a policy of constant product improvement and reser-
ves the right to make changes to this manual or to the product itself without prior notice,
as long as such changes do not affect safe use of the device.
•Keep the manual within reach.
•Furthermore, any kind of reproduction or appropriation of the text and/or images in the
manual is absolutely forbidden, therefore some instructions, specications and images
contained in this manual may differ slightly from the product purchased.
•All the material contained in this manual is owned by Tecnomed Italia and/or by
•companies representing it. The images are not binding and are purely illustrative.
•If the appliance is resold, it must be sent to the new owner with this manual.
•The original text of this manual is in English.
DANGER! Modifying the appliance is strictly forbidden. Tecnomed Italia s.r.l. assumes
NO responsibility for personal injury and/or direct or indirect property damage resulting
from non-compliance with this requirement.
DANGER! Tecnomed Italia s.r.l. assumes no responsibility, express or implied, and cannot
be held liable for injuries to persons and/or direct or indirect damage to property, resulting
from the non-observance of what is reported in the entire manual and/or as a result of incor-
rect procedures related to the installation and/or use of the appliance and its accessories
and/or resulting from poor and/or lack of cleaning and/or maintenance.

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2.1 - GENERAL CHECK
WARNING! Upon delivery of the product, check that there are no signs of impact
andthat the packaging is intact. Otherwise, follow the indications in paragraph 2.2 or 2.3.
2.2 - TRANSPORT DAMAGE IN ITALY FREIGHT PRE-PAID
Upon delivery, if the package/parcel shows visible signs of damage, the recipient must or
may sign the delivery note conditionally, reserving the right to claim for any damages. Ita-
lian law prescribes that “the unconditional acceptance of delivery of the goods transpor-
ted by the consignee, together with the payment of what is due to the carrier, extinguishes
the causes of action arising from the contract, except in case of fraud or gross negligence
of the carrier” (art. 1698 Italian Civil Code). To conditionally accept a parcel it is necessary
to use specic elds in the document (delivery note) that the carrier will ask you to sign
upon delivery. Each carrier has its own procedure for signing
conditionally, you will need to ask them how to proceed.
If the packaging is visibly damaged upon delivery, proceeds follows:
1. Check the appearance and the condition of the packages. Check that it is not da-
maged, intact, and that everything is there: if the document indicates there are several
packages, check that they are all there. The recipient and the employee of the transport
company sign the delivery note adding that a more detailed inspection is required, clearly
stating the reason:
- “goods conditionally accepted subject to detailed inspection”
- “package with packaging tape added, goods conditionally accepted subject to detai-
led inspection”
- “cardboard package with obvious signs of warping/folding, goods conditionally accep-
ted subject to detailed inspection”
- “package externally damaged and/or partially opened, goods conditionally accepted
subject to detailed inspection”
2. Leave the product and the packaging as they are. Document the damaged package/
parcel with photos and/or videos.
3. Do not use the product.
4. Report the damages to the transport company.
5. Report the damage to Tecnomed Italia s.r.l. ([email protected]).
6. In no case must the product be returned to Tecnomed Italia s.r.l. before having received
a reply and authorisation to do so.
7. Send the signed delivery note to Tecnomed Italia srl.
8. Leave the product and the packaging as they are.
9. Do not use the product.
Note: If you are concerned that there may be damage hidden and not visible from
the outside, please conditionally sign anyway.
If the product is damaged, but no damage to the packaging was detected at the time of
delivery, follow these steps:
1. Inform the transport company no later than 7 days after delivery.
2. Report the damage to Tecnomed Italia s.r.l. ([email protected]) by sending visual
proof of the unpacked product.
3. Leave the product as it is
WARNING! If the recipient fails to comply with any of the provisions stated above, the
damage shall be considered to have arisen after delivery.

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2.3 - TRANSPORT DAMAGE OUTSIDE ITALY FREIGHT PRE-PAID
WARNING! Tecnomed Italy srl shall not be liable for damages occurred during transit.
Check the goods immediately upon receipt!
If the packaging is visibly damaged upon delivery, follow these steps:
1. The recipient must acknowledge the loss or damage on the delivery note. The recipient
and the employee of the transport company sign the delivery note. Only on the basis of this
proof can the recipient assert the claim for replacement for damage by the transport com-
pany.
2. Leave the product and the packaging as they are.
3. Do not use the product.
If the product is damaged, but no damage to the packaging was detected at the time of
delivery, follow these steps:
1. Notify the transport company no later than 30 days after delivery.
2. Leave the product and the packaging as they are.
3. Do not use the faulty product.
WARNING! If the recipient fails to comply with any of the aforementioned provisions, the
damage shall be considered as if arising after delivery.
WARNING! If the goods travel carriage forward, the responsibility lies between the buyer
and the carrier. Tecnomed Italia will have no responsibility.
2.4 - TRANSPORT AND STORAGE CONDITIONS
The product inside the packaging is fragile. Avoid shocks.
Keep the package away from water and humidity.
Transport and store the product only in the direction indicated by the arrows.
Do not stack.
Temperature limit: from -10° to 45° C.
Humidity limit: from 10 to 90%.
Atmospheric pressure limit: from 500 to 1060 hPa.

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3- INSTALLATION SAFETY RULES
DANGER! Do not operate the appliance if light shines out of it. IT MAY RESULT IN EYE
AND SKIN DAMAGE.
DANGER! The product is intended for indoor use only, it is not suitable for wet or humid
environments.
DANGER! Do not install the appliance in places where there are anaesthetic or amma-
ble gases, or in places with harmful chemical air.
DANGER! The appliance must not be used in a potentially explosive atmosphere.
DANGER! You must not cover, block or obstruct, even partially, the air inlet and outlet
vents- doing so will compromise the effectiveness of the disinfection.
DANGER! Install the appliance in a place protected from impact or accidental splashes
of water or liquids.
DANGER! Do not install the device near heat sources or in places with high temperatu-
res. Install it in such a way that there is adequate air circulation around it.
DANGER! Before proceeding with installation, check the device condition; if it shows
signs of damage caused during transport, do not start it and contact Tecnomed Italia s.r.l.
as per paragraph 2.1.
DANGER! Faulty components must only be replaced with original spare parts.
DANGER! Modifying the appliance is strictly forbidden. Tecnomed Italia s.r.l. assumes
NO responsibility for personal injury and/or direct or indirect property damage resulting from
non-compliance with this requirement.
DANGER! Respect the operating conditions specied in the “Technical Specications”
paragraph and do not exceed the prescribed values.
WARNING! Before connecting the power cable, make sure that the electrical contacts
are perfectly dry. If necessary, use compressed air to dry them.
DANGER! The electrical system of the premises in which the purchased product is used
must comply with CEI 64-8/7 standards and subsequent amendments. The appliance must
be installed by qualied personnel only.
DANGER! To avoid the risk of electric shock, this appliance must only be connected to
an electrical system with protective earth.
WARNING! Check that the power supply voltage indicated on the label is
the same as the mains voltage.

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WARNING! In order to guarantee the functionality and safety of the product and
avoid damage caused by wear, it is necessary to carry out routine and extraordinary main-
tenance at pre-established intervals, by contacting your local Tecnomed Italia s.r.l. dealer.
For further information, see the paragraph “Maintenance” on page 28.
DANGER! Tecnomed Italia s.r.l. assumes no responsibility, express or implied, and can-
not be held liable for injuries to persons and/or direct or indirect damage to property, resul-
ting from the non-observance of what is reported in the entire manual and/or as a result of
incorrect procedures related to the installation and/or use of the appliance and its acces-
sories and/or resulting from poor and/or lack of cleaning and/or maintenance.
DANGER! Do not disassemble the device. In case of malfunction, please contact an
authorised Tecnomed Italia s.r.l. centre.
WARNING! Tecnomed Italia s.r.l. stipulates that in order to ensure device operational
safety, installation, maintenance and repairs of this product must only be carried out by
technicians authorised by Tecnomed Italia s.r.l.
DANGER! Any technician or worker who is not authorised by Tecnomed Italia s.r.l. and
who proceeds to modify/alter the product by replacing parts or components with others
not used by the manufacturer, assumes the responsibility similar to that of the manufacturer.
TECNOMED ITALIA S.R.L. IS ONLY RESPONSIBLE FOR THE SAFETY AND GUARANTEES
THEPRODUCT IF WHAT IS WRITTEN IN THIS MANUAL IS OBSERVED.
For any request, always indicate the date of purchase, the device model and serial num-
ber. For information on technical support contact:[email protected]
3.1 - WORKING ENVIRONMENT
ENVIRONMENTAL REQUIREMENTS:
• Environmental temperature: from +10°C to + 40°C.
• Optimum environmental temperature: from 15°C to 30°C.
• Relative air humidity: from 30 to 75%.
• Ambient pressure from 600 to 1060 hpa

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4 - SAFETY REQUIREMENTS
DANGER! Do not operate the appliance if light shines out of it. IT MAY RESULT IN EYE
AND SKIN DAMAGE
DANGER! The product is intended for indoor use only, it is not suitable for wet or humid
environments.
DANGER! Do not install the appliance in places where there are anaesthetic or amma-
ble gases, or in places with harmful chemical air.
DANGER! The device must not be used in a potentially explosive atmosphere.
DANGER! You must not cover, block or obstruct, even partially, the
air inlet and outlet vents- doing so will compromise the effectiveness of the disinfection.
DANGER! Use the appliance in a place protected from impact or accidental splashes
of water or liquids.
DANGER! Do not use the device near heat sources or in places with high temperatures.
Use it in such a way that there is adequate air circulation around it.
DANGER! Do not operate the appliance if it shows signs of damage. Contact Tecno-
med Italia s.r.l. as per paragraph 2.1.
DANGER! Use the device only for the intended use that is foreseen for it. Failure to
comply with this may cause serious injury to the patient, the operator and damage to the
device..
DANGER! The electrical system of the premises in which the purchased product is
used must comply with CEI 64-8/7 standards and subsequent amendments. The appliance
must only be installed by technical personnel authorised by Tecnomed Italia s.r.l.
DANGER! Always check the appliance and the accessories are in proper working or-
der. Always check that there is no water underneath the device. Do not use if there are
operating faults. In case of anomalies, contact a service centre authorised by Tecnomed
Italia s.r.l.
DANGER! Modifying the appliance is strictly forbidden. Tecnomed Italia s.r.l. is NOT
responsible for personal injury and/or direct or indirect property damage resulting from
non-compliance with this requirement.
WARNING! In order to guarantee the functionality and safety of the product and to
avoid damage caused by wear, it is necessary to carry out routine and extraordinary main-
tenance (by contacting a centre authorised by Tecnomed Italia s.r.l.), at pre-established
intervals. For further information, see the paragraph “Maintenance” on page 28.

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DANGER! For maintenance and cleaning, disconnect the appliance by unplugging it
from the wall socket.
WARNING! Only use products for care and cleaning authorised by Tecnomed
Italia s.r.l. Unsuitable products can damage the surface of the device, affect its operation,
cause contamination, cause injury to patients and/or the operator. Tecnomed Italia s.r.l.
assumes NO responsibility for personal injury and/or direct or indirect property damage re-
sulting from non-compliance with this requirement. For further information, see the para-
graph “Cleaning” page 27.
DANGER! In the event of a malfunction that is not described in this documentation, put
the product out of service and contact an authorised Tecnomed Italia s.r.l. technician.
DANGER! Do not disassemble the device. In case of malfunction, please contact an
authorised Tecnomed Italia s.r.l. centre.
DANGER! Tecnomed Italia s.r.l. assumes no responsibility, express or implied, and cannot
be held liable for injuries to persons and/or direct or indirect damage to property, resulting
from the non-observance of what is reported in the entire manual and/or as a result of incor-
rect procedures related to the installation and/or use of the appliance and its accessories
and/or resulting from poor and/or lack of cleaning and/or maintenance.
4.1 SAFETY REQUIREMENTS
Tecnomed Italia s.r.l. assumes no responsibility, express or implicit, and cannot be held liable
for injuries to persons and/or direct or indirect damage to property, resulting from the non-
observance of what is reported in the entire manual and/or as a result of incorrect procedures
related to the installation and/or use of the appliance and its accessories and/or resulting
from poor and/or lack of cleaning and/or maintenance. Tecnomed Italia s.r.l. cannot be held
responsible, expressly or implicitly, for any type of injury to persons and/or damage to property,
carried out by the user of the product and its accessories, due to the following:
• If the appliance is used for purposes other than those for which it is intended;
• If the appliance is not used in accordance with all instructions and requirements described
in this manual;
• Lack of spare parts to use in the event of a breakdown due to faults or problems;
• Use of accessories not authorised by Tecnomed Italia s.r.l.;
• If the electrical system where the appliance is installed does not comply with the standard of
appropriate application and requirements;
• If the assembly and/or any repairs have been carried out by personnel
not authorised by Tecnomed Italia s.r.l.;
• If the environmental conditions in which the device is stored do not meet the requirements
indicated in the chapter “Transport and storage conditions”.

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5- PRODUCT DESCRIPTION
5.1 - INTENDED USE
The Steril Fan line includes biological air treatment equipment, ensuring the elimination of
all pathogens such as bacteria, viruses, fungi and moulds present in the air. The internal
UVC lamps and a series of special lters allow the device to guarantee constant room
sanitising. Furthermore, it should be noted that, every time air passes through the germicidal
chamber, it is puried and up to 99.99% of germs are killed.
This appliance is intended for air disinfection only. Any other use is to be considered
improper and therefore dangerous.
The equipment is intended for use in hospital emergency rooms, operating rooms, infusion
rooms, delivery rooms, intensive care units, general wards, health practices, dental
practices, pharmacies, grocery stores, companies and waiting rooms.
DANGER! This appliance is not intended for use in areas exposed to the risk of explosion.
DANGER! The product is intended for indoor use only, it is not suitable for wet or humid
environments.
The user must comply with the following:
1 - Use only EC certied devices in perfect state.
2 - Protect himself, the patients and any third parties from any hazards.
3 - Avoid any contamination of the product.
National regulations in force when using the product, in particular:
1 - Current provisions on occupational safety.
2 - Current measures on accident prevention.
DANGER! Use the device only for the intended use that is foreseen for it. Failure to
comply with this may cause serious injury to the patient, the operator and damage to the
device.
DANGER! Tecnomed Italia s.r.l. assumes no responsibility, express or implied, and can-
not be held liable for injuries to persons and/or direct or indirect damage to property, resul-
ting from the non-observance of what is reported in the entire manual and/or as a result of
incorrect procedures related to the installation and/or use of the appliance and its acces-
sories and/or resulting from poor and/or lack of cleaning and/or maintenance.

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5.2 - STANDARDS/APPROVALS
Medical device
The STERIL FAN device bears the CE mark.
The STERIL FAN device is a device with electrical protection class I.
Equipment safety: The inductor and light wave controller have signal feedback and anti -
interference control.
The STERIL FAN device also complies with the following standards:
Numero Titolo
EN60335-2-65:2003 +
A1:2008 + A11:2012
HOUSEHOLD AND SIMILAR ELECTRICAL APPLIANCES - SA-
FETY - PART 2: SPECIAL REQUIREMENTS FOR AIR CLEANING
APPLIANCES
EN60335-1:2012 +
AC:2014 + A11:2014 +
A13:2017
HOUSEHOLD APPLIANCES AND SIMILAR APPLIANCES - SAFETY
PART 1: GENERAL REQUIREMENTS
EN62233:2008
STANDARDS ON MEASUREMENT METHODS FOR ELECTROMA-
GNETIC FIELDS OF HOUSEHOLD APPLIANCES AND SIMILAR
EQUIPMENT WITH REGARD TO HUMAN EXPOSURE.
EN61000-3-2:2014
EN61000-3-3:2013
EN55014-1:2017
EN55014-2:2015
STANDARDS ON ELECTROMAGNETIC COMPATIBILITY (EMC)
- REQUIREMENTS FOR HOUSEHOLD APPLIANCES, ELECTRICAL
TOOLS AND SIMILAR EQUIPMENT
2014/35/EU LOW VOLTAGE DIRECTIVE
2014/30/EU ELECTROMAGNETIC COMPATIBILITY DIRECTIVE

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5.3 - CARATTERISTICHE TECNICHE
Codice SFA2030F SFA2045F
Flow rate m3/h 800 m3/h 1200 m3/h
Room coverage m230 m 45 m
Room coverage m390 m 135 m
Max. Watt power 95 W 120 W
Primary dust lter YES (code SFA20T.1) YES (code SFA20T.1)
Carbon lter NO NO
TiO2 photocatalytic lter SINGLE (cod. SFA20T.2) SINGLE (cod. SFA20T.2)
UVC lamp 1X20W (code SFA20T.3) 1X20W (code SFA20T.3)
Ultraviolet intensity 20102 um/cm2 20102 um/cm2
UVC wavelength 253.7 nm 253.7 nm
HEPA lter NO NO
Recirculation speed 3 speeds 3 speeds
Max noise db S 55 db S 55 db
Operation manual-programmable manual-programmable
Remote control ALL THREE LEDS DL1 DL2
DL3
ALL THREE LEDS DL1 DL2
DL3
Critical operation alarm YES - 3 alarms YES - 3 alarms
Lamp life 12000 h (approx. 4 years) 12000 h (approx. 4 years)
External emission µvc at 1 cm S 5 µw/cm2S 5 µw/cm2
Microbiological elimination% 99.90% 99.90%
Ozone emission 0,003 mg/m30,003 mg/m3
Weight 11 kg 11 kg
Dimensions 1000x330x200 mm
(wxdxh)
1000x330x200 mm
(wxdxh)
Sterilisation effect (disinfection time with air volume at maximum power 30/90 min)
- Percent of staphylococcus aureus eliminated S99.90%
- Percent of natural bacteria and viruses in the air eliminated S90.0%
The method of physical sterilisation and purication is adopted. During the operation of the
device no gases and harmful substances are generated and the device can be used with
people present.
Fusibili
Identicazione Valore Dimensione Protezione Posizione
FUSE1-2 F2,5
TIME-DELAY 5x20 230VAC Under the right side cover
MANCA FOTO TARGHETTA

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Packing dimensions:
• Code SFA2030F: PACK 1 TECNOMED ITALIA - Box
Dimensions 400X1000X270 mm (width x depth x height). Weight 13 kg (approx).
• Code SFA2045F: PACK 1 TECNOMED ITALIA - Box
Dimensions 400X1000X270 mm (width x depth x height). Weight 13 kg (approx).
5.4 - NAMEPLATES
The nameplate is located on the left side of the device:
Data on the plate
• Importer’s name
• Manufacturer’s name
• Model
• Reference code
• Serial number
• Power
• Voltage
• Consumption
• Air circulation ow
• Protection class
• Regulatory symbols
• Brand

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5.5 - PRODUCT PROFILE
The equipment is composed of a primary lter, a UVC light wave inductor with TiO2
photocatalytic lter, a tangential fan and a radio-controlled electronic control unit. The
structure is as follows:
A B C D
E
F
A
A. Primary lters
B. TiO2 photocatalytic lter
C. UVC germicidal lamp
D. PCB main drive
E. Swing motor
F. Tangential fan
G
I
J
H
K
G. PCB Display
H. Infrared sensor
I. Cover
J. Directional aps
K. Power cable 1.4 mt

15
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5.5 - PRODUCT PROFILE
The equipment is composed of a primary lter, a UVC light wave inductor with TiO2
photocatalytic lter, a tangential fan and a radio-controlled electronic control unit. The
structure is as follows:
ABC D
E
F
A
A. Primary lters
B. TiO2 photocatalytic lter
C. UVC germicidal lamp
D. PCB main drive
E. Swing motor
F. Tangential fan
G
I
J
H
K
G. PCB Display
H. Infrared sensor
I. Cover
J. Directional aps
K. Power cable 1.4 mt
5.6 - STRUCTURE OF AIR TREATMENT
3
Photocatalytic
lter
Sterilises the air
1
Primary lter
Removes dust
and impurities
2
UVC rays light
Puries the air
6- INSTALLATION
DANGER! Carefully read the paragraph “Installation safety regulations” page 4 before
proceeding.
DANGER! Before proceeding with the assembly/mounting operations it is necessary to
make sure that the wall is able to support the device. The expansion plugs supplied must
ONLY be used with the following wall types: concrete, natural stone, concrete or brick. THEY
ARE NOT SUITABLE FOR OTHER TYPES OF MATERIAL.
DANGER! Tecnomed Italia s.r.l. assumes no responsibility, express or implied, and can-
not be held liable for injuries to persons and/or direct or indirect damage to property, resul-
ting from the non-observance of what is reported in the entire manual and/or as a result of
incorrect procedures related to the installation and/or use of the appliance and its acces-
sories and/or resulting from poor and/or lack of cleaning and/or maintenance.
6.1 - ELECTRICAL PREPARATION
To operate the appliance, only a 230/240 Volt - 50 Hz power supply is required.
1. Socket power supply connection.
A schuko socket can be installed near the appliance.

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2. Fixed mains power supply connection
Create a mains supply conduit on the wall with a 3x1.5 mm3 cable at the point
indicated.
Mains power
supply 3 x 1,5
mm
6.2 - WALL MOUNTING
1. Position the wall support bracket level to determine the installation position of the
machine and mark the 3 holes for drilling.
560 mm
2. Drill the wall with a 10 mm wall bit.
3. Fix the bracket on the wall with the 3 sher screws supplied
In case of mounting on plasterboard, use special sher screws and x the bracket
with 5 expansion plugs.
4. Secure the panel to the wall with washers and M8 nuts.

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5. Hook Steril Fan onto the wall bracket.
6. In case of socket power supply connection, make sure that the socket is earthed and
connect the power supply by inserting the schuko plug. In the case of xed mains
power supply connection, cut off the plug and connect the cable using an insulated
terminal block.
7. As soon as it is powered, the time (not synchronised) and the ambient temperature
will appear on the display and a short acoustic signal will be heard.
WARNING! In order to guarantee appliance operation, a minimum distance of 50 cm
from the false ceiling is recommended. The optimal positioning height of the appliance
from the oor varies from 2.3 to 2.5 metres.
min 0,5 mt
min 2,3 mt - max 2,5 mt
6.3 - RECOMMENDED POSITIONING IN A DENTAL TREATMENT ROOM
If possible, install STERIL FAN on the wall at the foot of the chair.

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STERIL FAN
7- INSTRUCTIONS FOR USE
DANGER! Carefully read the paragraph “Installation safety regulations” page
6 before proceeding to use.
WARNING! If used in manual mode, switch off the machine at the end of the day
using the “P” key on the remote control.
WARNING! When the machine is running, doors and windows must be closed.
WARNING! In the event of a malfunction that is not described in this documentation,
put the product out of service and contact an authorised Tecnomed Italia s.r.l. techni-
cian.
DANGER! Before proceeding with use, carefully read all the previous paragraphs, paying
particular attention to the paragraph “Safety requirements” page 8.
DANGER! Tecnomed Italia s.r.l. assumes no responsibility, express or implied, and can-
not be held liable for injuries to persons and/or direct or indirect damage to property, re-
sulting from the non-observance of what is reported in the entire manual and/or as a re-
sult of incorrect procedures related to the installation and/or use of the appliance and its
accessories and/or resulting from poor and/or lack of cleaning and/or maintenance.