Swann CURING LIGHT User manual

Instruction Manual
Please read this manual before operating
RF-SWA-M001-1.1 20210506

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Safety Precautions
1. This product is intended for use in hospitals and dental clinics only. The use of the product must
comply with the requirements of the relevant operating specications and relevant regulations of the
medical department. Users must be professionally trained and qualied as dentists or technicians.
Do not look directly into the light output. Patient, clinician and assistants are always suggested
wearing protectors (safety goggle, face shield…) to avoid crossing infection.
2. The products are reusable:
Prior to each use, place a new barrier sleeve over the curing light Swan. The hygienic barrier sleeve
is customs tted to the curing light and keeps the surface of the curing light clean. The barrier sleeve
helps prevent cross contamination, helps keep dental composite material from adhering to the
surface of the lens and curing light, and prevent discoloration and corrosion from cleaning solutions.
The curing lights must be cleaned and sanitized with appropriate cleaning and/or sanitizing agents
after each patient. The sleeve is not equipped with the curing light. Please note that the sleeve must
meet the requirements of relevant medical device regulation and it’s disposable.
3. During the operation, the light should be aimed straightly at the composite resin to ensure the
eect of solidication.
4. Please use the original light hood and follow the right installation ways to avoid the damage of
blue light to the eyes.
5. Please do not use other than the specied voltage to recharge the battery. Only the original
pedestal charger, adapter and Lithium battery could be used, because other brand pedestal charger,
adapter and Lithium battery are likely to damage the circuit.
6. Please recharge the battery at least 4 hours before rst time usage. It’s forbidden to connect the
charger to the base for long time while not charging and it’s not allowed to use the curing light while
charging.
7. It is forbidden to touch the charging connector with metal or other conductor, to avoiding damage
the circuit of charge or the battery.
8. Please recharge the battery in cool and ventilated room. Please press the main unit to the buckle
of charging base, in order to avoid the poor connection.
9. It is forbidden to self-taking-apart the battery, in order not to result in short-circuit or leakage.
10. It is forbidden to extrude, shake or rock the battery. The Lithium battery is forbidden to be in
short-circuiting situation and it is forbidden to put the battery with metal or other conductors.
11. The instrument has electromagnetic interference. Do not use it around electronic surgery, and
use the instrument with caution in an environment with strong electromagnetic interference.
12. This product does not contain toxic or hazardous substances and it is discarded in accordance
with the relevant laws and regulations on waste medical devices. Please deal with the replaced
battery according to national regulations
13. As a professional manufacturer of medical instruments, we are only responsible for the safety
on the following conditions:
• The maintenance, repair and modication are made by the manufacturer or the authorized dealer.
• The changed components are original of our company and operated correctly according to
instruction manual.
Product contraindications:
The heart disease patient, pregnant woman, children and the person who are allergic to blue light
should be cautious to use this equipment.
Symbol instruction
Symbol Instruction Symbol Instruction
Warning, Caution and Important!
Check the Instruction Manual
Consult the accompanying
documents
Date of manufacture Manufacturer
According to the type of protection
against electric shock: CLASS II
EQUIPMENT
According to the degree of
protection against electric
shock:Type B applied part
Screw inside/ outside Used indoor only
Recovery Keep dry
Handle with care Atmospheric pressure for storage
Temperature limitation for storage Humidity limitation for storage
Appliance compliance WEEE directive,
Dispose as required by the law. CE Mark

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Turn on/o MMode
Authorised Representative in the
EUROPEAN COMMUNITY TTime setting
1 Product introduction
The curing light manufactured by Guilin Rene Medical Instrument Co., Ltd. uses the principle of light radiation
to irradiate photosensitive resin in order to quickly cure it. This product is intended for use in hospitals and dental
clinics and it’s used for prevention and treatment of dental complications of adults or children.
Scope of application: suitable for dentistry, used to cure light-curing materials.
Product composition: main unit, LED light, light hood, charging base, battery and power adapter, etc.
The features of this product are:
1.1 A variety of dierent working modes and working hours can be set.
1.2 Constant light power output, the decrease of battery power will not aect the curing eect.
1. 3 Large-capacity battery. While full charged, under 10 seconds of light per time, it can be used continuously for
more than 500 times.
1. 4 Product schematic
on/off
Screen
Time/mode
Light meter
Power connector
Light guide
light hood
Screen of base
2 Replacement instructions for accessories
Accessories Period of replacement Method of replacement
Power adapter Damaged Replace directly according to the requirements of the manual.
Charging base Damaged Replace directly according to the requirements of the manual.
Battery Damaged Take out the damaged battery and replace it with a new one.
Light hood Damaged Replace directly according to the requirements of the manual.
3 Technical parameters
3.1 Technical Parameters of each model (table 1)
Dimensions Φ86mm*223mm
Net weight 265g
Classied by power supply Powered by rechargeable lithium battery
Input Charging: DC5V 1A Working: 3.6V lithium battery(ICR 18650)
Rechargeable lithium battery
Battery model: ICR 18650
Battery voltage and capacity: 3.6V/2600mAh
The battery has overvoltage, overcurrent and short circuit protection.
Power supply (Adapter) Input : 100-240V AC 50Hz/60Hz 0.4A Max Output: DC 5V/1A
Built-in fuse: T1A 250V
Performance of led lamp
a) 10W high power blue and purple LED lamp.
b) Wave length: 385nm-515nm
c) Category: class I.d)Shoot limit(AEL): 3.9*10―³J
Light Intensity 1000mW/cm²-2500mW/cm²
Inspection method of LED
lamp
When operating correctly, the LED lamp lights up, indicating that the lamp is in
good condition. Dental resin materials commonly used in clinic can match the
wavelength of this curing light, such as 3M, Dentsply and other resins.

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Modes and time setting
TURBO mode: Blue and purple light, 2500mW/cm2 for 1s, 3s
NORMAL mode: Blue and purple light, 1200mW/cm2 for 5s, 10s, 15s, 20s
ORTHO mode: Blue and purple light, 2500mW/cm2 for 3s to work 10 times
every cycle, or 5s to work 10 times every cycle, interval 1s
CHECK mode: purple light, 900mW/cm2 for 30s, 60s
Eective area of irradiation
light 66.4mm²
3.2 Environmental factors
3.2.1 Operation: +5°C - +40°C
3.2.2 Relative humidity: 10% - 93%
3.2.3 Atmospheric pressure: 70kPa-106kPa
3.3 Equipment safety classication
3.3.1 Classied by type of protection against electric shock: Class Ⅱ
3.3.2 Classied by degree of protection against electric shock:Type B application part
3.3.3 Classied according to the degree of protection against incoming liquid: Ordinary equipment (IPXO), non-
waterproof
3.3.4 Classied by operation mode: Short-term operation equipment
3.3.5 Classication of safety degree when using ammable anesthetic gas mixed with air or oxygen or nitrous
oxide: Equipment that cannot be used with ammable anesthetic gas mixed with air or oxygen or nitrous oxide.
4 Installation and demounting
Insert the large end of the light guide (front connector) into the mounting hole at the upper end of the curing light
(please insert it into the bottom in a rotating way, do not be obliquely).
Clamp and install the light hood at the root of the light guide (front joint).
When removing or replacing the light guide, proceed in the opposite direction above.
5 Operation
5.1 When the machine is under stand-by mode, press the time/mode key to light up the screen.
5.2 Mode setting: press the time/mode key for more than 2 seconds to select the mode; during mode switching,
the display screen has a transition picture (the picture shows the full English name of the mode to be switched to),
and every time the key is pressed, there’s a beep. Without operating within 1 minute, the screen will turn o and
the main unit enters the sleep state.
5.3 Time setting: press the time/mode key to select time, see table 1 for settable curing time.
5.4 Point the light guide rod (front connector) light source at the right position, press the switch button and there’s
a beep. The curing light will start to work as the mode setting. The display screen starts counting down from the
selected time, and after the timing ends, the display screen displays the setting time.
5.5 Before the end of setting time, at any time pressing the on/o key can nish the work.
5.6 After the end of an irradiation cycle, you can immediately press the switch to start the next irradiation cycle. If
the handle starts to become hot, please stop working until the handle is completely cooled down. It is recommend-
ed that the number of consecutive irradiations should not exceed 10 times.
5.7 If the transparent cover is stained with resin after use, please wipe it with a cotton cloth to avoid aecting the
light intensity.
5.8 The eective light intensity of this machine is many times higher than that of the halogen lamp curing light, and
the curing depth of the light-curing composite resin is not less than 4mm for 10 seconds.
5.9 The front connector at the front end can be removed, but high temperature and high-pressure sterilization is
not allowed, otherwise it will cause damage.
6 Low battery prompt and charging
6.1 Low voltage indication: The battery symbol on the display starts to icker, accompanied by a sound prompt;
6.2 When charging, insert the charging cable into the TYPE-C socket at the back of the base, the blue light at the
bottom of the base will light up, and the brightness will be changing;
6.3 Correctly put the main unit into the charging base, the base display will automatically light up and display the
power;
6.4 The charging base has a light meter function. When the base is in standby mode, the display is o. Only when
the main unit is charged or when testing light intensity that the display will automatically light up.If it is not charged
or measured, the base display will automatically turn o.
7 Transportation, storage and maintenance
7.1 Transportation
7.1.1 During transportation, avoid shocking and vibration, handle with care and avoid inversion.

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7.1.2 Do not mix with dangerous goods during transportation.
7.1.3 Avoid sunlight, rain or snow during transportation
7.2 Storage
7.2.1 Do not mix with toxic, corrosive, ammable and explosive materials during storage.
7.2.2 The product should be stored in an environment where the relative humidity does not exceed 10% - 93%,
the atmospheric pressure is 70kPa - 106kPa, and the temperature is -20°C - +40°C.
7.3 Maintenance
7.3.1 This equipment should be handled with care, far away from the source of the earthquake, and should be
installed or stored in a cool, dry and ventilated place.
7.3.2 When the device is not in use, turn o the power switch and unplug the power plug; when not in use for a
long time, charge the main unit every 3 months.
7.3.3 To clean or disinfect, wipe the surface with clean water or disinfectant, do not soak.
7.3.4 After use, check if there is any resin remaining on the surface of lamp, so as not to aect the life of the
front joint or aect the curing eect.
8. Troubleshooting
Faulty Possible cause solutions
No reaction
1.Out of battery
2.Faulty of battery
3.Battery protection
1.Charge/Change a new battery
2.Change a new battery
3.Activate it by putting it on the
base
Insucient Light intensity
There is resin remaining on the
surface of the transparent cover
of light guide.
1.Remove the resin
2.Change the transparent cover
Not charging when con-
necting with the adapter
1.The adapter is not connected
well
2.Faulty of adapter or incompat-
ible
3.The charging point is impurity.
1.Reconnect.
2.Change the adapter
3.Clean the inner connector of
charging base by the alcohol
Less working life after
fully charge Capacity of battery decreased Change a new battery
The mode indicator twin-
kles when charging Low voltage Back to normal after 15-minute
charging.
If the fault still cannot be resolved, please contact your local dealer or our company.
9. Electromagnetic compatibility
Attention:
●This Curing Light meets the relevant requirements of YY 0505 standard electromagnetic compatibility. The basic
performance of the light curing machine is: the front LED light can emit blue (UV) when working.
●The user should install and use it according to the electromagnetic compatibility information provided by the
accompanying documents.
●Portable and mobile radio frequency communication equipment may aect the performance of the curing light,
avoid strong electromagnetic interference when using it, such as close to mobile phones, microwave ovens, etc.;
●The guidelines and manufacturer’s declaration are detailed in the attachment.
●Without the express consent of Guilin Rene Medical Instrument Co., Ltd., unauthorized changes or
modications to the equipment may cause damage to the equipment or other
The electromagnetic compatibility of the equipment.
Alert:
●This light curing machine should not be used close to or stacked with other equipment. If it must be used close
or stacked, it should be observed and veried that it can be used in the conguration used.
Normal operation.
● Except for the cables sold by the manufacturer of the curing light as spare parts of internal components, the use
of accessories and cables other than those specied may cause the curing light
Increase in emission or decrease in immunity.
● The following cables must be used to comply with electromagnetic emission and anti-interference requirements:
Cable Name Cable Type Cable Length
Power Line (Output end) Unshielded Parallel Lines 1.2 m
● Key components of electromagnetic compatibility

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The key components of electromagnetic compatibility of this product are IC chip, main PCB, lithium battery, power
adapter and LED lamp. Use or replace the accessories and cables that are not designed to match, will cause
the electromagnetic compatibility emission and anti-interference performance to be signicantly reduced. Do not
change machine parts without authorization.
Enclosure:
Guidance and manufacturer’s declaration - electromagnetic emissions
The models Curing Light are intended for use in the electromagnetic environment specied below. The
customer or the user of the models Curing Light should assure that it is used in such an environment.
Emissions test Compliance Electromagnetic environment - guidance
RF emissionsGB
4824 Group 1
The models Curing Light use RF energy only for its internal function.
Therefore, its RF emissions are very low and are not likely to cause
any interference in nearby electronic equipment.
RF emissionsGB
4824 Class B
The models Curing Light are suitable for used in domestic establish-
ment and in establishment directly connected to a low voltage power
supply network which supplies buildings used for domestic purpos-
es.
Harmonic
emissions
17625.1
Unapplicable
Voltage uctu-
ations / icker
emissions 17625.1
Complies
Guidance & Declaration — electromagnetic immunity
The models Curing Light are intended for use in the electromagnetic environment specied below. The customer
or the user of the models Curing Light should assure that It is used in such an environment.
Immunity test IEC 60601 test level Compliance level Electromagnetic environment - guidance
Electrostatic discharge
(ESD)
GB/T 17626.2
±8 kV contact
±15 kV air
±8 kV contact
±15 kV air
Floors should be wood, concrete or ceramic
tile. If oors are covered with synthetic
material, the relative humidity should be at
least 30 %.
Electrical fast transient/
burst
GB/T 17626.4
±2kV for power supply
lines
±1 kV for Input/output
lines
±2kV for power
supply lines
Mains power quality should be that of a typical
commercial or hospital environment.
Surge
GB/T 17626.5
±1 kV line to line
±2 kV line to earth ±1 kV line to line Mains power quality should be that of a typical
commercial or hospital environment.
Voltage dips, short
interruptions and
voltage variations on
power supply input
lines
GB/T 17626.11
<5 % UT
(>95% dip in UT.) for
0.5 cycle
40 % UT
(60% dip in UT) for 5
cycles
70% UT
(30% dip in UT) for 25
cycles
<5% UT
(>95 % dip in UT) for
5 sec
<5 % UT
(>95% dip in UT.)
for 0.5 cycle
40 % UT
(60% dip in UT)
for 5 cycles
70% UT
(30% dip in UT)
for 25 cycles
<5% UT
(>95 % dip in UT)
for 5 sec
Mains power quality should be that of a typical
commercial or hospital environment. If the user
of the models Curing Light requires continued
operation during power mains interruptions, it
is recommended that the models Curing Light
be powered from an uninterruptible power
supply or a battery.
Power frequency
(50/60 Hz) magnetic
eld
GB/T 17626.8
3A/m 3A/m
Power frequency magnetic elds should be at
levels characteristic of a typical location in a
typical commercial or hospital environment.
NOTE: UT is the a.c. mains voltage prior to application of the test level.
Guidance & Declaration - Electromagnetic immunity
The models Curing Light are intended for use in the electromagnetic environment specied below. The customer
or the user of the models Curing Light should assure that it is used in such an environment.
Immunity test IEC 60601 test
level
Compliance
level Electromagnetic environment - guidance

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Conducted RF
GB/T
17626.6
Radiated RF
GB/T
17626.3
3 Vrms
150 kHz to 80
MHz
3 V/m
80 MHz to 2.5
GHz
3 Vrms
3 V/m
Portable and mobile RF communications equipment should
be used no closer to any part of the models Curing Light,
including cables, than the recommended separation distance
calculated from the equation applicable to the frequency of the
transmitter.
Recommended separation distance
d=[3,5/V1]×P1/2
d=[1.2/E1]×P1/2 80 MHz to 800 MHz
d=[2.3/E1]×P1/2 800 MHz to 2.5 GHz
Where P is the maximum output power rating of the transmitter
in watts (W) according to the transmitter manufacturer and d Is
the recommended separation distance in meters (m).
Field strengths from xed RF transmitters, as determined by
an electromagnetic site survey, a should be less than the com-
pliance level in each frequency range
Interference may occur In the vicinity of equipment marked
with the following symbol:
NOTE: 1 At 80 MHz end 800 MHz the higher frequency range applies.
NOTE: 2 These guidelines may not apply in all situations. Electromagnetic propagation is aected by absorption
and reection from structures, objects and people.
a Field strengths from xed transmitters, such as base stations for radio (cellular/cordless) telephones and land
mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically
with accuracy. To assess the electromagnetic environment due to xed RF transmitters, an electromagnetic site
survey should be considered. If the measured eld strength in the location in which the models Curing Light are
used exceeds the applicable RF compliance level above, the model Curing Light should be observed to verify
normal operation. If abnormal performance is observed, additional measures may be necessary, such as reori-
enting or relocating the models Curing Light.
b Over the frequency range 150 kHz to 80 MHz, eld strengths should be less than 3V/m.
The Rated maximum
output power of
the transmitter
W
The distance between dierent frequencies of the transmitter
150kHz to 80MHz
d=1.2×P1/2
80MHz to 800MHz
d=1.2×P1/2
800MHz to 2,5GHz
d=2.3×P1/2
0.01 0.12 0.12 0.23
0.1 0.38 0.38 0.73
1 1.2 1.22.3 2.3
10 3.8 3.8 7.3
100 12 12 23
For the maximum rated output power of the transmitter not listed in the above table, the recommended separa-
tion distance (d) which in meters (m) that can be determined by the formula in the frequency column of the cor-
responding transmitter. The P is the maximum rated output power of the transmitter provided by the transmitter
manufacturer which in watts (W).
Note 1: At 80MHz and 800MHz frequency points, the higher frequency band formula is used.
Note 2: These guidelines may not be suitable for all situations. Electromagnetic propagation is aected by the
absorption and reection of buildings, objects and human bodies.
10. Environmental protection
Components hazardous substance or element
(Pb) (Hg) (Cd) (Cr6+) (PBB) (PBDE)
Main units ○ ○ ○ ○ ○ ○
Charging base ○ ○ ○ ○ ○ ○
Adaptor ○ ○ ○ ○ ○ ○
Mechanical element (Including screws, nuts, joint rings, etc.) ○ ○ ○ ○ ○ ○
○: Indicates that the content of this toxic and hazardous substance in all homogeneous materials of this
component is below the limit requirement in SJ/T-11363-2006 “Limit Requirements for Toxic and Hazardous
Substances in Electronic Information Products”.
×: It means that the content of this toxic and hazardous substance in at least one of the homogeneous
materials of the part exceeds the limit requirement of SJ/T11363-2006. (This product complies with EU RoHS
environmental protection requirements; currently there is no mature technology in the world that can replace or
reduce the lead content in electronic ceramics, optical glass, steel and copper alloys)
According to the “Administrative Measures for Restricting the Use of Hazardous Substances in Electrical and
Electronic Products”, “Regulations for Recycling and Disposal of Waste Electrical and Electronic Products” and
relevant standards, please comply with the safety and use precautions of the products, and recycle or dispose of
the products in appropriate ways according to local laws and regulations after the use of the products.

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11. After sales service
11.1 If this equipment cannot work normally due to quality problems from the date of sale, please show the
warranty card and our company will be responsible for the maintenance. Please refer to the product warranty card
for the warranty period and warranty scope.
11.2 This product does not contain replaceable parts. All maintenance, adjustment, calibration and modication of
technical parameters of the product can only be carried out by our company’s technicians or special repair shops.
If customers need to repair themselves, our company can provide them on request Circuit diagrams, component
lists, legends, calibration specications, or other materials needed to help qualied technical personnel repair the
equipment parts designated by our company, but we will not bear any consequences.
11.3 The user must use the original parts, purchase please contact with the local dealer or the manufaturer. Do
not use the related accessories of other brands, so as not to cause damage to the light curing machine or other
dangers.
11.4 After the power adapter, charging base and other accessories are damaged, users should not repair by
themselves. Please buy new parts and replace them by yourself. If you need relevant information, please contact
the manufacturer.
12. Special instructions
The company reserves the right to modify the machine design, product technology or accessories, operation
manual and machine packaging content at any time without prior notice. The product is subject to the real object,
and the picture is for reference only. The nal interpretation right belongs to
Guilin Rene Medical Instrument CO., LTD.
After service and Warranty Instruction
1 Period validity: two year’s free repair for the main unit, charging base, power adapter from the date of purchase.
One year’s free repair for lithium battery. Warranty card is necessary while submitting the repairing request.
2 Range of warranty: Within the warranty period of validity, we are responsible for any troubles caused by quality
problems or products technique and structure.
3 The followings are beyond our warranty:
1) The damage caused by disobeying the operation instruction or lack of the needed condition.
2) The damage caused by unsuitable operation or disassembly without authorization.
3) The damage caused by unadvisable transportation or preservation.
4) There isn’t the seal of distributor or the warranty card isn’t lled in completed.
5) Light tip and protective light shield.
After service card
Name of
Customer
Address
Post Code Tel
E-mail
Purchase Date Production Date
Distributor
Model Product No.
Guilin Rene Medical Instrument Co., Ltd.
No.8-3, Information Industrial Park, High-Tech Zone, Qixing District, Guilin, Guangxi, 541004, P.R. China
Tel: +86-773-7796686 Email:rene@rene-med.com Website: http://www.rene-med.com
MedNet EC-REP GmbH
Borkstrasse 10 · 48163 Muenster · Germany
Product life: 5 years
Production date: please refer to packaging label.

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