marsden UFR118 User manual

-
Version 1.7 10/20
UFR118 (T-210)
Infrared Thermometer
User Manual

2
Contents
Introduction 3
Declaration of Conformity 3
Specification 4
Symbol Descriptions 4
Important Safety Instructions 5
Parts Identification 6
Battery Installation 7
About Normal Temperature & Fever 8
Unit Setting 9
Operation 9
Error Messages 11
Warranty 11
EMC Declaraton 12

3
Thank you for purchasing this Marsden UFR118 Infrared Thermometer. This
thermometer is designed for screening multiple individuals for high temperature, and
can be used with individualsofallages. To ensure accurate use of the UFR118, please
read this user manual before use and keep for future reference.
Declaration of Conformity
●This product is approved under MDD 93/42/EEC Medical Devices Directive.
●Full responsibility for the conformance of this product to the Standard is assumed by
Shenzhen Urion Technology Co., Ltd, Floor 4-6th Floor Building D, Jiale Science &
Technology Industrial Zone, No.3, ChuangWei Road, Heshuikou Community, MaTian
Street, GuangMing New District, 518106 Shenzen.
EN 60601-
1-2:2015
Medical electrical equipment -- Part 1-2: General requirements for basic safety and essential
performance - Collateral standard: Electromagnetic disturbances - Requirements and tests
IEC 60601-
1-2:2014
Medical electrical equipment -- Part 1-2: General requirements for basic safety and essential
performance - Collateral standard: Electromagnetic disturbances - Requirements and tests
EN 60601-
1-11:2015
Medical electrical equipment –Part 1-11: General requirements for basic safety and essential
performance –Collateral Standard: Requirements for medical electrical equipment and medical
electrical systems used in the home healthcare environment Clause 12 of IEC 60601-1-11
IEC 60601-
1-11:2015
Medical electrical equipment –Part 1-11: General requirements for basic safety and essential
performance –Collateral Standard: Requirements for medical electrical equipment and medical
electrical systems used in the home healthcare environment Clause 12 of IEC 60601-1-11
ISO 80601-
2-56:2017
Medical electrical equipment —Part 2-56: Particular requirements for basic safety and essential
performance of clinical thermometers for body temperature measurement Clause 202 of ISO
80601-2-56
This does not guarantee in any way that the device will not be affected by electromagnetic interference. Avoid
using the device in a high electromagnetic environment.
Classification
1.Internally powered equipment;
2. Type BF applied part;
3. Protection against ingress of water or particulate matter: IP21;
4. Not category AP/APG equipment;
5. Mode of operation: Continuous operation.
Note: the user must check that the equipment functions safely and ensure that it is in proper
working condition before it being used.

4
Specification
Measurement Range
32ºC - 43ºC ± 0.2ºC
Accuracy
± 0.2ºC / ± 0.2ºF
Measuring Distance
1cm –10cm
Display
LED
Response Time
1 second
Measuring localisation
Forehead
Installation Method
Nail hook, double sided sticking tape, bracket for stand
LED Colour Indicator
Green: Temperature <37.5ºC (99ºF) Red: Temperature ≥37.5ºC
(99ºF)
Power
18650 lithium battery 2000mAh/Type-C
Unit Weight
Approx. 151g (excluding batteries)
Dimensions
140mm x 93mm x 93mm
Battery Life
Upto 300 temperature measurements
Operating Environment
Body mode 10ºC ~ 40ºC / 50ºF - 104℉
Storage and Shipping
Environment
Ambient temperature range：-20°C～+50°C; Relative humidity
range：15%～95%RH;
Handle with care and avoid heat, direct sunlight and water during
transportation
Expected Service Life
Five years
Software Version
UFR 1.1
Symbol Descriptions
The following symbols may appear in this manual, on the label, on the device or on accessories. Some of
the symbols represent standards and compliances associated with the device and its use.
WARNING: This alert identifies hazards that may cause serious personal injury or death
CAUTION: This alert identifies hazards that may cause minor personal injury, product
damage or property damage
Type BF applied part
Manufacturer
Specifies serial number
Authorised representative in the European Community
CE Mark: conforms to essential requirements of the Medical Device Directive 93/42/EEC
DISPOSAL: Do not dispose of this product as unsorted municipal waste. This product
should be treated as electronic waste
Direct current
Follow instructions for use

5
Important Safety Instructions
Before using this device, please read the following instructions with care.
WARNING:
•This thermometer is not intended to substitute for a consultation with your physician.
The forehead scan temperature serves as a reference only.
•Basic safety precautions should always be observed, especially when the
thermometer is used on or near children and disabled persons.
•Please place the device out of reach of children.
•Avoid using or leaving the device in direct sunlight or near radiant heat sources.
•Do not place the device in direct contact with the external environment (e.g close to
an external doorway).
•For the most accurate readings, individuals should acclimatise in the room where the
device is situated for 10-15 minutes.
•For best results, the device should be used in a location where room temperature is
20-25ºC.
•Do not touch the lens.
•Do not attempt to modify the device.
•The swallowing of small parts like packing bag, battery, battery cover and so on may
cause suffocation.
•There are no contraindications (use of this device does not pose a risk to individuals).
•The patrient is ther intended operator.
•Temperature reading is for reference only.
CAUTION:
•Please do not use a dilution agent, alcohol or petrol to clean the unit. Please use the
device with care.
•Please do not immerse the device in liquid.
•Please remove the batteries if you do not intend to use the device for more than
three months.
•Replace the batteries if the device shows a low battery symbol.
•Do not mix old and new batteries.
•Do not use the device during transportation.
Disposal
•Do not dispose of electrical appliances as unsorted municipal waste: use separate
collection facilities. Contact your local government for information. If electrical
appliances are disposed of in landfills or dumps, hazardous substances can leak into
groundwater.
Care and Maintenance
•Keep the device in its box when not in use, and store in a dry location.
•Clean the device with a soft, dry cloth. Do not use any abrasive cleaners.
•Never immerse the device in water.
•NOTE: The manufacturer/supplier will not be responsible for any quality or technical
issues that arise from improper use/maintenance as highlighted in this user manual.
Please note: Where prolonged use is expected, always power the device
from the mains using the Type C USB lead. The rechargeable battery
should only be used as back-up.

6
Parts Identification

7
Battery Installation
1. Remove the battery cover from the battery compartment.
2. Insert one 3.7V 18650 lithium battery, ensuring the battery is facing the correct way.
Positive (+) and Negative (-) are displayed on the back of the battery cover.
3. Replace the battery cover.
4. If the low battery symbol appears on the display, you will need to charge the battery
using the cable provided. To charge the battery, plug the cable into a USB
port/socket or use a USB plug. The device will need approximately eight hours to
reach full charge. A green strip will appear on the display during charging, changing
to a red strip when charging is complete.
Please note: Where prolonged use is expected, always power the device from
the mains using the Type C USB lead. The rechargeable battery should only be
used as back-up.
Battery Type
The UFR118 uses one 3.7V 18650 lithium-ion rechargeable battery. An 18650 battery has a
length of 65mm and a diameter of 18mm.
WARNING:
Dispose of batteries in accordance with local laws. To avoid explosion or fire, do not
burn or incinerate batteries.

8
About Normal Body Temperature and Fever
Forehead and temple area temperature differs from internal temperature, which can be taken
orally or rectally.
Vasoconstriction, an effect which constricts the blood vessels and cools the skin, can occur
during the early stages of a fever.
In this case, the temperature measured by the Infrared thermometer may be unusually low. If
the measurement therefore does not match the patient's own perception or is unusually low,
repeat the measurement every 15 minutes. As a reference, you can also measure the internal
body temperature using a conventional oral or rectal thermometer.
Body temperature can vary from one individual/person to next.
An individual’s temperature will also vary depending on location and time of day. The table
below shows the statistical normal ranges from different sites.
Please keep in mind that temperatures measured from different sites, even at the same time,
should not be directly compared. Fever indicates that the body temperature is higher than
normal. This symptom may be caused by infection, overdressing or immunisation. Some
people may not experience fever even when they are ill.
These include, but are not limited to, infants younger than 3 months old, individuals with
compromised immune systems, individuals taking antibiotics, steroids, or antipyretics (aspirin,
ibuprofen, acetaminophen), or individuals with certain chronic illnesses. Please consult your
physician when you feel ill even if you do not have fever.
Normal Temperatures According to Measurement
Method
Measurement Method
Normal Temp Range ºC
Normal Temp Range ºF
Rectal/Ear
36.6 to 38
97.8 to 100.4
Oral
35.5 to 37
95.9 to 98.6
Auxiliary
34.7 to 37.3
94.4 to 99.1
Note: Body Temperature at WebMD. Website:
http://firstaid.webmd.com/body-temperature; retrieved Jan 7 2010
The temperature of the human body can vary throughout the day. It can also be influenced
by numerous external factors.

9
Unit Setting
There is a small hole on the bottom of the device. Push a 2mm diameter screwdriver into the
hole to switch between ℃and ℉.
Operation
Please note: The device must be placed in the operating environment 30
minutes before use. Ensure it is not placed close to external doorways as this
may affect accuracy slightly. For more accurate results, individuals should be
in the same room as the device for 10-15 minutes prior to testing, and room
temperature should be 20-25ºC.
To use the thermometer, press the START/STOP button. All symbols will appear on the
display, and you will hear one short beep.
Stand in front of the device with a distance of 1cm –10cm between your forehead and the
sensor. The device will measure temperature automatically.
When measurement is complete, you will hear one long beep as the measurement appears
on the display.
The thermometer will automatically go into standby mode after 10 seconds of inactivity. If
motion is detected by the sensor, the device will power on again.

10
Beep Alarm
1. 1 short beep when power is on and device is ready to begin measurement.
2. 1 long beep with green LED when measurement reading is below 37.5℃/99.5℉.
3. 10 short beeps with red LED when measurement reading is 37.5℃/99.5℉or higher.
4. 3 short beeps with red LED if the device is unable to measure temperature.
•Babies' skin reacts very quickly to ambient temperature. Therefore, do not take their
temperature during/after breastfeeding as the skin temperature may be lower than
their internal body temperature.

11
Error Messages
Symbol
Explanation
In Body Mode, the measured temperature is above the
measuring range of 43℃/109.4℉.
In Body Mode, measured temperature is below the
measuring range of 32℃/89.6℉.
Low battery. Please connect the USB charger and
recharge the battery.
Thermometer has failed or is affected by electromagnetic
field.
LED light strip: when charging, illuminates green.
LED light strip: when charging is complete, illuminates red.
Warranty
•The device is guaranteed to be free of defects in workmanship and materials
under normal use for a period of 1 Year from the date of purchase.
•For repair under this warranty, our authorised service agent must be advised
of the fault within the period of the warranty. This warranty only covers parts
and labour service under normal operations. Any defect resulting from natural
causes, eg.flood, hurricane etc, is not covered in this guarantee. This
guarantee does not cover damage incurred by use of the unit not in
accordance with the instructions, accidental damage, or being tampered or
serviced by unauthorised service agents.
•The following will be excluded from this warranty: If the thermometer has been
misused, abused, or there has been neglect in following the manual's
instructions on purpose and unauthorised repair or modifications.
•The device requires no calibration.
•The device is not repairable and contains no user serviceable parts.

12
EMC Declaration
IEC 60601-1-2：2014 ME EQUIPMENT and ME SYSTEMS identification, marking and
documents for Class B product
Instructions for Use
The ME EQUIPMENT or ME SYSTEM is suitable for home healthcare environments.
Warning：Do not use near active HF surgical equipment and the RF shielded room of an ME system
for magnetic resonance imaging, where the intensity of EM disturbances is high.
Warning：Use of this equipment adjacent to or stacked with other equipment should be avoided
because it could result in improper operation. If such use is necessary, this equipment and the other
equipment should be observed to verify that they are operating normally.
Warning: Use of accessories, transducers and cables other than those specified or provided by the
manufacturer of this equipment could result in increased electromagnetic emissions or decreased
electromagnetic immunity of this equipment and result in improper operation.”
Warning：Portable RF communications equipment (including peripherals such as antenna cables and
external antennas) should be used no closer than 30 cm (12 inches) to any part of the thermometer,
including cables specified by the manufacturer. Otherwise, degradation of the performance of this
equipment could result.
If any：a list of all cables and maximum lengths of cables (if applicable), transducers and other
ACCESSORIES that are replaceable by the RESPONSIBLE ORGANIZATION and that are likely to
affect compliance of the ME EQUIPMENT or ME SYSTEM with the requirements of Clause 7
(EMISSIONS) and Clause 8 (IMMUNITY). ACCESSORIES may be specified either generically
(e.g. shielded cable, load impedance) or specifically (e.g. by MANUFACTURER and EQUIPMENT OR
TYPE REFERENCE).
If any：the performance of the ME EQUIPMENT or ME SYSTEM that was determined to be
ESSENTIAL PERFORMANCE and a description of what the OPERATOR can expect if the
ESSENTIAL PERFORMANCE is lost or degraded due to EM DISTURBANCES (the defined
term “ESSENTIAL PERFORMANCE” need not be used).

13
Technical description
1. All necessary instructions for maintaining BASIC SAFETY and ESSENTIAL PERFORMANCE
with regard to electromagnetic disturbances for the expected service life.
2. Guidance and manufacturer’s declaration - electromagnetic emissions and immunity.
Table 1
Guidance and manufacturer’s declaration - electromagnetic emissions
Emissions test
Compliance
RF emissions
CISPR 11
Group 1
RF emissions
CISPR 11
Class B
Harmonic emissions
IEC 61000-3-2
Class A
Voltage fluctuations/ flicker emissions
IEC 61000-3-3
Compliance

14
Table 2
Guidance and manufacturer’s declaration - electromagnetic Immunity
Immunity Test
IEC 60601-1-2
Test level
Compliance level
Electrostatic discharge (ESD)
IEC 61000-4-2
±8 kV contact
±2 kV, ±4 kV, ±8 kV, ±15 kV
air
±8 kV contact
±2 kV, ±4 kV, ±8 kV, ±15 kV air
Electrical fast transient/burst
IEC 61000-4-4
Power supply lines：±2 kV
100 kHz repetition
frequency
Power supply lines: ±2 kV 100 kHz
repetition frequency
Surge
IEC 61000-4-5
line(s) to line(s)：±1 kV.
line(s) to line(s)：±1 kV.
Voltage dips, short interruptions and
voltage variations on power supply
input lines
IEC 61000-4-11
0% 0.5 cycle
At 0º, 45 º, 90 º, 135 º, 180
º, 225 º, 270 º and 315 º
0% 1 cycle
And 70% 25/30 cycles
Single phase: at 0
0% 250 cycle (50Hz)
0% 0.5 cycle
At 0º, 45 º, 90 º, 135 º, 180 º, 225 º,
270 º and 315 º
0% 1 cycle
And 70% 25/30 cycles
Single phase: at 0
0% 250 cycle (50Hz)
Power frequency magnetic field
IEC 61000-4-8
30 A/m
50Hz/60Hz
30 A/m
50Hz/60Hz
Conduced RF
IEC61000-4-6
150KHz to 80MHz：
3Vrms
6Vrms (in ISM and amateur
radio bands)
80% Am at 1kHz
150KHz to 80MHz：
3Vrms
6Vrms (in ISM and amateur radio
bands)
80% Am at 1kHz
Radiated RF
IEC61000-4-3
10 V/m
80 MHz –2,7 GHz
80 % AM at 1 kHz
10 V/m
80 MHz –2,7 GHz
80 % AM at 1 kHz
NOTE UTis the a.c. mains voltage prior to application of the test level.

15
Table 3
Guidance and manufacturer’s declaration - electromagnetic Immunity
Radiated
RF
IEC61000-
4-3
(Test
specificatio
ns for
ENCLOSU
RE PORT
IMMUNITY
to
RF wireless
communicat
ions
equipment)
Test
Frequency
(MHz)
Band
(MHz)
Service
Modulation
Modulation
(W)
Distance
(m)
IMMUN
ITY
TEST
LEVEL
(V/m)
385
380 –390
TETRA 400
Pulse
modulation
18 Hz
1,8
0.3
27
450
430 –470
GMRS 460,
FRS 460
FM
± 5 kHz
deviation
1 kHz sine
2
0.3
28
710
704 –
787
LTE Band
13,
17
Pulse
modulation
217 Hz
0,2
0.3
9
745
780
810
800 –
960
GSM
800/900,
TETRA
800,
iDEN 820,
CDMA 850,
LTE Band 5
Pulse
modulation
18 Hz
2
0.3
28
870
930
1720
1 700 –
1 990
GSM 1800;
CDMA
1900;
GSM 1900;
DECT;
LTE Band
1, 3,
4, 25;
UMTS
Pulse
modulation
217 Hz
2
0.3
28
1845
1970
2450
2 400 –
2 570
Bluetooth,
WLAN,
802.11
b/g/n,
RFID 2450,
LTE Band 7
Pulse
modulation
217 Hz
2
0.3
28
5240
5 100 –
5 800
WLAN
802.11
a/n
Pulse
modulation
217 Hz
0,2
0.3
9

16
[phone]
[e-mail]
Distribution:
Unit 7, Centurion Business Park,
Coggin Mill Way,
Rotherham,
S60 1FB
Head Office:
Unit 1, Genesis Business Park,
Sheffield Road,
Rotherham
S60 1DX
www.marsden-weighing.co.uk