FORA IR42-1242A Non Contact Forehead Thermometer Instruction Manual
- June 6, 2024
- FORA
Table of Contents
- FORA IR42-1242A Non Contact Forehead Thermometer
- INTRODUCTION
- APPEARANCE AND KEY FUNCTIONS OF THE THERMOMETER
- LCD SCREEN
- IMPORTANT SAFETY INSTRUCTIONS
- USING THE DEVICE
- RECALLING PAST READINGS
- MAINTENANCE
- CLEANING AND DISINFECTION
- SYMBOL INFORMATION
- TROUBLESHOOTING
- SPECIFICATIONS
- WARRANTY TERMS AND CONDITIONS
- Read User Manual Online (PDF format)
- Download This Manual (PDF format)
FORA IR42-1242A Non Contact Forehead Thermometer
ForaCare Suisse AG
Neugasse 55,
9000, St. Gallen,
Switzerland
www.foracare.ch
INTRODUCTION
Thank you for choosing FORA FocusTemp Forehead Thermometer. Please read this instruction manual first so that the thermometer can be used safely and correctly. Keep this instruction manual for future reference. This innovative medical device uses advanced infrared (IR) technology to measure temperature instantly and accurately on the forehead/any surface area. FORA FocusTemp Forehead Thermometer delivers a body temperature reading from the thermal radiation emitted from the forehead without any body contact.
INTENDED USE
FORA FocusTemp Forehead Thermometer is intended for the intermittent
measurement and monitoring of human body temperature from the forehead. The
device is intended for use by people of all ages in the home or by healthcare
professionals.
APPEARANCE AND KEY FUNCTIONS OF THE THERMOMETER
1. Probe lens
2. Display screen
3. Power/ Measure button
4. Protective sensor cap
5. Mode button
6. Memory button
7. Battery Cover
LCD SCREEN
- Adult body temperature indicator
- Child body temperature indicator
- Object surface temperature indicator
- Error message
- Memory mode
- Hold Symbol
- Battery indicator
- Temperature display
- Temperature unit
IMPORTANT SAFETY INSTRUCTIONS
READ THIS BEFORE USING AND KEEP THESE INSTRUCTIONS IN A SAFE PLACE
- Close supervision is necessary when the thermometer is used by, on, or near children, handicapped persons or invalids.
- Use the thermometer only for the intended use described in this manual.
- Do not use the thermometer if it is not working properly, or if it has sustained any damage.
- Keep the sensor end clean and free of debris. See Maintenance section for instructions.
- Do not use ethylene oxide gas, heat, autoclave, or any other harsh methods to sterilize the device.
- Put in place the protective sensor cap on the sensor end when not in use.
- Do not use the device shortly after exercise, bathing or coming indoors.
- If coming from an environment of warmer or cooler temperature or after a period of exertion, allow the user and the thermometer to reach room temperature for 20 minutes prior to taking a measurement.
- As the forehead temperature may be affected by sweat, oil and the surrounding temperature, the reading shall be taken as a reference only.
- Do not use in presence of flammable anesthetic mixtures.
- Do not use accessories which are not supplied or recommended by the manufacturer.
- Proper maintenance is essential to the longevity of your device. If you are concerned about the accuracy of measurement, please contact the local customer service or place of purchase for assistance.
WARNING AND PRECAUTIONS
- As with any thermometer, proper technique is crucial to getting accurate temperature readings. Please read this manual thoroughly and carefully before use.
- Always operate the thermometer in an operating temperature range 10°C to 40°C, and relative humidity of less than 85%.
- Always store the thermometer in a cool and dry place: temperatures between -20°C to 60°C; relative humidity less than 85%. Avoid direct sunlight.
- Avoid dropping the thermometer.
- Basic safety precautions should always be observed, especially when the thermometer is used on or near children and disabled persons.
- This thermometer is not intended to be a substitution for a consultation with your physician.
USING THE DEVICE
Install Battery
- Remove the battery cover by pressing down at the arrow mark and slide to the direction of the arrow as shown in the figures below.
- Install (2) AAA alkaline batteries and close the battery cover.
- Remove the batteries if the thermometer is stored and not in use.
MEASUREMENT MODES
The default measuring mode is for the adult forehead temperature. Press the MODE button on the side of the thermometer to adjust the measuring mode.
MEASURING TEMPERATURE FOR ADULTS
- Remove the protective cap. The forehead should be clear of hair and perspiration.
- Aim at the center of the forehead area 3 to 7cm away from and perpendicular to the surface of the skin.
- Press and release the Measure button to take a measurement. A double “beep” sound indicates that a reading has been taken and displayed on the LCD screen.When a reading is more than 38°C, a warning symbol will flash with a red backlight.
- To take another measurement, follow steps 2 and 3.
- The thermometer turns off automatically after 30 seconds. Replace the sensory cap when finished.
WARNING AND PRECAUTIONS
- If the reading is < 31.9°C, “Lo” will be displayed.
- If the reading is ≥ 32.0°C and ≤ 37.9 °C, it will be displayed with a green backlight.
- If the reading is ≥ 38°C and ≥ 43°C, it will be displayed with a red backlight.
- If the reading is ≥ 43.1°C, “Hi” will be displayed.
MEASURING TEMPERATURE FOR CHILDREN
- Press the Power button to turn on the thermometer.
- Press and hold the MODE button for 1 second before releasing. An adult facial profile should be flashing, indicating that the preset mode is for adults.
- Press the MODE key to switch to Child mode which is indicated by a smiley face icon.
- Aim the scanner at the center of the child’s forehead 3 to 7cm away from and perpendicular to the surface of the skin. Press and release the Measure button to take a measurement. A red backlight with a warning symbol indicates a reading more than 37.6 °C.
- The thermometer will be switched off automatically when left idle for 30 seconds.
- Replace the sensor cap when finished.
Note:
- If the reading is ≤ 31.9°C, “Lo” will be displayed.
- If the reading is ≥ 32°C and ≤ 37.6 °C, it will be displayed with a green backlight.
- If the reading is ≥ 37.7 °C and ≤ 43°C, it will be displayed with a red backlight.
- If the reading is ≥ 43.1°C, “Hi” will be displayed.
- Parents should not rely only on temperature readings. If you have concerns, please seek medical advice.
MEASURING SURFACE TEMPERATURE
- Press the Power button to turn on the thermometer.
- Press and hold the MODE button for 1 second before releasing. An adult facial profile should be flashing, indicating that the preset mode is for adults.
- Press the MODE key to switch to Surface mode which is indicated by a thermometer icon.
- Make sure the probe is flat and close to the surface of the object and not at an angle. The measurement should be taken within a distance of 5 cm. Press and hold the Measure button as you move the meter along the surface. The HOLD symbol flashes.
- Release the button and read the result. If the reading is ≥ 0°C and ≤ 100.1°C, it will be displayed with a green backlight.
Note:
- If the reading is ≤ 0°C, “Lo” will be displayed.
- If the reading is ≥ 100.1°C, “Hi” will be displayed.
RECALLING PAST READINGS
FORA FocusTemp stores 30 of the most recent readings.
- Press and release the Power button to turn on the thermometer.
- Press and hold the MEMORY button for 1 second to enter the memory mode which is indicated by a flashing ” ” symbol. The most recent reading which is stored will be displayed.
- Press and release the MEMORY button to scroll through older readings.
- When left idle for 30 seconds, the thermometer will be switched off automatically.
Note: When the memory is full, the oldest result deleted as the new ones are added. While recalling previous readings, you may take a measurement by pressing the Measure button.
ABOUT NORMAL BODY TEMPERATURE & FEVER
Body temperature can vary from one individual person to the next. It also
varies according to the location on the body and time of day. Fever indicates
that the body temperature is higher than normal. This symptom may be caused by
infection, overdressing or immunization. Some people may not experience fever
even when they are ill. These include, but are not limited to, infants younger
than 3 months old, persons with compromised immune systems, persons taking
antibiotics, steroids or antipyretics
(aspirin, ibuprofen, acetaminophen), or persons with certain chronic
illnesses. Please consult your physician if you are concerned about your body
temperature readings.
MAINTENANCE
- FORA FocusTemp has no user serviceable internal parts except for the battery replacement.
- Always replace the Sensor Cap (or place in cradle) when not in use.
- Store in a dry location free of dust and away from direct sunlight.
CLEANING AND DISINFECTION
- Use a soft dry cloth to clean the plastic casing or a cloth dampened with a solution of water and mild detergent. Occasionally, 70% isopropanol solution may be used. Never submerge in liquid.
- The sensor window is recessed to assist in keeping it clean and free of debris. Inspect the lens and remove any debris. Smudges may be cleaned by gently wiping the window with a small foam-tipped swab (non-linting) moistened with 70% alcohol. Wait 10 minutes prior to taking your temperature.
SYMBOL INFORMATION
TROUBLESHOOTING
SPECIFICATIONS
Model No.: | FORA IR42a |
---|---|
Dimension & Weight | 155.46 (L) x 40.14 (W) x 39.45 (H) mm, |
61.8g (without battery)
Power Source| 2 x 1.5V AAA alkaline batteries
Battery Life| With new batteries, approx. 5,000 measurements.
Displayed Temperature range| • Forehead: 32°C to 43°C
• Object Surface: 0°C to 100°C
Display Resolution| 0.1°C
Accuracy| The accuracy requirements specified in ASTM E1965-98 is met
• Forehead: ±0.2°C for the range of 35.0°C to 42.0°C / ±0.3°C for the range of <35.0°C or >42.0°C
• Object surface: ±1°C
Reference to Standards| ASTM E1965-98; IEC 60601-1; IEC 60601-1-2 (EMC)
Temperature Unit| °C
Operating Temperature Range| 10°C to 40°C
Operating Humidity| 85% RH or less
Storage / Transportation Temperature Range| -20°C to 60°C
Storage / Transportation Humidity| 85% RH or less
Memory Capacity| 30 measurements
Calibration method| Oral calibration/ sublingual
WARRANTY TERMS AND CONDITIONS
With respect to disposable products, ForaCare Suisse warrants to the original purchaser that, at time of delivery, each standard product manufactured by ForaCare Suisse shall be free from defects in material and workmanship and, when used for the purposes and indications described on the labeling, is fit for the purposes and indications described on the labeling. All warranties for a product shall expire as of the product expiration date, or if none, after two (2) years from the original date of purchase, as long as it has not been modified, altered, or misused. ForaCare Suisse warranty hereunder shall not apply if:
(i) a product is not used in accordance with its instructions or if it is used for a purpose not indicated on the labeling; (ii) any repairs, alterations or other work has been performed by the buyer or others on such item, other than work performed with ForaCare Suisse’s authorisation and according to its approved procedures; or (iii) the alleged defect is a result of abuse, misuse, improper maintenance, accident or the negligence of any party other than ForaCare Suisse. The warranty set forth herein is conditioned upon proper storage, installation, use and maintenance in accordance with applicable written recommendations from ForaCare Suisse.
The warranty furnished hereunder does not extend to damaged items purchased hereunder resulting in whole or in part from the use of components, accessories, parts or supplies not furnished by ForaCare Suisse.
Warning: Medical electrical equipment needs special precautions regarding
EMC and needs to be installed according to the EMC information provided.
Careful consideration of this information is essential when stacking or
collocating equipment and when routing cables and accessories.
Warning: RF mobile communications equipment can affect medical electrical
equipment.
Recommended separation distance between portable and mobile RF communications equipment and the FocusTemp
The FocusTemp is intended for use in an electromagnetic environment (for home
healthcare and professional healthcare) in which radiated RF disturbances are
controlled. The customer or the user of the FocusTemp can help prevent
electromagnetic interference by maintaining a minimum distance between the
portable and mobile RF communications equipment (transmitters) and the
FocusTemp as recommended below, depending on the maximum output power of the
communications equipment.
Rated maximum output power of transmitter
W
| Separation distance according to frequency of transmitter
m
150 kHz to 80 MHz
d =1,2√P
| 80 MHz to 800 MHz
d =1,2√P
| 800 MHz to 2,7
GHz
d =2,3√P
0,01| N/A| 0,12| 0,23
0,1| N/A| 0,38| 0,73
1| N/A| 1,2| 2,3
10| N/A| 3,8| 7,3
100| N/A| 12| 23
For transmitters rated at a maximum output power not listed above, the
recommended separation distance d in meters (m) can be estimated using the
equation applicable to the frequency of the transmitter, where p is the
maximum output power rating of the transmitter in watts (W) depending on the
transmitter manufacturer.
Note 1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
Note 2 These guidelines may not apply to all situations. Electromagnetic
propagation is affected by absorption and reflection from structures, objects
and people.
Manufacturer’s declaration-electromagnetic emissions
The FocusTemp is intended for use in the electromagnetic environment (for home healthcare and professional healthcare) specified below.
The customer or the user of the FocusTemp should assure that it is used in such an environment.
Emission test| Compliance| Electromagnetic environment-guidance
(for home healthcare and professional healthcare)
RF-emissies CISPR 11| Group 1| The FocusTemp uses RF energy only for internal
use. Therefore, its RF emissions are very low and are not likely to cause any
interference from nearby electronic equipment.
RF-emissies CISPR 11| Class B| The FocusTemp is suitable for use in all
establishments, including domestic establishments and those directly connected
to the public low-voltage power supply network that supplies buildings used
for domestic purposes.
Harmonic emissions IEC 61000-3-2| Not applicable
Voltage fluctuations
/flicker emissions IEC 61000-
3-3
| Not applicable
Manufacturer’s declaration-electromagnetic immunity
The FocusTemp is intended for use in the electromagnetic environment (for home
healthcare and professional healthcare) specified below.
The customer or the user of the FocusTemp should assure that it is used in the
environment specified below.
Immunity test| IEC 60601
test level
| Compliance level| Electromagnetic environment- guidance (for home
healthcare and professional healthcare environment)
Electrostatic discharge(ESD) IEC 61000-4-2| Contact:±8 kV Air±2 kV,±4 kV,±8
kV,±15 kV| Contact:±8 kV Air±2 kV,±4 kV,±8 kV,±15 kV| Floors should be wood,
concrete or ceramic tile. If
floors are covered with synthetic material, the relative humidity should be at least
30%.
Electrical fast transient/burst IEC 61000-4-4| ± 2kV for power supply lines
± 1kV for input/ output lines
| Not applicable
Not applicable
| Mains power quality should be that of a typical home healthcare and
professional healthcare environment.
---|---|---|---
Surge IEC 61000-
4-5
| ± 0.5kV, ±1kV
line(s) to line(s)
± 0.5kV, ±1kV,± 2kV
line(s) to earth
| Not applicable
Not applicable
| Mains power quality should be that of a typical home healthcare and
professional healthcare environment.
Voltage Dips, short interruptions and voltage variations on power supply input
lines IEC 61000-4-11| Voltage dips:
0 % UT ; 0,5 cycle 0
% UT ; 1 cycle 70 % UT ; 25/30
cycles
Voltage interruptions:
0 % UT ; 250/300
cycle
| Voltage dips: Not applicable Not applicable Not applicable
Voltage interruptions: Not applicable
| Mains power quality should be that of a typical home healthcare and professional healthcare environment.
If the user of the FocusTemp requires continued operation during power mains interruptions, it
is recommended that the FocusTemp be powered from an uninterruptible power supply or a battery.
Power frequency(50, 60 Hz) magnetic field IEC 61000-4-8| 30 A/m
50 Hz or 60 Hz
| 30 A/m
50 Hz and 60 Hz
| The FocusTemp power frequency magnetic
fields should
be at levels characteristic of a typical location in a typical home healthcare and professional healthcare environment.
NOTE: UT is the a.c. mains voltage prior to application of the test level.
Manufacturer’s declaration-electromagnetic immunity
The FocusTemp is intended for use in the electromagnetic environment (for home healthcare and professional healthcare) specified below.
The customer or the user of the FocusTemp should assure that it is used in the environment specified below.
Immunity test| IEC 60601
test level
| Compliance level| Electromagnetic environment- guidance (for home healthcare
and professional healthcare environment)
Conducted RF
IEC 61000-
4-6
Radiated RF
IEC 61000-
4-3
| 3 Vrms:
0,15 MHz –
80 MHz
6 Vrms:
in ISM and amateur radio bands between 0,15 MHz
and 80 MHz
80 % AM at
1 kHz
10 V/m
80 MHz –
2,7 GHz
80 % AM at
1 kHz
| Not applicable Not applicable
10 V/m
80 MHz – 2,7
GHz
80 % AM at 1
kHz
| Portable and mobile RF communications equipment must not be used close to any parts of the FocusTemp including cables, other than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter.
Recommended separation distance:
d = 1,2 √P
d = 1,2 √P 80MHz to 800 MHz d = 2,3 √P 800MHz to 2,7 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 fixed RF transmitters, as determined by an electromagnetic site survey, a should be less than the compliance level in each frequency range.b
| | | Interference may occur in the vicinity of equipment marked with the
following symbol:
Note 1 At 80 MHz and 800 MHz, the higher frequency range applies.
Note 2 These guidelines may not apply to all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.
- Field strengths from fixed 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 fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the FocusTemp is used exceeds the applicable RF compliance level above, the FocusTemp should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as re-orienting or relocating the FocusTemp.
- Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
Manufacturer’s declaration-electromagnetic immunity
Test specifications for ENCLOSURE PORT IMMUNITY to RF wireless
communications equipment
The FocusTemp is intended for use in the electromagnetic environment (for home healthcare and professional healthcare) specified below.
Test frequency (MHz)| Band a)
(MHz
| Service a)| Modulation
b)
| Maximum power (W)| Distance (m)| IMMUNITY TEST LEVEL
(V/m)
| Compliance LEVEL
(V/m)
(for home and professional healthcare)
385
|
380
–390
|
TETRA 400
| Pulse modulation
b)
18 Hz
|
1,8
|
0,3
|
27
|
27
450
|
430 –
470
|
GMRS 460,
FRS 460
| FM c)
±5 kHz deviation 1 kHz sine
|
2
|
0,3
|
28
|
28
710|
704 –
787
| LTE Band 13,
17
| Pulse modulation
b)
217 Hz
| 0,2| 0,3| 9| 9
745
780
810|
800 –
960
| GSM 800/900, TETRA 800,
iDEN 820,
CDMA 850,
LTE Band 5
|
Pulse modulation
b)
18 Hz
| 2| 0,3| 28| 28
870
930
1 720|
1 700 –
1 990
| GSM 1800; CDMA 1900;
GSM 1900; DECT;
LTE Band 1, 3,
4, 25;
UMTS
|
Pulse modulation
b)
217 Hz
| 2| 0,3| 28| 28
1 845
1 970
2 450| 2 400 –
2 570
| Bluetooth, WLAN,
802.11 b/g/ n,
RFID 2450,
LTE Band 7
|
Pulse modulation
b)
217 Hz
| 2| 0,3| 28| 28
5 240|
5 100 –
5 800
| WLAN 802.11
a/n
| Pulse modulation
b)
217 Hz
|
0,2
|
0,3
|
9
|
9
5 500
5 785
NOTE To achieve the IMMUNITY TEST LEVEL, the distance between the
transmitting antenna and the ME EQUIPMENT or ME SYSTEM may be reduced to 1 m.
The 1 m test distance is permitted by IEC 61000-4-3.
a) For some services, only the uplink frequencies are included.
b) The carrier shall be modulated using a 50 % duty cycle square wave signal.
c) As an alternative to FM modulation, 50 % pulse modulation at 18 Hz may be used because while it does not represent actual modulation, it would be the worst case.
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