Warning
Do not use the thermometer under temperature extremes (below
16˚C/60.8˚F or over 35˚C/95˚F) or humidity extremes (below 15%RH
or over 80%RH).
*Failing to do so may cause inaccuracy.
Do not expose the thermometer to temperature extremes (below
-20˚C/-4˚F or over 55˚C/131˚F) or humidity extremes (below 15%RH
or over 93%RH).
*Failing to do so may cause inaccuracy.
Temperature probe has been shocked and lax.
*Contact MHC Medical Products immediately.
It is dangerous for patients to perform a self-evaluation and
self-treatment based on the measuring results. Be sure to follow
doctors’ instruction.
*A self-evaluation may cause a disease to worsen.
Don’t touch or blow infrared sensor.
*A contaminated or broken infrared sensor may cause inaccuracy.
Clean a contaminated infrared sensor with a soft dry cloth in a
gentle manner.
*Cleaning with toilet tissue or paper towel may scratch the infrared
sensor, causing inaccuracy.
Install the battery in the right position according to the manual.
*Incorrect replacement will cause battery heat.
Do not immerse the thermomter in liquids.
*This instrument is not waterproof.
Do not use a mobile phone nearby when the thermometer is
working.
*Portable and mobile RF communications equipment can affect
MEDICAL ELECTICAL EQUIPMENT. Falling to do so may cause
inaccuracy.
The probe glass is made from special material which is not easy
broken.
*If there is any damage, stop using it and contact MHC Medical
Products immediately.
Do not modify this equipment without authorization of the
manufacturer.
*Contact MHC Medical Products immediately.
The device is not repairable and contains no user serviceable parts.
*If there is any problem, contact MHC Medical Products immediately.
The device requires no calibration.
*If there is any problem, contact MHC Medical Products immediately.
No modification of this equipment is allowed.
*If there is any problem, contact MHC Medical Products immediately.
If this equipment is modified, appropriate inspection and testing
must be conducted to ensure continued safe use of the equipment.
*If there is any problem, contact MHC Medical Products immediately.
The operator shall not touch the thermometer and the patient
simultaneously.
Keep the machine out of children’s reach.
*For accidental swallow of battery of protective film, please consult
the doctor at once.
For temperature difference between storage area and measurement
site, condition the thermometer for about 30 minutes in room
temperature (measurement site).
*Failing to do so may cause inaccuracy.
Ensure that children do not use the instrument unsupervised.
*some parts are small enough to be swallowed.
Error Messages
Error
Message
Problem
Solution
Hi
Temperature is
higher than 42.2˚C
(108˚F).
Operate the thermometer only
between the specified temperature
ranges. In the event of a repeated
error message, contact MHC
Medical Products.
Lo
Temperature is
lower than 32˚C
(89.6˚F).
Operate the thermometer only
between the specified temperature
ranges. In the event of a repeated
error message, contact MHC
Medical Products.
Err
Sensor not welded Contact MHC Medical Products.
Low power
Replace with new batteries
ErH
The temperature
of the measuring
environment is
too high.
Decrease the temperature of
the environment, keep it within
60.8˚F-95˚F (16˚C-35˚C).
ErL
The temperature
of the measuring
environment is
too low
Increase the tmperature of the
environment, keep it within
60.8˚F-95˚F (16˚C-35˚C).
Maintenance, storage and calibration
Maintenance:
1. Gently remove any dirt on the body using a soft and
dry cloth.
2. Use a cotton swab or soft cloth absorbed with alcohol, and
gently wipe the lens of the temperature measuring head.
After using the product, the product can be sterilized with
70% medical alcohol on the soft towel or cotton sliver. If the
probe tip is damaged, please contact MHC Medical Products.
3. Don’t wash with water or detergent containing abrasive or
benzene.
4. Do not immerse in liquids.
Storage:
1. The device must not be stored or used in locations that are
excessively high or low temperature or humidity, in direct
sunlight, or in close proximity to an electrical current or in
dusty locations. Otherwise inaccuracies may occur.
2. Remove the battery if the thermometer is not used for
longer than one month.
Calibration:
This thermometer is calibrated at the time of manufacture.
If the thermometer is used according to the instruction,
periodic recalibration is not required. If at any time you
question the accuracy of the measurement, please contact
MHC Medical Products immediately.
Don’t attempt to modify or reassemble the thermometer.
Technical Specifications
Parameter
Specification
Measurement Mode
Forehead mode
Measurement Units
Fahrenheit (˚F) and Celsius (˚C)
Operating
Conditions
60.8˚F to 95˚F (16˚C-35˚C) with a relative
humidity of 15%-80%
Storage Conditions
-4˚F to 131˚F (-20˚C-+55˚C) with a relative
humidity of 15%-93%
Measurement
Distance
0.59” to 1.97” (15mm to 50mm) from the
measuring point
Forehead
temperature
measurement range
and accuracy
Measurement range: 89.6˚F-108˚F
(32.0˚C-42.2˚C)
Measurement accuracy: ±0.4˚F
(95.0˚F-107.6˚F)\±0.2˚C (35.0˚C-42.0˚C);
±0.5˚F (±0.3˚C) other range.
Memories recall
32 measurement recall
Dimensions
5.9” x 1.46” x 0.64” (150mmx37mmx16.3mm)
Weight
51g without batteries
Battery
2xAAA batteries (DC.3V)
Switch off
Automatically switches off after 1 minute
Product life
5 years
New battery life
1000 times
Standard
The product is made under the ISO80601-2-56.
Guarantee
Two-year warranty is available from purchasing date, excluding
user-caused failures listed below:
1. Failure resulted in unauthorized disassembly and
modification.
2. Failure resulted in unexpected drop during application or
transportation.
3. Failure resulted in operation away from proper instruction in
User’s Manual.
Included in delievery
• Infrared thermometer
• Instructions for use
• 2 x AAA batteries
Distributed by MHC Medical Products, LLC.
8695 Seward Road, Fairfield, OH 45011
Tel: (877) 358.4342
Email: info@MHCmed.com
Website: MHCmed.com
Manufactured by Alicn Medical Shenzhen, Inc.
4/F, B Building, Shenfubao Modern Optical Factory,
Kengzi Street, Pingshan District, 518122, Shenzhen City,
PEOPLE’S REPUBLIC OF CHINA
Electromagnetic Compatibility
The ME EQUIPMENT or ME SYSTEM is suitable for home
healthcare and hospital environments.
Warning: Do not use near active HF (high-frequency) 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.
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).
1. All necessary instructions for maintaining BASIC SAFETY and
ESSENTIAL PERFORMANCE with regard to electromagnetic
disturbances for the excepted service life.
2. Guidance and manufacturer’s declaration -electromagnetic
emissions and Immunity.
Table 1
Guidance and manufacturer’s declaration –
electromagnetic emission
Emmisions Test
Compliance
RF emissions
CISPR 11
Group 1
RF emissions
CISPR11
Class B
Harmonic emissions
IEC 61000-3-2
N/A
Voltage fluctuations/flicker emissions
IEC 61000-3-3
N/A
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
input/output lines:
±1 kV
N/A
Surge
IEC 61000-4-5
line(s) to line(s): ±1 kV
line(s) to earth: ±2 kV
100 kHz repetition
frequency
N/A
Voltage dips, short
interruptions and
voltage variations on
power supply input
lines.
IEC 61000-4-11
0% 0.5 cycle
At 0˚, 45˚, 90˚, 135˚,
180˚, 225˚, 270˚,
and 315˚
0% 1 cycle
And
70% 25/30 cycles
Singel phase: at 0
0% 300 cycle
N/A
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
N/A
Radiated RF
IEC 61000-4-3
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 U
T
is the a.c. mians voltage prior to application of the test level.
Table 3
Guidance and manufacturer’s declaration - electromagnetic Immunity
Radiated RF
IEC61000-4-3
(Test
specifications
for ENCLOSURE
PORT IMMUNITY
to RF wireless
communications
equipment)
Test
Frequency
(MHz)
Band
(MHz)
Service
Modulation
Modulation
(W)
Distance
(m)
IMMUNITY
TEST LEVEL
(V/m)
385
380–
390
TETRA
400
Pulse
modulation
18 Hz
1,8
0.3
27
450
380–
390
GMRS
460,
FRS
460
FM
± 5 kHz
deviation
1kHz 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
1700–
1990
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
2400–
2570
Bluetooth,
WLAN,
802.11
b/g/n,
RFID
2450,
LTE
Band 7
Pulse
modulation
217 Hz
2
0.3
28
5240
5100–
5800
WLAN
802.11
a/n
Pulse
modulation
217 Hz
0,2
0.3
9
5240
5785
6
7
8
9
10
Version: 1.0
Date modified: 2020-04-17
AD-102620.1
Warning
Do not use the thermometer under temperature extremes (below
16˚C/60.8˚F or over 35˚C/95˚F) or humidity extremes (below 15%RH
or over 80%RH).
*Failing to do so may cause inaccuracy.
Do not expose the thermometer to temperature extremes (below
-20˚C/-4˚F or over 55˚C/131˚F) or humidity extremes (below 15%RH
or over 93%RH).
*Failing to do so may cause inaccuracy.
Temperature probe has been shocked and lax.
*Contact MHC Medical Products immediately.
It is dangerous for patients to perform a self-evaluation and
self-treatment based on the measuring results. Be sure to follow
doctors’ instruction.
*A self-evaluation may cause a disease to worsen.
Don’t touch or blow infrared sensor.
*A contaminated or broken infrared sensor may cause inaccuracy.
Clean a contaminated infrared sensor with a soft dry cloth in a
gentle manner.
*Cleaning with toilet tissue or paper towel may scratch the infrared
sensor, causing inaccuracy.
Install the battery in the right position according to the manual.
*Incorrect replacement will cause battery heat.
Do not immerse the thermomter in liquids.
*This instrument is not waterproof.
Do not use a mobile phone nearby when the thermometer is
working.
*Portable and mobile RF communications equipment can affect
MEDICAL ELECTICAL EQUIPMENT. Falling to do so may cause
inaccuracy.
The probe glass is made from special material which is not easy
broken.
*If there is any damage, stop using it and contact MHC Medical
Products immediately.
Do not modify this equipment without authorization of the
manufacturer.
*Contact MHC Medical Products immediately.
The device is not repairable and contains no user serviceable parts.
*If there is any problem, contact MHC Medical Products immediately.
The device requires no calibration.
*If there is any problem, contact MHC Medical Products immediately.
No modification of this equipment is allowed.
*If there is any problem, contact MHC Medical Products immediately.
If this equipment is modified, appropriate inspection and testing
must be conducted to ensure continued safe use of the equipment.
*If there is any problem, contact MHC Medical Products immediately.
The operator shall not touch the thermometer and the patient
simultaneously.
Keep the machine out of children’s reach.
*For accidental swallow of battery of protective film, please consult
the doctor at once.
For temperature difference between storage area and measurement
site, condition the thermometer for about 30 minutes in room
temperature (measurement site).
*Failing to do so may cause inaccuracy.
Ensure that children do not use the instrument unsupervised.
*some parts are small enough to be swallowed.
Error Messages
Error
Message
Problem
Solution
Hi
Temperature is
higher than 42.2˚C
(108˚F).
Operate the thermometer only
between the specified temperature
ranges. In the event of a repeated
error message, contact MHC
Medical Products.
Lo
Temperature is
lower than 32˚C
(89.6˚F).
Operate the thermometer only
between the specified temperature
ranges. In the event of a repeated
error message, contact MHC
Medical Products.
Err
Sensor not welded Contact MHC Medical Products.
Low power
Replace with new batteries
ErH
The temperature
of the measuring
environment is
too high.
Decrease the temperature of
the environment, keep it within
60.8˚F-95˚F (16˚C-35˚C).
ErL
The temperature
of the measuring
environment is
too low
Increase the tmperature of the
environment, keep it within
60.8˚F-95˚F (16˚C-35˚C).
Maintenance, storage and calibration
Maintenance:
1. Gently remove any dirt on the body using a soft and
dry cloth.
2. Use a cotton swab or soft cloth absorbed with alcohol, and
gently wipe the lens of the temperature measuring head.
After using the product, the product can be sterilized with
70% medical alcohol on the soft towel or cotton sliver. If the
probe tip is damaged, please contact MHC Medical Products.
3. Don’t wash with water or detergent containing abrasive or
benzene.
4. Do not immerse in liquids.
Storage:
1. The device must not be stored or used in locations that are
excessively high or low temperature or humidity, in direct
sunlight, or in close proximity to an electrical current or in
dusty locations. Otherwise inaccuracies may occur.
2. Remove the battery if the thermometer is not used for
longer than one month.
Calibration:
This thermometer is calibrated at the time of manufacture.
If the thermometer is used according to the instruction,
periodic recalibration is not required. If at any time you
question the accuracy of the measurement, please contact
MHC Medical Products immediately.
Don’t attempt to modify or reassemble the thermometer.
Technical Specifications
Parameter
Specification
Measurement Mode
Forehead mode
Measurement Units
Fahrenheit (˚F) and Celsius (˚C)
Operating
Conditions
60.8˚F to 95˚F (16˚C-35˚C) with a relative
humidity of 15%-80%
Storage Conditions
-4˚F to 131˚F (-20˚C-+55˚C) with a relative
humidity of 15%-93%
Measurement
Distance
0.59” to 1.97” (15mm to 50mm) from the
measuring point
Forehead
temperature
measurement range
and accuracy
Measurement range: 89.6˚F-108˚F
(32.0˚C-42.2˚C)
Measurement accuracy: ±0.4˚F
(95.0˚F-107.6˚F)\±0.2˚C (35.0˚C-42.0˚C);
±0.5˚F (±0.3˚C) other range.
Memories recall
32 measurement recall
Dimensions
5.9” x 1.46” x 0.64” (150mmx37mmx16.3mm)
Weight
51g without batteries
Battery
2xAAA batteries (DC.3V)
Switch off
Automatically switches off after 1 minute
Product life
5 years
New battery life
1000 times
Standard
The product is made under the ISO80601-2-56.
Guarantee
Two-year warranty is available from purchasing date, excluding
user-caused failures listed below:
1. Failure resulted in unauthorized disassembly and
modification.
2. Failure resulted in unexpected drop during application or
transportation.
3. Failure resulted in operation away from proper instruction in
User’s Manual.
Included in delievery
• Infrared thermometer
• Instructions for use
• 2 x AAA batteries
Distributed by MHC Medical Products, LLC.
8695 Seward Road, Fairfield, OH 45011
Tel: (877) 358.4342
Email: info@MHCmed.com
Website: MHCmed.com
Manufactured by Alicn Medical Shenzhen, Inc.
4/F, B Building, Shenfubao Modern Optical Factory,
Kengzi Street, Pingshan District, 518122, Shenzhen City,
PEOPLE’S REPUBLIC OF CHINA
Electromagnetic Compatibility
The ME EQUIPMENT or ME SYSTEM is suitable for home
healthcare and hospital environments.
Warning: Do not use near active HF (high-frequency) 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.
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).
1. All necessary instructions for maintaining BASIC SAFETY and
ESSENTIAL PERFORMANCE with regard to electromagnetic
disturbances for the excepted service life.
2. Guidance and manufacturer’s declaration -electromagnetic
emissions and Immunity.
Table 1
Guidance and manufacturer’s declaration –
electromagnetic emission
Emmisions Test
Compliance
RF emissions
CISPR 11
Group 1
RF emissions
CISPR11
Class B
Harmonic emissions
IEC 61000-3-2
N/A
Voltage fluctuations/flicker emissions
IEC 61000-3-3
N/A
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
input/output lines:
±1 kV
N/A
Surge
IEC 61000-4-5
line(s) to line(s): ±1 kV
line(s) to earth: ±2 kV
100 kHz repetition
frequency
N/A
Voltage dips, short
interruptions and
voltage variations on
power supply input
lines.
IEC 61000-4-11
0% 0.5 cycle
At 0˚, 45˚, 90˚, 135˚,
180˚, 225˚, 270˚,
and 315˚
0% 1 cycle
And
70% 25/30 cycles
Singel phase: at 0
0% 300 cycle
N/A
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
N/A
Radiated RF
IEC 61000-4-3
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 U
T
is the a.c. mians voltage prior to application of the test level.
Table 3
Guidance and manufacturer’s declaration - electromagnetic Immunity
Radiated RF
IEC61000-4-3
(Test
specifications
for ENCLOSURE
PORT IMMUNITY
to RF wireless
communications
equipment)
Test
Frequency
(MHz)
Band
(MHz)
Service
Modulation
Modulation
(W)
Distance
(m)
IMMUNITY
TEST LEVEL
(V/m)
385
380–
390
TETRA
400
Pulse
modulation
18 Hz
1,8
0.3
27
450
380–
390
GMRS
460,
FRS
460
FM
± 5 kHz
deviation
1kHz 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
1700–
1990
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
2400–
2570
Bluetooth,
WLAN,
802.11
b/g/n,
RFID
2450,
LTE
Band 7
Pulse
modulation
217 Hz
2
0.3
28
5240
5100–
5800
WLAN
802.11
a/n
Pulse
modulation
217 Hz
0,2
0.3
9
5240
5785
6
7
8
9
10
Version: 1.0
Date modified: 2020-04-17
AD-102620.1
