Rossmax SB100 User manual

Cleaning and disinfection
Troubleshooting
Specification
1. Please clean the surface of the device before us-
ing. Wipe the device with medical alcohol (70%
isopropyl alcohol)first, and then let it dry in air or
clean it by dry clean fabric. When cleaning the de-
vice with water, the water temperature should be
lower than 60ºC
2. Using the medical alcohol to disinfect the prod-
uct after use, prevent from cross infection for next
time use.
3. The best storage environment of the device is -
20ºC to 70ºC ambient temperature and not higher
than 95% relative humidity.
4. Users are advised to calibrate the device termly (or
according to the calibrating program of hospital).
It also can be performed at the state-appointed
agent or just contact us for calibration.
Note: 1. Do not sterilize, autoclave or immerse this
device in liquid. Do not pour or spray any
liquids onto the device.
2. Do not use caustic or abrasive cleaning
agents, or any cleaning agent containing
ammonium chloride or isopropyl alcohol.
Symptoms Check points Corrections
SpO2 or
pulse rate
cannot
displayed
Applied nger
improperly.
Place the nger prop-
erly and try again.
SpO2 is too low to
detect
Try again; go to con-
sult with your physi-
cian if you are sure the
device works well.
SpO2 or
pulse rate are
not displayed
stably
Applied nger
improperly.
Place the nger prop-
erly and try again.
Finger is shaking
or body is moving. keep body steady
No display
when button
is pressed
Batteries run
down
Replace with new
batteries
Batteries not
inserted correctly. Re-insert batteries
The display
disappears
suddenly
The device will
auto power o
when it gets no
signal.
Normal
Low battery Replace with new
batteries
Note: If the unit does not work, return it to your
dealer. Under no circumstance should
you disassemble and repair the unit by
yourself.
SpO2
Measuring range 35%~99%, (the resolution is 1%).
Accuracy 70%~99%: ±2%, Below 35~69%:
unspecied.
Optical Sensor Red light (wavelength is 660nm),
Infrared (wavelength is 905/880nm)
Pulse
Measuring range 30bpm~250bpm (the resolution is 1
bpm)
Accuracy ±3bpm
Power source AAA × 2 (Alkaline)
Battery life Continually for 16 hours with two
alkaline batteries
Operating
Condition
Temperature: 5ºC~40ºC (41ºF ~ 104ºF),
Relative Humidity: 15-95% (non
condensing), Atmospheric pressure:
700hPa ~ 1013hkPa, Attitude: -1,280 to
12,000 feet (-390m to 3,658m)
Storage
Condition
Temperature: -25ºC~+70ºC(-13ºF ~
158ºF), Relative humidity: 15-90%(non
condensing), Atmospheric pressure:
700hPa ~ 1013hkPa, Attitude: -1,280 to
12,000 feet (-390m to 3,658m),
The time from 70ºC or -25ºC back to
use : 3 hours
Dimensions 63.5(L) × 34W) × 35(H) mm
Weight About 37g (without the batteries)
Standards IEC60601-1-2, Class B, IEC60601-1, Type
BF, ISO80601-2-61, MDD 93/42/EEC
Type BF applied parts
IP Classication IP22: Protection against harmful
ingress of water and particulate matter
Report No.: 17-02-RBO-033
cluding children) with restricted physical, sensory
or mental skills or a lack of experience and/or a lack
of knowledge, unless they are supervised by a per-
son who has responsibility for their safety or they
receive instructions from this person on how to use
the device. Children should be supervised around
the device to ensure they do not play with it.
- Neither of the displays for the pulse wave and pulse
bar allows the strength of the pulse or circulation to
be evaluated at the measurement site. Rather, they
are exclusively used to display the current signal
variation at the measurement site and do not en-
able reliable diagnostics for the pulse.
- A warning that other cables and accessories may
negatively aect EMC performance.
- A warning regarding stacking and location close to
other equipment.
- A warning that use of other accessories results in
non-compliance.
- The maximum temperature might reach 41.9°C
when operating for long time.
- The safety way for all people use is measuring for
10minutes, and turn it o for 20 minustes before
measure again.
Model: SB100
www.rossmax.com
Fingertip Pulse Oximeter
IN0SB100000000211 RI_IB_SB100_EN_TP_ver1803
Warranty Card
This instrument is covered by a 1 year guarantee from the date of purchase, batteries
and accessories are not included.The guarantee is valid only on presentation of the
guarantee card completed by the dealer confirming date of purchase or the receipt.
Opening or altering the instrument invalidates the guarantee. The guarantee does
not cover damage, accidents or non-compliance with the instruction manual. Please
contact your local seller/dealer or www.rossmax.com.
Customer Name: __________________________________
Address: _______________________________________
Telephone: _____________________________________
E-mail address: ___________________________________
Product Information: ______________________________
Date of purchase: _________________________________
Store where purchased:
______________________________________________
Rossmax InnoTek Corp.
12F., No. 189, Kang Chien Rd.,Taipei, 114,Taiwan.
CMC Medical Devices & Drugs S.L.
C/ Horacio Lengo Nº 18, CP 29006, Málaga, Spain
WARNING: The symbol on this product means that it's an electronic product
and following the European directive 2012/19/EU the electronic products have
to be dispose on your local recycling centre for safe treatment.
EMC guidance and manufacturer’s declaration
Recommended separation distances between portable and mobile RF communications equipment and the ME equipment
The Finger-tip pulse oximeter is intended for use in an electromagnetic environment in which radiated RF disturbances are con-
trolled.The customer or the user of the Finger-tip pulse oximeter can help prevent electromagnetic interference by maintaining a
minimum distance between portable and mobile RF communications equipment (transmitters) and the Finger-tip pulse oximeter
as recommended below, according to 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=[3.5/
V1]√P 80 MHz to 800 MHz , d=[3.5/ E1]√P 800 MHz to 2,5 GHz , d=[7/ E1]√P
0.01 0.1 0.1 0.2
0.1 0.4 0.4 0.7
11.2 1.2 2.3
10 3.7 3.7 7.4
100 11.7 11.7 23.3
Declaration – electromagnetic emissions
The Finger-tip pulse oximeter is intended for use in the electromagnetic environment specied below.The customer or the user of
the Finger-tip pulse oximeter should assure that it is used in such an environment.
Emissions test Compliance Electromagnetic environment - guidance
RF emissions CISPR 11 Group 1 Portable and mobile RF communications equipment should be used no
closer to any part of the EQUIPMENT or SYSTEM including cables, than the
recommended separation distance calculated from the equation applicable
to the frequency of the transmitter. Interference may occur in the vicinity of
equipment marked with the following symbol.
RF emissions CISPR 11 Class B The Finger-tip pulse oximeter 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 N/A
Voltage uctuations/Flicker emissions
IEC 61000-3-3 N/A
Declaration – electromagnetic emissions and immunity – for EQUIPMENT and SYSTEMS that are use in the professional health-
care facility environment or in the home healthcare environment
The Finger-tip pulse oximeter declaration – electromagnetic immunity
The Finger-tip pulse oximeter system is intended for use in the electromagnetic environment specied below.The customer or
the user of the Finger-tip pulse oximeter system should assure that it is used in such an environment.
Immunity test IEC 60601 test level Compliance level Electromagnetic environment - guidance
Conducted RF IEC
61000-4-6 3Vrms ; 6 Vrms ; 150 kHz to 80 MHz N/A Portable and mobile RF communications equipment should be used no closer to any part of the EQUIPMENT
or SYSTEM including cables, than the recommended
separation distance calculated from the equation ap-
plicable to the frequency of the transmitter. Interference
may occur in the vicinity of equipment marked with the
following symbol.
Radiated RF IEC
61000-4-3 3V/m ; 10V/m ; 80 MHz – 2.7 GHz l 80% 3V/m ; 10V/m ; 80 MHz – 2.7 GHz ; 80%
Proximity elds
from RF wireless
Communications
equipment IEC
61000-4-3
27V/m 385 MHz 27V/m 385 MHz
28V/m 450 MHz 28V/m 450 MHz
9V/m 710 MHz 9V/m 710 MHz
745 MHz 745 MHz
780 MHz 780 MHz
28V/m 810 MHz 28V/m 810 MHz
870 MHz 870 MHz
930 MHz 930 MHz
28V/m 1720 MHz 28 V/m 1720 MHz
1845 MHz 1845 MHz
1970 MHz 1970 MHz
28V/m 2450 MHz 28 V/m 2450 MHz
9V/m 5240 MHz 9 V/m 5240 MHz
5500 MHz 5500 MHz
5785 MHz 5785 MHz
Declaration – electromagnetic immunity
The Finger-tip pulse oximeter system is intended for use in the electromagnetic environment specied below.The customer or
the user of the Finger-tip pulse oximeter system should assure that it is used in such an environment.
Immunity test IEC 60601 test level Compliance level Electromagnetic environment - guidance
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
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 IEC 61000-4-4 ±2 kV for power supply lines ±1 kV for input/output lines N/A Mains power quality should be that of a typical commercial or hospital environment.
Surge IEC 61000-4-5 ±0.5 kV
±1 kV dierential mode
±2 kV common mode
N/A 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 IEC
61000-4-11
0 % UT; 0, 5 cycle At 0°, 45°,
90°, 135°, 180°, 225°, 270°
and 315°
0 % UT; 1 cycle And 70
% UT; 25/30 cycle Single
phase: at 0°
N/A Mains power quality should be that of a typical
commercial or hospital environment. If the user
of the EQUIPMENT or SYSTEM requires continued
operation during power mains interruptions, it is
recommended that the EQUIPMENT or SYSTEM
be powered from an uninterruptible power sup-
ply or a battery.
Power frequency (50/60
Hz) magnetic eld IEC
61000-4-8
30 A/m 30 A/m Power frequency magnetic elds should be at
levels characteristic of a typical location in a typi-
cal commercial or hospital environment.

Introduction
Error code for your reference
Rossmax Fingertip Pulse Oximeter SB100 is used
to measure arterial oxygen saturation (% SpO2) of
hemoglobin and pulse rate, an important indicator
of your respiratory function. It is non-invasive device
intended for spot-check of adult and pediatric
whose age is over 3 at home, hospital.
Attention: Consult the accompanying
documents. Please read this manual carefully
before use. Please be sure to keep this manual.
SENSOR ERROR:
Sensor cannot be detected,
return the device to your
local distributor or service
centre.
MEASURE ERROR:
Signals cannot be detect-
ed, turn the device off and
measure again.
Installing Batteries
1. Use thumb to slide battery
cover out
2. Insert or replace 2 “AAA” sized
batteries down with the
correct electrical polarity.
You need to replace the
batteries when
1. Battery icon is blinking on
display.
2. The function button is
pressed and nothing appears
on display.
Caution: Batteries may leak or explode if used or
disposed of improperly. Remove batteries
if the device will be stored for long time.
Do not use different types or brands of
batteries at the same time. Do not mix fully
charged and partially charged batteries at
the same time.
Attaching the lanyard
1. Insert the narrow end of
the lanyard through the
holder.
2. Draw the other end of the
lanyard through the loop
at the narrow end and
tighten.
How to use
1. Open the clip; press the Power On button as .
2. Information of software version appears; insert one
finger, nail side up, into the finger opening of the
pulse oximeter.
Note: if no finger insert, the device will auto shut off
after 8 seconds.
3. The pulse strength indication shows “ ”, pulse
oximeter begins its measurement as .
Note: make sure the finger is lying flat, Do not shake
and keep body steady during measurement as
.
4. Your SpO2 and pulse rate values will appear on the
screen after few seconds as .
Note: 1. Don’t remove your finger until the
measurement is completed.
2. If SpO2 and pulse rate cannot be detected, “
“ will appear on the screen as .
3. While pulse strength is low, the reading will
flicker.
Note:
1. The SpO2 sensor and photoelectric receiving tube
should be arranged in a way with the subject’s
arteriole in a position there between.
2. Make sure the optical path is free from any optical
obstacles like rubberized fabric.
3. Excessive ambient light may affect the measuring
result. It includes fluorescent lamp, dual ruby light,
infrared heater, direct sunlight and etc.
4. Strenuous action of the subject or extreme
electrosurgical interference may also affect the
accuracy.
Cautionary Notes
- This device is to be operated by trained personnel
only.
- This device has no audible and it intended only for
spot-checking, but not medical result evaluation.
- This device is designed to determine the percent-
age of arterial oxygen saturation of functional he-
moglobin. Factors that may degrade pulse oximeter
performance or aect the accuracy of the measure-
ment include the following:
• Do not apply the pulse oximeter on the same arm
as a blood pressure cu, arterial catheter or infusion
line(s)
• Excessive light, such as sunlight or direct home
lighting.
• Not steady at the site of application (e.g. trem-
bling)
• Moisture in the device
• Improperly applied device
• Finger is too large or too small to t into the device.
• Poor pulse quality
• Venous pulsations
• Anemia or low hemoglobin concentrations.
• Cardiogreen and other intravascular dyes
• Carboxyhemoglobin
• Methemoglobin
• Dysfunctional hemoglobin
• Articial nails or ngernail polish
• On ngers with anatomical changes, oedemas,
scars or burns.
- Using the device for long periods may cause pain
for people with circulatory disorders. Reposition
the device at least once every 4 hours to allow the
patient’s skin to breath and to check patient’s con-
dition regularly.
- Do not use the device near ammable or explosive
gas mixtures.
- Do not use the device during an MRI or CT scan, be
used no closer than 30 cm (12 inches) to any part
of the [ME EQUIPMENT or ME SYSTEM], including
cables specied by the manufacturer
- The device may not work when circulation is re-
duced. Warm or rub the nger, or re-position the
device.
- This device is a precision electronic instrument and
must be repaired by qualied technical profession-
als. Field repair of the device is not possible. Do no
attempt to open the case or repair the electronics.
Opening the case may damage the device and
void the warranty.
- Do not overextend the device’s spring.
- A functional tester cannot be used to access the
accuracy of a pulse oximeter monitor.
- Do not self-diagnose or self-medicate on the ba-
sis of the measurements without consulting your
doctor. In particular, do not start taking any new
medication or change the type and/or dosage of
any existing medication without prior approval.
- Do not look directly inside the housing during the
measurement. The red light and the invisible infra-
red light in the pulse oximeter are harmful to your
eyes.
- This device is not intended for use by people (in-
1. SpO2 icon
2. Pulse strength
indication
3. Pulse rate icon
7
1
2
3
4
5
6
4. Beats per minute
5. Power On Button
6. Battery icon
7. Battery compartment
Name/ Functions of each part

Introduction
Error code for your reference
Rossmax Fingertip Pulse Oximeter SB100 is used
to measure arterial oxygen saturation (% SpO2) of
hemoglobin and pulse rate, an important indicator
of your respiratory function. It is non-invasive device
intended for spot-check of adult and pediatric
whose age is over 3 at home, hospital.
Attention: Consult the accompanying
documents. Please read this manual carefully
before use. Please be sure to keep this manual.
SENSOR ERROR:
Sensor cannot be detected,
return the device to your
local distributor or service
centre.
MEASURE ERROR:
Signals cannot be detect-
ed, turn the device off and
measure again.
Installing Batteries
1. Use thumb to slide battery
cover out
2. Insert or replace 2 “AAA” sized
batteries down with the
correct electrical polarity.
You need to replace the
batteries when
1. Battery icon is blinking on
display.
2. The function button is
pressed and nothing appears
on display.
Caution: Batteries may leak or explode if used or
disposed of improperly. Remove batteries
if the device will be stored for long time.
Do not use different types or brands of
batteries at the same time. Do not mix fully
charged and partially charged batteries at
the same time.
Attaching the lanyard
1. Insert the narrow end of
the lanyard through the
holder.
2. Draw the other end of the
lanyard through the loop
at the narrow end and
tighten.
How to use
1. Open the clip; press the Power On button as .
2. Information of software version appears; insert one
finger, nail side up, into the finger opening of the
pulse oximeter.
Note: if no finger insert, the device will auto shut off
after 8 seconds.
3. The pulse strength indication shows “ ”, pulse
oximeter begins its measurement as .
Note: make sure the finger is lying flat, Do not shake
and keep body steady during measurement as
.
4. Your SpO2 and pulse rate values will appear on the
screen after few seconds as .
Note: 1. Don’t remove your finger until the
measurement is completed.
2. If SpO2 and pulse rate cannot be detected, “
“ will appear on the screen as .
3. While pulse strength is low, the reading will
flicker.
Note:
1. The SpO2 sensor and photoelectric receiving tube
should be arranged in a way with the subject’s
arteriole in a position there between.
2. Make sure the optical path is free from any optical
obstacles like rubberized fabric.
3. Excessive ambient light may affect the measuring
result. It includes fluorescent lamp, dual ruby light,
infrared heater, direct sunlight and etc.
4. Strenuous action of the subject or extreme
electrosurgical interference may also affect the
accuracy.
Cautionary Notes
- This device is to be operated by trained personnel
only.
- This device has no audible and it intended only for
spot-checking, but not medical result evaluation.
- This device is designed to determine the percent-
age of arterial oxygen saturation of functional he-
moglobin. Factors that may degrade pulse oximeter
performance or aect the accuracy of the measure-
ment include the following:
• Do not apply the pulse oximeter on the same arm
as a blood pressure cu, arterial catheter or infusion
line(s)
• Excessive light, such as sunlight or direct home
lighting.
• Not steady at the site of application (e.g. trem-
bling)
• Moisture in the device
• Improperly applied device
• Finger is too large or too small to t into the device.
• Poor pulse quality
• Venous pulsations
• Anemia or low hemoglobin concentrations.
• Cardiogreen and other intravascular dyes
• Carboxyhemoglobin
• Methemoglobin
• Dysfunctional hemoglobin
• Articial nails or ngernail polish
• On ngers with anatomical changes, oedemas,
scars or burns.
- Using the device for long periods may cause pain
for people with circulatory disorders. Reposition
the device at least once every 4 hours to allow the
patient’s skin to breath and to check patient’s con-
dition regularly.
- Do not use the device near ammable or explosive
gas mixtures.
- Do not use the device during an MRI or CT scan, be
used no closer than 30 cm (12 inches) to any part
of the [ME EQUIPMENT or ME SYSTEM], including
cables specied by the manufacturer
- The device may not work when circulation is re-
duced. Warm or rub the nger, or re-position the
device.
- This device is a precision electronic instrument and
must be repaired by qualied technical profession-
als. Field repair of the device is not possible. Do no
attempt to open the case or repair the electronics.
Opening the case may damage the device and
void the warranty.
- Do not overextend the device’s spring.
- A functional tester cannot be used to access the
accuracy of a pulse oximeter monitor.
- Do not self-diagnose or self-medicate on the ba-
sis of the measurements without consulting your
doctor. In particular, do not start taking any new
medication or change the type and/or dosage of
any existing medication without prior approval.
- Do not look directly inside the housing during the
measurement. The red light and the invisible infra-
red light in the pulse oximeter are harmful to your
eyes.
- This device is not intended for use by people (in-
1. SpO2 icon
2. Pulse strength
indication
3. Pulse rate icon
7
1
2
3
4
5
6
4. Beats per minute
5. Power On Button
6. Battery icon
7. Battery compartment
Name/ Functions of each part

Introduction
Error code for your reference
Rossmax Fingertip Pulse Oximeter SB100 is used
to measure arterial oxygen saturation (% SpO2) of
hemoglobin and pulse rate, an important indicator
of your respiratory function. It is non-invasive device
intended for spot-check of adult and pediatric
whose age is over 3 at home, hospital.
Attention: Consult the accompanying
documents. Please read this manual carefully
before use. Please be sure to keep this manual.
SENSOR ERROR:
Sensor cannot be detected,
return the device to your
local distributor or service
centre.
MEASURE ERROR:
Signals cannot be detect-
ed, turn the device off and
measure again.
Installing Batteries
1. Use thumb to slide battery
cover out
2. Insert or replace 2 “AAA” sized
batteries down with the
correct electrical polarity.
You need to replace the
batteries when
1. Battery icon is blinking on
display.
2. The function button is
pressed and nothing appears
on display.
Caution: Batteries may leak or explode if used or
disposed of improperly. Remove batteries
if the device will be stored for long time.
Do not use different types or brands of
batteries at the same time. Do not mix fully
charged and partially charged batteries at
the same time.
Attaching the lanyard
1. Insert the narrow end of
the lanyard through the
holder.
2. Draw the other end of the
lanyard through the loop
at the narrow end and
tighten.
How to use
1. Open the clip; press the Power On button as .
2. Information of software version appears; insert one
finger, nail side up, into the finger opening of the
pulse oximeter.
Note: if no finger insert, the device will auto shut off
after 8 seconds.
3. The pulse strength indication shows “ ”, pulse
oximeter begins its measurement as .
Note: make sure the finger is lying flat, Do not shake
and keep body steady during measurement as
.
4. Your SpO2 and pulse rate values will appear on the
screen after few seconds as .
Note: 1. Don’t remove your finger until the
measurement is completed.
2. If SpO2 and pulse rate cannot be detected, “
“ will appear on the screen as .
3. While pulse strength is low, the reading will
flicker.
Note:
1. The SpO2 sensor and photoelectric receiving tube
should be arranged in a way with the subject’s
arteriole in a position there between.
2. Make sure the optical path is free from any optical
obstacles like rubberized fabric.
3. Excessive ambient light may affect the measuring
result. It includes fluorescent lamp, dual ruby light,
infrared heater, direct sunlight and etc.
4. Strenuous action of the subject or extreme
electrosurgical interference may also affect the
accuracy.
Cautionary Notes
- This device is to be operated by trained personnel
only.
- This device has no audible and it intended only for
spot-checking, but not medical result evaluation.
- This device is designed to determine the percent-
age of arterial oxygen saturation of functional he-
moglobin. Factors that may degrade pulse oximeter
performance or aect the accuracy of the measure-
ment include the following:
• Do not apply the pulse oximeter on the same arm
as a blood pressure cu, arterial catheter or infusion
line(s)
• Excessive light, such as sunlight or direct home
lighting.
• Not steady at the site of application (e.g. trem-
bling)
• Moisture in the device
• Improperly applied device
• Finger is too large or too small to t into the device.
• Poor pulse quality
• Venous pulsations
• Anemia or low hemoglobin concentrations.
• Cardiogreen and other intravascular dyes
• Carboxyhemoglobin
• Methemoglobin
• Dysfunctional hemoglobin
• Articial nails or ngernail polish
• On ngers with anatomical changes, oedemas,
scars or burns.
- Using the device for long periods may cause pain
for people with circulatory disorders. Reposition
the device at least once every 4 hours to allow the
patient’s skin to breath and to check patient’s con-
dition regularly.
- Do not use the device near ammable or explosive
gas mixtures.
- Do not use the device during an MRI or CT scan, be
used no closer than 30 cm (12 inches) to any part
of the [ME EQUIPMENT or ME SYSTEM], including
cables specied by the manufacturer
- The device may not work when circulation is re-
duced. Warm or rub the nger, or re-position the
device.
- This device is a precision electronic instrument and
must be repaired by qualied technical profession-
als. Field repair of the device is not possible. Do no
attempt to open the case or repair the electronics.
Opening the case may damage the device and
void the warranty.
- Do not overextend the device’s spring.
- A functional tester cannot be used to access the
accuracy of a pulse oximeter monitor.
- Do not self-diagnose or self-medicate on the ba-
sis of the measurements without consulting your
doctor. In particular, do not start taking any new
medication or change the type and/or dosage of
any existing medication without prior approval.
- Do not look directly inside the housing during the
measurement. The red light and the invisible infra-
red light in the pulse oximeter are harmful to your
eyes.
- This device is not intended for use by people (in-
1. SpO2 icon
2. Pulse strength
indication
3. Pulse rate icon
7
1
2
3
4
5
6
4. Beats per minute
5. Power On Button
6. Battery icon
7. Battery compartment
Name/ Functions of each part

Introduction
Error code for your reference
Rossmax Fingertip Pulse Oximeter SB100 is used
to measure arterial oxygen saturation (% SpO2) of
hemoglobin and pulse rate, an important indicator
of your respiratory function. It is non-invasive device
intended for spot-check of adult and pediatric
whose age is over 3 at home, hospital.
Attention: Consult the accompanying
documents. Please read this manual carefully
before use. Please be sure to keep this manual.
SENSOR ERROR:
Sensor cannot be detected,
return the device to your
local distributor or service
centre.
MEASURE ERROR:
Signals cannot be detect-
ed, turn the device off and
measure again.
Installing Batteries
1. Use thumb to slide battery
cover out
2. Insert or replace 2 “AAA” sized
batteries down with the
correct electrical polarity.
You need to replace the
batteries when
1. Battery icon is blinking on
display.
2. The function button is
pressed and nothing appears
on display.
Caution: Batteries may leak or explode if used or
disposed of improperly. Remove batteries
if the device will be stored for long time.
Do not use different types or brands of
batteries at the same time. Do not mix fully
charged and partially charged batteries at
the same time.
Attaching the lanyard
1. Insert the narrow end of
the lanyard through the
holder.
2. Draw the other end of the
lanyard through the loop
at the narrow end and
tighten.
How to use
1. Open the clip; press the Power On button as .
2. Information of software version appears; insert one
finger, nail side up, into the finger opening of the
pulse oximeter.
Note: if no finger insert, the device will auto shut off
after 8 seconds.
3. The pulse strength indication shows “ ”, pulse
oximeter begins its measurement as .
Note: make sure the finger is lying flat, Do not shake
and keep body steady during measurement as
.
4. Your SpO2 and pulse rate values will appear on the
screen after few seconds as .
Note: 1. Don’t remove your finger until the
measurement is completed.
2. If SpO2 and pulse rate cannot be detected, “
“ will appear on the screen as .
3. While pulse strength is low, the reading will
flicker.
Note:
1. The SpO2 sensor and photoelectric receiving tube
should be arranged in a way with the subject’s
arteriole in a position there between.
2. Make sure the optical path is free from any optical
obstacles like rubberized fabric.
3. Excessive ambient light may affect the measuring
result. It includes fluorescent lamp, dual ruby light,
infrared heater, direct sunlight and etc.
4. Strenuous action of the subject or extreme
electrosurgical interference may also affect the
accuracy.
Cautionary Notes
- This device is to be operated by trained personnel
only.
- This device has no audible and it intended only for
spot-checking, but not medical result evaluation.
- This device is designed to determine the percent-
age of arterial oxygen saturation of functional he-
moglobin. Factors that may degrade pulse oximeter
performance or aect the accuracy of the measure-
ment include the following:
• Do not apply the pulse oximeter on the same arm
as a blood pressure cu, arterial catheter or infusion
line(s)
• Excessive light, such as sunlight or direct home
lighting.
• Not steady at the site of application (e.g. trem-
bling)
• Moisture in the device
• Improperly applied device
• Finger is too large or too small to t into the device.
• Poor pulse quality
• Venous pulsations
• Anemia or low hemoglobin concentrations.
• Cardiogreen and other intravascular dyes
• Carboxyhemoglobin
• Methemoglobin
• Dysfunctional hemoglobin
• Articial nails or ngernail polish
• On ngers with anatomical changes, oedemas,
scars or burns.
- Using the device for long periods may cause pain
for people with circulatory disorders. Reposition
the device at least once every 4 hours to allow the
patient’s skin to breath and to check patient’s con-
dition regularly.
- Do not use the device near ammable or explosive
gas mixtures.
- Do not use the device during an MRI or CT scan, be
used no closer than 30 cm (12 inches) to any part
of the [ME EQUIPMENT or ME SYSTEM], including
cables specied by the manufacturer
- The device may not work when circulation is re-
duced. Warm or rub the nger, or re-position the
device.
- This device is a precision electronic instrument and
must be repaired by qualied technical profession-
als. Field repair of the device is not possible. Do no
attempt to open the case or repair the electronics.
Opening the case may damage the device and
void the warranty.
- Do not overextend the device’s spring.
- A functional tester cannot be used to access the
accuracy of a pulse oximeter monitor.
- Do not self-diagnose or self-medicate on the ba-
sis of the measurements without consulting your
doctor. In particular, do not start taking any new
medication or change the type and/or dosage of
any existing medication without prior approval.
- Do not look directly inside the housing during the
measurement. The red light and the invisible infra-
red light in the pulse oximeter are harmful to your
eyes.
- This device is not intended for use by people (in-
1. SpO2 icon
2. Pulse strength
indication
3. Pulse rate icon
7
1
2
3
4
5
6
4. Beats per minute
5. Power On Button
6. Battery icon
7. Battery compartment
Name/ Functions of each part

Cleaning and disinfection
Troubleshooting
Specification
1. Please clean the surface of the device before us-
ing. Wipe the device with medical alcohol (70%
isopropyl alcohol)first, and then let it dry in air or
clean it by dry clean fabric. When cleaning the de-
vice with water, the water temperature should be
lower than 60ºC
2. Using the medical alcohol to disinfect the prod-
uct after use, prevent from cross infection for next
time use.
3. The best storage environment of the device is -
20ºC to 70ºC ambient temperature and not higher
than 95% relative humidity.
4. Users are advised to calibrate the device termly (or
according to the calibrating program of hospital).
It also can be performed at the state-appointed
agent or just contact us for calibration.
Note: 1. Do not sterilize, autoclave or immerse this
device in liquid. Do not pour or spray any
liquids onto the device.
2. Do not use caustic or abrasive cleaning
agents, or any cleaning agent containing
ammonium chloride or isopropyl alcohol.
Symptoms Check points Corrections
SpO2 or
pulse rate
cannot
displayed
Applied nger
improperly.
Place the nger prop-
erly and try again.
SpO2 is too low to
detect
Try again; go to con-
sult with your physi-
cian if you are sure the
device works well.
SpO2 or
pulse rate are
not displayed
stably
Applied nger
improperly.
Place the nger prop-
erly and try again.
Finger is shaking
or body is moving. keep body steady
No display
when button
is pressed
Batteries run
down
Replace with new
batteries
Batteries not
inserted correctly. Re-insert batteries
The display
disappears
suddenly
The device will
auto power o
when it gets no
signal.
Normal
Low battery Replace with new
batteries
Note: If the unit does not work, return it to your
dealer. Under no circumstance should
you disassemble and repair the unit by
yourself.
SpO2
Measuring range 35%~99%, (the resolution is 1%).
Accuracy 70%~99%: ±2%, Below 35~69%:
unspecied.
Optical Sensor Red light (wavelength is 660nm),
Infrared (wavelength is 905/880nm)
Pulse
Measuring range 30bpm~250bpm (the resolution is 1
bpm)
Accuracy ±3bpm
Power source AAA × 2 (Alkaline)
Battery life Continually for 16 hours with two
alkaline batteries
Operating
Condition
Temperature: 5ºC~40ºC (41ºF ~ 104ºF),
Relative Humidity: 15-95% (non
condensing), Atmospheric pressure:
700hPa ~ 1013hkPa, Attitude: -1,280 to
12,000 feet (-390m to 3,658m)
Storage
Condition
Temperature: -25ºC~+70ºC(-13ºF ~
158ºF), Relative humidity: 15-90%(non
condensing), Atmospheric pressure:
700hPa ~ 1013hkPa, Attitude: -1,280 to
12,000 feet (-390m to 3,658m),
The time from 70ºC or -25ºC back to
use : 3 hours
Dimensions 63.5(L) × 34W) × 35(H) mm
Weight About 37g (without the batteries)
Standards IEC60601-1-2, Class B, IEC60601-1, Type
BF, ISO80601-2-61, MDD 93/42/EEC
Type BF applied parts
IP Classication IP22: Protection against harmful
ingress of water and particulate matter
Report No.: 17-02-RBO-033
cluding children) with restricted physical, sensory
or mental skills or a lack of experience and/or a lack
of knowledge, unless they are supervised by a per-
son who has responsibility for their safety or they
receive instructions from this person on how to use
the device. Children should be supervised around
the device to ensure they do not play with it.
- Neither of the displays for the pulse wave and pulse
bar allows the strength of the pulse or circulation to
be evaluated at the measurement site. Rather, they
are exclusively used to display the current signal
variation at the measurement site and do not en-
able reliable diagnostics for the pulse.
- A warning that other cables and accessories may
negatively aect EMC performance.
- A warning regarding stacking and location close to
other equipment.
- A warning that use of other accessories results in
non-compliance.
- The maximum temperature might reach 41.9°C
when operating for long time.
- The safety way for all people use is measuring for
10minutes, and turn it o for 20 minustes before
measure again.
Model: SB100
www.rossmax.com
Fingertip Pulse Oximeter
IN0SB100000000211 RI_IB_SB100_EN_TP_ver1803
Warranty Card
This instrument is covered by a 1 year guarantee from the date of purchase, batteries
and accessories are not included.The guarantee is valid only on presentation of the
guarantee card completed by the dealer confirming date of purchase or the receipt.
Opening or altering the instrument invalidates the guarantee. The guarantee does
not cover damage, accidents or non-compliance with the instruction manual. Please
contact your local seller/dealer or www.rossmax.com.
Customer Name: __________________________________
Address: _______________________________________
Telephone: _____________________________________
E-mail address: ___________________________________
Product Information: ______________________________
Date of purchase: _________________________________
Store where purchased:
______________________________________________
Rossmax InnoTek Corp.
12F., No. 189, Kang Chien Rd.,Taipei, 114,Taiwan.
CMC Medical Devices & Drugs S.L.
C/ Horacio Lengo Nº 18, CP 29006, Málaga, Spain
WARNING: The symbol on this product means that it's an electronic product
and following the European directive 2012/19/EU the electronic products have
to be dispose on your local recycling centre for safe treatment.
EMC guidance and manufacturer’s declaration
Recommended separation distances between portable and mobile RF communications equipment and the ME equipment
The Finger-tip pulse oximeter is intended for use in an electromagnetic environment in which radiated RF disturbances are con-
trolled.The customer or the user of the Finger-tip pulse oximeter can help prevent electromagnetic interference by maintaining a
minimum distance between portable and mobile RF communications equipment (transmitters) and the Finger-tip pulse oximeter
as recommended below, according to 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=[3.5/
V1]√P 80 MHz to 800 MHz , d=[3.5/ E1]√P 800 MHz to 2,5 GHz , d=[7/ E1]√P
0.01 0.1 0.1 0.2
0.1 0.4 0.4 0.7
11.2 1.2 2.3
10 3.7 3.7 7.4
100 11.7 11.7 23.3
Declaration – electromagnetic emissions
The Finger-tip pulse oximeter is intended for use in the electromagnetic environment specied below.The customer or the user of
the Finger-tip pulse oximeter should assure that it is used in such an environment.
Emissions test Compliance Electromagnetic environment - guidance
RF emissions CISPR 11 Group 1 Portable and mobile RF communications equipment should be used no
closer to any part of the EQUIPMENT or SYSTEM including cables, than the
recommended separation distance calculated from the equation applicable
to the frequency of the transmitter. Interference may occur in the vicinity of
equipment marked with the following symbol.
RF emissions CISPR 11 Class B The Finger-tip pulse oximeter 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 N/A
Voltage uctuations/Flicker emissions
IEC 61000-3-3 N/A
Declaration – electromagnetic emissions and immunity – for EQUIPMENT and SYSTEMS that are use in the professional health-
care facility environment or in the home healthcare environment
The Finger-tip pulse oximeter declaration – electromagnetic immunity
The Finger-tip pulse oximeter system is intended for use in the electromagnetic environment specied below.The customer or
the user of the Finger-tip pulse oximeter system should assure that it is used in such an environment.
Immunity test IEC 60601 test level Compliance level Electromagnetic environment - guidance
Conducted RF IEC
61000-4-6 3Vrms ; 6Vrms ; 150 kHz to 80 MHz N/A Portable and mobile RF communications equipment should be used no closer to any part of the EQUIPMENT
or SYSTEM including cables, than the recommended
separation distance calculated from the equation ap-
plicable to the frequency of the transmitter. Interference
may occur in the vicinity of equipment marked with the
following symbol.
Radiated RF IEC
61000-4-3 3V/m ; 10V/m ; 80 MHz – 2.7 GHz l 80% 3V/m ; 10V/m ; 80 MHz – 2.7 GHz ; 80%
Proximity elds
from RF wireless
Communications
equipment IEC
61000-4-3
27V/m 385 MHz 27V/m 385 MHz
28V/m 450 MHz 28V/m 450 MHz
9V/m 710 MHz 9V/m 710 MHz
745 MHz 745 MHz
780 MHz 780 MHz
28V/m 810 MHz 28V/m 810 MHz
870 MHz 870 MHz
930 MHz 930 MHz
28V/m 1720 MHz 28V/m 1720 MHz
1845 MHz 1845 MHz
1970 MHz 1970 MHz
28V/m 2450 MHz 28V/m 2450 MHz
9V/m 5240 MHz 9V/m 5240 MHz
5500 MHz 5500 MHz
5785 MHz 5785 MHz
Declaration – electromagnetic immunity
The Finger-tip pulse oximeter system is intended for use in the electromagnetic environment specied below.The customer or
the user of the Finger-tip pulse oximeter system should assure that it is used in such an environment.
Immunity test IEC 60601 test level Compliance level Electromagnetic environment - guidance
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
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 IEC 61000-4-4 ±2 kV for power supply lines ±1 kV for input/output lines N/A Mains power quality should be that of a typical commercial or hospital environment.
Surge IEC 61000-4-5 ±0.5 kV
±1 kV dierential mode
±2 kV common mode
N/A 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 IEC
61000-4-11
0 % UT; 0, 5 cycle At 0°, 45°,
90°, 135°, 180°, 225°, 270°
and 315°
0 % UT; 1 cycle And 70
% UT; 25/30 cycle Single
phase: at 0°
N/A Mains power quality should be that of a typical
commercial or hospital environment. If the user
of the EQUIPMENT or SYSTEM requires continued
operation during power mains interruptions, it is
recommended that the EQUIPMENT or SYSTEM
be powered from an uninterruptible power sup-
ply or a battery.
Power frequency (50/60
Hz) magnetic eld IEC
61000-4-8
30 A/m 30 A/m Power frequency magnetic elds should be at
levels characteristic of a typical location in a typi-
cal commercial or hospital environment.

Cleaning and disinfection
Troubleshooting
Specification
1. Please clean the surface of the device before us-
ing. Wipe the device with medical alcohol (70%
isopropyl alcohol)first, and then let it dry in air or
clean it by dry clean fabric. When cleaning the de-
vice with water, the water temperature should be
lower than 60ºC
2. Using the medical alcohol to disinfect the prod-
uct after use, prevent from cross infection for next
time use.
3. The best storage environment of the device is -
20ºC to 70ºC ambient temperature and not higher
than 95% relative humidity.
4. Users are advised to calibrate the device termly (or
according to the calibrating program of hospital).
It also can be performed at the state-appointed
agent or just contact us for calibration.
Note: 1. Do not sterilize, autoclave or immerse this
device in liquid. Do not pour or spray any
liquids onto the device.
2. Do not use caustic or abrasive cleaning
agents, or any cleaning agent containing
ammonium chloride or isopropyl alcohol.
Symptoms Check points Corrections
SpO2 or
pulse rate
cannot
displayed
Applied nger
improperly.
Place the nger prop-
erly and try again.
SpO2 is too low to
detect
Try again; go to con-
sult with your physi-
cian if you are sure the
device works well.
SpO2 or
pulse rate are
not displayed
stably
Applied nger
improperly.
Place the nger prop-
erly and try again.
Finger is shaking
or body is moving. keep body steady
No display
when button
is pressed
Batteries run
down
Replace with new
batteries
Batteries not
inserted correctly. Re-insert batteries
The display
disappears
suddenly
The device will
auto power o
when it gets no
signal.
Normal
Low battery Replace with new
batteries
Note: If the unit does not work, return it to your
dealer. Under no circumstance should
you disassemble and repair the unit by
yourself.
SpO2
Measuring range 35%~99%, (the resolution is 1%).
Accuracy 70%~99%: ±2%, Below 35~69%:
unspecied.
Optical Sensor Red light (wavelength is 660nm),
Infrared (wavelength is 905/880nm)
Pulse
Measuring range 30bpm~250bpm (the resolution is 1
bpm)
Accuracy ±3bpm
Power source AAA × 2 (Alkaline)
Battery life Continually for 16 hours with two
alkaline batteries
Operating
Condition
Temperature: 5ºC~40ºC (41ºF ~ 104ºF),
Relative Humidity: 15-95% (non
condensing), Atmospheric pressure:
700hPa ~ 1013hkPa, Attitude: -1,280 to
12,000 feet (-390m to 3,658m)
Storage
Condition
Temperature: -25ºC~+70ºC(-13ºF ~
158ºF), Relative humidity: 15-90%(non
condensing), Atmospheric pressure:
700hPa ~ 1013hkPa, Attitude: -1,280 to
12,000 feet (-390m to 3,658m),
The time from 70ºC or -25ºC back to
use : 3 hours
Dimensions 63.5(L) × 34W) × 35(H) mm
Weight About 37g (without the batteries)
Standards IEC60601-1-2, Class B, IEC60601-1, Type
BF, ISO80601-2-61, MDD 93/42/EEC
Type BF applied parts
IP Classication IP22: Protection against harmful
ingress of water and particulate matter
Report No.: 17-02-RBO-033
cluding children) with restricted physical, sensory
or mental skills or a lack of experience and/or a lack
of knowledge, unless they are supervised by a per-
son who has responsibility for their safety or they
receive instructions from this person on how to use
the device. Children should be supervised around
the device to ensure they do not play with it.
- Neither of the displays for the pulse wave and pulse
bar allows the strength of the pulse or circulation to
be evaluated at the measurement site. Rather, they
are exclusively used to display the current signal
variation at the measurement site and do not en-
able reliable diagnostics for the pulse.
- A warning that other cables and accessories may
negatively aect EMC performance.
- A warning regarding stacking and location close to
other equipment.
- A warning that use of other accessories results in
non-compliance.
- The maximum temperature might reach 41.9°C
when operating for long time.
- The safety way for all people use is measuring for
10minutes, and turn it o for 20 minustes before
measure again.
Model: SB100
www.rossmax.com
Fingertip Pulse Oximeter
IN0SB100000000211 RI_IB_SB100_EN_TP_ver1803
Warranty Card
This instrument is covered by a 1 year guarantee from the date of purchase, batteries
and accessories are not included.The guarantee is valid only on presentation of the
guarantee card completed by the dealer confirming date of purchase or the receipt.
Opening or altering the instrument invalidates the guarantee. The guarantee does
not cover damage, accidents or non-compliance with the instruction manual. Please
contact your local seller/dealer or www.rossmax.com.
Customer Name: __________________________________
Address: _______________________________________
Telephone: _____________________________________
E-mail address: ___________________________________
Product Information: ______________________________
Date of purchase: _________________________________
Store where purchased:
______________________________________________
Rossmax InnoTek Corp.
12F., No. 189, Kang Chien Rd.,Taipei, 114,Taiwan.
CMC Medical Devices & Drugs S.L.
C/ Horacio Lengo Nº 18, CP 29006, Málaga, Spain
WARNING: The symbol on this product means that it's an electronic product
and following the European directive 2012/19/EU the electronic products have
to be dispose on your local recycling centre for safe treatment.
EMC guidance and manufacturer’s declaration
Recommended separation distances between portable and mobile RF communications equipment and the ME equipment
The Finger-tip pulse oximeter is intended for use in an electromagnetic environment in which radiated RF disturbances are con-
trolled.The customer or the user of the Finger-tip pulse oximeter can help prevent electromagnetic interference by maintaining a
minimum distance between portable and mobile RF communications equipment (transmitters) and the Finger-tip pulse oximeter
as recommended below, according to 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=[3.5/
V1]√P 80 MHz to 800 MHz , d=[3.5/ E1]√P 800 MHz to 2,5 GHz , d=[7/ E1]√P
0.01 0.1 0.1 0.2
0.1 0.4 0.4 0.7
11.2 1.2 2.3
10 3.7 3.7 7.4
100 11.7 11.7 23.3
Declaration – electromagnetic emissions
The Finger-tip pulse oximeter is intended for use in the electromagnetic environment specied below.The customer or the user of
the Finger-tip pulse oximeter should assure that it is used in such an environment.
Emissions test Compliance Electromagnetic environment - guidance
RF emissions CISPR 11 Group 1 Portable and mobile RF communications equipment should be used no
closer to any part of the EQUIPMENT or SYSTEM including cables, than the
recommended separation distance calculated from the equation applicable
to the frequency of the transmitter. Interference may occur in the vicinity of
equipment marked with the following symbol.
RF emissions CISPR 11 Class B The Finger-tip pulse oximeter 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 N/A
Voltage uctuations/Flicker emissions
IEC 61000-3-3 N/A
Declaration – electromagnetic emissions and immunity – for EQUIPMENT and SYSTEMS that are use in the professional health-
care facility environment or in the home healthcare environment
The Finger-tip pulse oximeter declaration – electromagnetic immunity
The Finger-tip pulse oximeter system is intended for use in the electromagnetic environment specied below.The customer or
the user of the Finger-tip pulse oximeter system should assure that it is used in such an environment.
Immunity test IEC 60601 test level Compliance level Electromagnetic environment - guidance
Conducted RF IEC
61000-4-6 3 Vrms ; 6Vrms ; 150 kHz to 80 MHz N/A Portable and mobile RF communications equipment should be used no closer to any part of the EQUIPMENT
or SYSTEM including cables, than the recommended
separation distance calculated from the equation ap-
plicable to the frequency of the transmitter. Interference
may occur in the vicinity of equipment marked with the
following symbol.
Radiated RF IEC
61000-4-3 3 V/m ; 10V/m ; 80 MHz – 2.7 GHz l 80% 3 V/m ; 10V/m ; 80 MHz – 2.7 GHz ; 80%
Proximity elds
from RF wireless
Communications
equipment IEC
61000-4-3
27V/m 385 MHz 27 V/m 385 MHz
28V/m 450 MHz 28 V/m 450 MHz
9V/m 710 MHz 9 V/m 710 MHz
745 MHz 745 MHz
780 MHz 780 MHz
28V/m 810 MHz 28 V/m 810 MHz
870 MHz 870 MHz
930 MHz 930 MHz
28V/m 1720 MHz 28V/m 1720 MHz
1845 MHz 1845 MHz
1970 MHz 1970 MHz
28V/m 2450 MHz 28V/m 2450 MHz
9V/m 5240 MHz 9V/m 5240 MHz
5500 MHz 5500 MHz
5785 MHz 5785 MHz
Declaration – electromagnetic immunity
The Finger-tip pulse oximeter system is intended for use in the electromagnetic environment specied below.The customer or
the user of the Finger-tip pulse oximeter system should assure that it is used in such an environment.
Immunity test IEC 60601 test level Compliance level Electromagnetic environment - guidance
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
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 IEC 61000-4-4 ±2 kV for power supply lines ±1 kV for input/output lines N/A Mains power quality should be that of a typical commercial or hospital environment.
Surge IEC 61000-4-5 ±0.5 kV
±1 kV dierential mode
±2 kV common mode
N/A 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 IEC
61000-4-11
0 % UT; 0, 5 cycle At 0°, 45°,
90°, 135°, 180°, 225°, 270°
and 315°
0 % UT; 1 cycle And 70
% UT; 25/30 cycle Single
phase: at 0°
N/A Mains power quality should be that of a typical
commercial or hospital environment. If the user
of the EQUIPMENT or SYSTEM requires continued
operation during power mains interruptions, it is
recommended that the EQUIPMENT or SYSTEM
be powered from an uninterruptible power sup-
ply or a battery.
Power frequency (50/60
Hz) magnetic eld IEC
61000-4-8
30 A/m 30 A/m Power frequency magnetic elds should be at
levels characteristic of a typical location in a typi-
cal commercial or hospital environment.

Cleaning and disinfection
Troubleshooting
Specification
1. Please clean the surface of the device before us-
ing. Wipe the device with medical alcohol (70%
isopropyl alcohol)first, and then let it dry in air or
clean it by dry clean fabric. When cleaning the de-
vice with water, the water temperature should be
lower than 60ºC
2. Using the medical alcohol to disinfect the prod-
uct after use, prevent from cross infection for next
time use.
3. The best storage environment of the device is -
20ºC to 70ºC ambient temperature and not higher
than 95% relative humidity.
4. Users are advised to calibrate the device termly (or
according to the calibrating program of hospital).
It also can be performed at the state-appointed
agent or just contact us for calibration.
Note: 1. Do not sterilize, autoclave or immerse this
device in liquid. Do not pour or spray any
liquids onto the device.
2. Do not use caustic or abrasive cleaning
agents, or any cleaning agent containing
ammonium chloride or isopropyl alcohol.
Symptoms Check points Corrections
SpO2 or
pulse rate
cannot
displayed
Applied nger
improperly.
Place the nger prop-
erly and try again.
SpO2 is too low to
detect
Try again; go to con-
sult with your physi-
cian if you are sure the
device works well.
SpO2 or
pulse rate are
not displayed
stably
Applied nger
improperly.
Place the nger prop-
erly and try again.
Finger is shaking
or body is moving. keep body steady
No display
when button
is pressed
Batteries run
down
Replace with new
batteries
Batteries not
inserted correctly. Re-insert batteries
The display
disappears
suddenly
The device will
auto power o
when it gets no
signal.
Normal
Low battery Replace with new
batteries
Note: If the unit does not work, return it to your
dealer. Under no circumstance should
you disassemble and repair the unit by
yourself.
SpO2
Measuring range 35%~99%, (the resolution is 1%).
Accuracy 70%~99%: ±2%, Below 35~69%:
unspecied.
Optical Sensor Red light (wavelength is 660nm),
Infrared (wavelength is 905/880nm)
Pulse
Measuring range 30bpm~250bpm (the resolution is 1
bpm)
Accuracy ±3bpm
Power source AAA × 2 (Alkaline)
Battery life Continually for 16 hours with two
alkaline batteries
Operating
Condition
Temperature: 5ºC~40ºC (41ºF ~ 104ºF),
Relative Humidity: 15-95% (non
condensing), Atmospheric pressure:
700hPa ~ 1013hkPa, Attitude: -1,280 to
12,000 feet (-390m to 3,658m)
Storage
Condition
Temperature: -25ºC~+70ºC(-13ºF ~
158ºF), Relative humidity: 15-90%(non
condensing), Atmospheric pressure:
700hPa ~ 1013hkPa, Attitude: -1,280 to
12,000 feet (-390m to 3,658m),
The time from 70ºC or -25ºC back to
use : 3 hours
Dimensions 63.5(L) × 34W) × 35(H) mm
Weight About 37g (without the batteries)
Standards IEC60601-1-2, Class B, IEC60601-1, Type
BF, ISO80601-2-61, MDD 93/42/EEC
Type BF applied parts
IP Classication IP22: Protection against harmful
ingress of water and particulate matter
Report No.: 17-02-RBO-033
cluding children) with restricted physical, sensory
or mental skills or a lack of experience and/or a lack
of knowledge, unless they are supervised by a per-
son who has responsibility for their safety or they
receive instructions from this person on how to use
the device. Children should be supervised around
the device to ensure they do not play with it.
- Neither of the displays for the pulse wave and pulse
bar allows the strength of the pulse or circulation to
be evaluated at the measurement site. Rather, they
are exclusively used to display the current signal
variation at the measurement site and do not en-
able reliable diagnostics for the pulse.
- A warning that other cables and accessories may
negatively aect EMC performance.
- A warning regarding stacking and location close to
other equipment.
- A warning that use of other accessories results in
non-compliance.
- The maximum temperature might reach 41.9°C
when operating for long time.
- The safety way for all people use is measuring for
10minutes, and turn it o for 20 minustes before
measure again.
Model: SB100
www.rossmax.com
Fingertip Pulse Oximeter
IN0SB100000000211 RI_IB_SB100_EN_TP_ver1803
Warranty Card
This instrument is covered by a 1 year guarantee from the date of purchase, batteries
and accessories are not included.The guarantee is valid only on presentation of the
guarantee card completed by the dealer confirming date of purchase or the receipt.
Opening or altering the instrument invalidates the guarantee. The guarantee does
not cover damage, accidents or non-compliance with the instruction manual. Please
contact your local seller/dealer or www.rossmax.com.
Customer Name: __________________________________
Address: _______________________________________
Telephone: _____________________________________
E-mail address: ___________________________________
Product Information: ______________________________
Date of purchase: _________________________________
Store where purchased:
______________________________________________
Rossmax InnoTek Corp.
12F., No. 189, Kang Chien Rd.,Taipei, 114,Taiwan.
CMC Medical Devices & Drugs S.L.
C/ Horacio Lengo Nº 18, CP 29006, Málaga, Spain
WARNING: The symbol on this product means that it's an electronic product
and following the European directive 2012/19/EU the electronic products have
to be dispose on your local recycling centre for safe treatment.
EMC guidance and manufacturer’s declaration
Recommended separation distances between portable and mobile RF communications equipment and the ME equipment
The Finger-tip pulse oximeter is intended for use in an electromagnetic environment in which radiated RF disturbances are con-
trolled.The customer or the user of the Finger-tip pulse oximeter can help prevent electromagnetic interference by maintaining a
minimum distance between portable and mobile RF communications equipment (transmitters) and the Finger-tip pulse oximeter
as recommended below, according to 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=[3.5/
V1]√P 80 MHz to 800 MHz , d=[3.5/ E1]√P 800 MHz to 2,5 GHz , d=[7/ E1]√P
0.01 0.1 0.1 0.2
0.1 0.4 0.4 0.7
11.2 1.2 2.3
10 3.7 3.7 7.4
100 11.7 11.7 23.3
Declaration – electromagnetic emissions
The Finger-tip pulse oximeter is intended for use in the electromagnetic environment specied below.The customer or the user of
the Finger-tip pulse oximeter should assure that it is used in such an environment.
Emissions test Compliance Electromagnetic environment - guidance
RF emissions CISPR 11 Group 1 Portable and mobile RF communications equipment should be used no
closer to any part of the EQUIPMENT or SYSTEM including cables, than the
recommended separation distance calculated from the equation applicable
to the frequency of the transmitter. Interference may occur in the vicinity of
equipment marked with the following symbol.
RF emissions CISPR 11 Class B The Finger-tip pulse oximeter 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 N/A
Voltage uctuations/Flicker emissions
IEC 61000-3-3 N/A
Declaration – electromagnetic emissions and immunity – for EQUIPMENT and SYSTEMS that are use in the professional health-
care facility environment or in the home healthcare environment
The Finger-tip pulse oximeter declaration – electromagnetic immunity
The Finger-tip pulse oximeter system is intended for use in the electromagnetic environment specied below.The customer or
the user of the Finger-tip pulse oximeter system should assure that it is used in such an environment.
Immunity test IEC 60601 test level Compliance level Electromagnetic environment - guidance
Conducted RF IEC
61000-4-6 3 Vrms ; 6Vrms ; 150 kHz to 80 MHz N/A Portable and mobile RF communications equipment should be used no closer to any part of the EQUIPMENT
or SYSTEM including cables, than the recommended
separation distance calculated from the equation ap-
plicable to the frequency of the transmitter. Interference
may occur in the vicinity of equipment marked with the
following symbol.
Radiated RF IEC
61000-4-3 3 V/m ; 10V/m ; 80 MHz – 2.7 GHz l 80% 3 V/m ; 10V/m ; 80 MHz – 2.7 GHz ; 80%
Proximity elds
from RF wireless
Communications
equipment IEC
61000-4-3
27V/m 385 MHz 27V/m 385 MHz
28V/m 450 MHz 28V/m 450 MHz
9V/m 710 MHz 9V/m 710 MHz
745 MHz 745 MHz
780 MHz 780 MHz
28V/m 810 MHz 28V/m 810 MHz
870 MHz 870 MHz
930 MHz 930 MHz
28V/m 1720 MHz 28V/m 1720 MHz
1845 MHz 1845 MHz
1970 MHz 1970 MHz
28V/m 2450 MHz 28V/m 2450 MHz
9V/m 5240 MHz 9V/m 5240 MHz
5500 MHz 5500 MHz
5785 MHz 5785 MHz
Declaration – electromagnetic immunity
The Finger-tip pulse oximeter system is intended for use in the electromagnetic environment specied below.The customer or
the user of the Finger-tip pulse oximeter system should assure that it is used in such an environment.
Immunity test IEC 60601 test level Compliance level Electromagnetic environment - guidance
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
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 IEC 61000-4-4 ±2 kV for power supply lines ±1 kV for input/output lines N/A Mains power quality should be that of a typical commercial or hospital environment.
Surge IEC 61000-4-5 ±0.5 kV
±1 kV dierential mode
±2 kV common mode
N/A 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 IEC
61000-4-11
0 % UT; 0, 5 cycle At 0°, 45°,
90°, 135°, 180°, 225°, 270°
and 315°
0 % UT; 1 cycle And 70
% UT; 25/30 cycle Single
phase: at 0°
N/A Mains power quality should be that of a typical
commercial or hospital environment. If the user
of the EQUIPMENT or SYSTEM requires continued
operation during power mains interruptions, it is
recommended that the EQUIPMENT or SYSTEM
be powered from an uninterruptible power sup-
ply or a battery.
Power frequency (50/60
Hz) magnetic eld IEC
61000-4-8
30 A/m 30 A/m Power frequency magnetic elds should be at
levels characteristic of a typical location in a typi-
cal commercial or hospital environment.

Cleaning and disinfection
Troubleshooting
Specification
1. Please clean the surface of the device before us-
ing. Wipe the device with medical alcohol (70%
isopropyl alcohol)first, and then let it dry in air or
clean it by dry clean fabric. When cleaning the de-
vice with water, the water temperature should be
lower than 60ºC
2. Using the medical alcohol to disinfect the prod-
uct after use, prevent from cross infection for next
time use.
3. The best storage environment of the device is -
20ºC to 70ºC ambient temperature and not higher
than 95% relative humidity.
4. Users are advised to calibrate the device termly (or
according to the calibrating program of hospital).
It also can be performed at the state-appointed
agent or just contact us for calibration.
Note: 1. Do not sterilize, autoclave or immerse this
device in liquid. Do not pour or spray any
liquids onto the device.
2. Do not use caustic or abrasive cleaning
agents, or any cleaning agent containing
ammonium chloride or isopropyl alcohol.
Symptoms Check points Corrections
SpO2 or
pulse rate
cannot
displayed
Applied nger
improperly.
Place the nger prop-
erly and try again.
SpO2 is too low to
detect
Try again; go to con-
sult with your physi-
cian if you are sure the
device works well.
SpO2 or
pulse rate are
not displayed
stably
Applied nger
improperly.
Place the nger prop-
erly and try again.
Finger is shaking
or body is moving. keep body steady
No display
when button
is pressed
Batteries run
down
Replace with new
batteries
Batteries not
inserted correctly. Re-insert batteries
The display
disappears
suddenly
The device will
auto power o
when it gets no
signal.
Normal
Low battery Replace with new
batteries
Note: If the unit does not work, return it to your
dealer. Under no circumstance should
you disassemble and repair the unit by
yourself.
SpO2
Measuring range 35%~99%, (the resolution is 1%).
Accuracy 70%~99%: ±2%, Below 35~69%:
unspecied.
Optical Sensor Red light (wavelength is 660nm),
Infrared (wavelength is 905/880nm)
Pulse
Measuring range 30bpm~250bpm (the resolution is 1
bpm)
Accuracy ±3bpm
Power source AAA × 2 (Alkaline)
Battery life Continually for 16 hours with two
alkaline batteries
Operating
Condition
Temperature: 5ºC~40ºC (41ºF ~ 104ºF),
Relative Humidity: 15-95% (non
condensing), Atmospheric pressure:
700hPa ~ 1013hkPa, Attitude: -1,280 to
12,000 feet (-390m to 3,658m)
Storage
Condition
Temperature: -25ºC~+70ºC(-13ºF ~
158ºF), Relative humidity: 15-90%(non
condensing), Atmospheric pressure:
700hPa ~ 1013hkPa, Attitude: -1,280 to
12,000 feet (-390m to 3,658m),
The time from 70ºC or -25ºC back to
use : 3 hours
Dimensions 63.5(L) × 34W) × 35(H) mm
Weight About 37g (without the batteries)
Standards IEC60601-1-2, Class B, IEC60601-1, Type
BF, ISO80601-2-61, MDD 93/42/EEC
Type BF applied parts
IP Classication IP22: Protection against harmful
ingress of water and particulate matter
Report No.: 17-02-RBO-033
cluding children) with restricted physical, sensory
or mental skills or a lack of experience and/or a lack
of knowledge, unless they are supervised by a per-
son who has responsibility for their safety or they
receive instructions from this person on how to use
the device. Children should be supervised around
the device to ensure they do not play with it.
- Neither of the displays for the pulse wave and pulse
bar allows the strength of the pulse or circulation to
be evaluated at the measurement site. Rather, they
are exclusively used to display the current signal
variation at the measurement site and do not en-
able reliable diagnostics for the pulse.
- A warning that other cables and accessories may
negatively aect EMC performance.
- A warning regarding stacking and location close to
other equipment.
- A warning that use of other accessories results in
non-compliance.
- The maximum temperature might reach 41.9°C
when operating for long time.
- The safety way for all people use is measuring for
10minutes, and turn it o for 20 minustes before
measure again.
Model: SB100
www.rossmax.com
Fingertip Pulse Oximeter
IN0SB100000000211 RI_IB_SB100_EN_TP_ver1803
Warranty Card
This instrument is covered by a 1 year guarantee from the date of purchase, batteries
and accessories are not included.The guarantee is valid only on presentation of the
guarantee card completed by the dealer confirming date of purchase or the receipt.
Opening or altering the instrument invalidates the guarantee. The guarantee does
not cover damage, accidents or non-compliance with the instruction manual. Please
contact your local seller/dealer or www.rossmax.com.
Customer Name: __________________________________
Address: _______________________________________
Telephone: _____________________________________
E-mail address: ___________________________________
Product Information: ______________________________
Date of purchase: _________________________________
Store where purchased:
______________________________________________
Rossmax InnoTek Corp.
12F., No. 189, Kang Chien Rd.,Taipei, 114,Taiwan.
CMC Medical Devices & Drugs S.L.
C/ Horacio Lengo Nº 18, CP 29006, Málaga, Spain
WARNING: The symbol on this product means that it's an electronic product
and following the European directive 2012/19/EU the electronic products have
to be dispose on your local recycling centre for safe treatment.
EMC guidance and manufacturer’s declaration
Recommended separation distances between portable and mobile RF communications equipment and the ME equipment
The Finger-tip pulse oximeter is intended for use in an electromagnetic environment in which radiated RF disturbances are con-
trolled.The customer or the user of the Finger-tip pulse oximeter can help prevent electromagnetic interference by maintaining a
minimum distance between portable and mobile RF communications equipment (transmitters) and the Finger-tip pulse oximeter
as recommended below, according to 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=[3.5/
V1]√P 80 MHz to 800 MHz , d=[3.5/ E1]√P 800 MHz to 2,5 GHz , d=[7/ E1]√P
0.01 0.1 0.1 0.2
0.1 0.4 0.4 0.7
11.2 1.2 2.3
10 3.7 3.7 7.4
100 11.7 11.7 23.3
Declaration – electromagnetic emissions
The Finger-tip pulse oximeter is intended for use in the electromagnetic environment specied below.The customer or the user of
the Finger-tip pulse oximeter should assure that it is used in such an environment.
Emissions test Compliance Electromagnetic environment - guidance
RF emissions CISPR 11 Group 1 Portable and mobile RF communications equipment should be used no
closer to any part of the EQUIPMENT or SYSTEM including cables, than the
recommended separation distance calculated from the equation applicable
to the frequency of the transmitter. Interference may occur in the vicinity of
equipment marked with the following symbol.
RF emissions CISPR 11 Class B The Finger-tip pulse oximeter 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 N/A
Voltage uctuations/Flicker emissions
IEC 61000-3-3 N/A
Declaration – electromagnetic emissions and immunity – for EQUIPMENT and SYSTEMS that are use in the professional health-
care facility environment or in the home healthcare environment
The Finger-tip pulse oximeter declaration – electromagnetic immunity
The Finger-tip pulse oximeter system is intended for use in the electromagnetic environment specied below.The customer or
the user of the Finger-tip pulse oximeter system should assure that it is used in such an environment.
Immunity test IEC 60601 test level Compliance level Electromagnetic environment - guidance
Conducted RF IEC
61000-4-6 3Vrms ; 6 Vrms ; 150 kHz to 80 MHz N/A Portable and mobile RF communications equipment should be used no closer to any part of the EQUIPMENT
or SYSTEM including cables, than the recommended
separation distance calculated from the equation ap-
plicable to the frequency of the transmitter. Interference
may occur in the vicinity of equipment marked with the
following symbol.
Radiated RF IEC
61000-4-3 3V/m ; 10V/m ; 80 MHz – 2.7 GHz l 80% 3 V/m ; 10V/m ; 80 MHz – 2.7 GHz ; 80%
Proximity elds
from RF wireless
Communications
equipment IEC
61000-4-3
27V/m 385 MHz 27V/m 385 MHz
28V/m 450 MHz 28V/m 450 MHz
9V/m 710 MHz 9V/m 710 MHz
745 MHz 745 MHz
780 MHz 780 MHz
28V/m 810 MHz 28V/m 810 MHz
870 MHz 870 MHz
930 MHz 930 MHz
28V/m 1720 MHz 28 V/m 1720 MHz
1845 MHz 1845 MHz
1970 MHz 1970 MHz
28V/m 2450 MHz 28 V/m 2450 MHz
9V/m 5240 MHz 9 V/m 5240 MHz
5500 MHz 5500 MHz
5785 MHz 5785 MHz
Declaration – electromagnetic immunity
The Finger-tip pulse oximeter system is intended for use in the electromagnetic environment specied below.The customer or
the user of the Finger-tip pulse oximeter system should assure that it is used in such an environment.
Immunity test IEC 60601 test level Compliance level Electromagnetic environment - guidance
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
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 IEC 61000-4-4 ±2 kV for power supply lines ±1 kV for input/output lines N/A Mains power quality should be that of a typical commercial or hospital environment.
Surge IEC 61000-4-5 ±0.5 kV
±1 kV dierential mode
±2 kV common mode
N/A 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 IEC
61000-4-11
0 % UT; 0, 5 cycle At 0°, 45°,
90°, 135°, 180°, 225°, 270°
and 315°
0 % UT; 1 cycle And 70
% UT; 25/30 cycle Single
phase: at 0°
N/A Mains power quality should be that of a typical
commercial or hospital environment. If the user
of the EQUIPMENT or SYSTEM requires continued
operation during power mains interruptions, it is
recommended that the EQUIPMENT or SYSTEM
be powered from an uninterruptible power sup-
ply or a battery.
Power frequency (50/60
Hz) magnetic eld IEC
61000-4-8
30 A/m 30 A/m Power frequency magnetic elds should be at
levels characteristic of a typical location in a typi-
cal commercial or hospital environment.