Cleaning
Maintenance
T
Specification
1.
Wipe the device with medical alcohol (70% isopro-
pyl alcohol)first, and then let it dry in air or clean it
by dry clean fabr
water
60°C
2.
after use, prevent fr
use.
3.
to 70°C ambient temperature and not higher than
90% relative humidity
Note: -
vice in liquid. Do not pour or spray any liquids
onto the device.
2. not use caustic or abrasive cleaning
agents, or any cleaning agent containing am-
monium chloride or isopropyl alcohol.
Recommends user to return this device to the man-
ufacturer per
months.
- -
al damage or deterioration.
- -
tion normally.
Note:
to verify operation of the pulse oximeter equip-
ment.
Symptoms Check points Corrections
SpO2 or
pulse rate
cannot
displayed
Applied nger
improperly
Place the nger prop-
erly and tr
SpO2 is too low to
detect
T-
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 tr
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-inser
The display
disappears
suddenly
The device will
auto power o
when it gets no
signal.
Normal
Low battery Replace with new
batteries
dealer
disassemble and repair the unit by yourself
SpO2
Measuring
range
35%~99%, (the resolution is 1%).
Accuracy 70%~99%: ±2%, Below 35~69%:
unspecied.
Optical Sensor The wavelength of red LED is 660 nm
and Infrared LED is 905/880 nm with
maximum optical output power of 4
mW/sr
Pulse
Measuring
range
30 bpm~250 bpm (the resolution is 1
bpm)
Accuracy ±3 bpm
Pow AAA × 2 (Alkaline)
Battery life Continually for 16 hours with two alkaline
batteries
Operating
Condition
T°F ~ 104°F),
Relative Humidity
condensing), Atmospheric pressure:
700hPa ~ 1060hP
12,000 feet (-390m to 3,658m)
Storage /
T
Condition
T°C~+70°C(-13°F ~
158°F), Relative humidity
condensing), Atmospheric pressure:
700hPa ~ 1060hP
12,000 feet (-390m to 3,658m),
from 70°C or -25°C back to use : 3 hours
Dimensions 63.5(L) × 34W
Weight About 37g (without the batt
Standards IEC60601-1-2, Class B, IEC60601-1,
ISO80601-2-61, IEC/EN60601-1-11
T
IP Classication IP22: Pr
water and particulate matter
Note:
- -
ted SpO2 and pulse rate:
-
pulse rate.
- Data update delay: Less than 2 seconds.
be evaluated at the measurement site. Rather
are exclusively used t-
ation at the measurement site and do not enable r-
liable diagnostics for the pulse
-
negatively aect EMC performance.
-
other equipment.
-
non-compliance.
-
user will touch might reach 42°C when operating in
the 40°C environment.
-
minutes, and turn it o for 20 minut-
ure again.
-
there is no need to calibrate it during its lif
Model: SB100
ww
Fingertip Pulse Oximeter
Rossmax Inno
12F
114, T
CMC Medical Devices & Drugs S.L.
C/ Horacio Lengo Nº 18, CP 29006,
Málaga, Spain
WARNING:
and following the Eur
to be dispose on your local r
EMC guidance and manufacturer’s declaration
Recommended separation distances between portable and mobile RF communications equipment and the ME equipment
The Finger-tip pulse oximet-
trolled.
minimum distance between portable and mobile RF communications equipment (transmitters) and the Finger-tip pulse o
as recommended below
Rated maximum output
power of transmitter /
Separation distance accor
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 oximet
the Finger-tip pulse oximeter should assur
Emissions test Compliance Electr
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 distanc
to the frequency of the transmitter
equipment marked with the following symbol.
RF emissions CISPR 11 Class B The Finger-tip pulse oximet
including domestic establishments and those directly connected to the
public low-voltage power supply network tha
for domestic purposes.
Harmonic emissions IEC 61000-3-2 N/A
Voltage uctuations/F
IEC 61000-3-3 N/A
Declaration – electromagnetic emissions and immunity – for EQUIPMENT and SYSTEMS that are use in the pr-
care facility environment or in the home healthc
The Finger-tip pulse oximet
The Finger-tip pulse oximet
the user of the Finger-tip pulse oximeter system should assur
Immunity test IEC 60601 test level Compliance level Electromagnetic environmen
Conducted RF IEC
61000-4-6 3
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 r
separation distance calculat-
plicable to the frequency of the transmitter
may occur in the vicinity of equipment marked with the
following symbol.
Radiated RF IEC
61000-4-3 3
MHz – 2.7 GHz l 80% 3
MHz – 2.7 GHz ; 80%
Proximity elds
from RF wireless
Communications
equipment IEC
61000-4-3
27 V/m 385 MHz 27 V/m 385 MHz
28 V/m 450 MHz 28 V/m 450 MHz
9 V/m 710 MHz 9 V/m 710 MHz
745 MHz 745 MHz
780 MHz 780 MHz
28 V/m 810 MHz 28 V/m 810 MHz
870 MHz 870 MHz
930 MHz 930 MHz
28 V/m 1720 MHz 28 V/m 1720 MHz
1845 MHz 1845 MHz
1970 MHz 1970 MHz
28 V/m 2450 MHz 28 V/m 2450 MHz
9 V/m 5240 MHz 9 V/m 5240 MHz
5500 MHz 5500 MHz
5785 MHz 5785 MHz
Declaration – electromagnetic immunity
The Finger-tip pulse oximet
the user of the Finger-tip pulse oximeter system should assur
Immunity test IEC 60601 test level Compliance level Electromagnetic envir
Electrostatic discharge
(ESD) IEC 61000-4-2 ±8 kV contact
±2 kV
±15 kV air
±8 kV contact
±2 kV
kV
Floors should be wood, concr
If oors are cover
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 envir
Surge IEC 61000-4-5 ±0.5 kV
±1 kV dierential mode
±2 kV common mode
N/A Mains power quality should be that of a typical
commercial or hospital envir
Voltage dips
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 envir
of the EQUIPMENT or SYSTEM requir
operation during power mains int
recommended that the EQUIPMENT or SY
be powered fr-
ply or a battery.
Power fr
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 envir
IN0SB100000000252
Warranty Card
This instrument is c
and accessories ar
guarantee car
Opening or altering the instrument inv
not cover damage
contact your local seller/dealer or www
Customer Name: __________________________________
Address: _______________________________________
T _____________________________________
E-mail address: ___________________________________
Product Information: ______________________________
Date of purchase: _________________________________
Store where purchased:
______________________________________________
RI_IB_SB100_EN_
2Yr_TP_v
