9 TROUBLESHOOTING
Trouble
Possible Reason
Solution
The SpO
2
and Pulse
Rate cannot
be displayed
normally
1. The finger is not properly
positioned.
2. The user’s SpO
2
is too
low to be detected.
1. Place the finger properly
and try again.
2. Go to a hospital for a
diagnosis if you are sure
the oximeter is working
correctly.
The Sp0
2
and
Pulse Rate are
not displayed
stably
1. The finger is not placed
inside deep enough.
2. The finger is shaking or
the user is moving
1. Place the finger properly
and try again.
2. Remain still while taking
the measurement
The oximeter
cannot be
turned on
1. The batteries are drained
or almost drained.
2. The batteries are not
inserted properly.
3. Malfunction of the
oximeter.
1. Change batteries.
2. Reinstall batteries.
3. Please contact customer
support.
The display is
off suddenly
1. The product will enter
standby mode when no
signal is in the product
within 5 seconds.
2. The batteries are almost
drained.
1. Normal.
2. Change batteries.
10 KEY OF SYMBOLS
Symbol
Description
Symbol
Description
Type BF
WEEE (2002/96/EC)
Refer to instruction
manual
IP22
Ingress of liquids rank
%SpO
2
The pulse oxygen
saturation (%)
Manufacturer
PRbpm
Pulse rate (bpm)
Manufacture Date
Full-voltage
Storage and
Transport
Temperature
limitation
The battery voltage
indication is deficient
(change the battery
in time avoiding the
inexact measure)
Storage and
Transport Humidity
limitation
1. No finger inserted
2. An indicator of
signal inadequacy
Storage and
Transport
Atmospheric pressure
limitation
Battery positive
electrode
This side UP
Battery cathode
Fragile, handle with
care
1. Exit standby mode.
2. Change brightness
of the screen.
Keep dry
SN
Serial number
Recyclable
Alarm inhibit
11 FUNCTION SPECIFICATION
Display Information
Display Mode
The Pulse Oxygen
Saturation (SpO
2
)
LCD
Pulse Rate (PR)
LCD
Pulse Intensity (bar-graph) LCD bar-graph display
Pulse Wave
LCD
SpO
2
Parameter Specification
Measuring Range
0% ~ 100%, (the resolution is 1%).
Accuracy
70% ~ 100%: ±2% ,Below 70% unspecified.
Optical Sensor
Red light (wavelength is 660 nm)
Infrared (wavelength is 880 nm)
Pulse Parameter Specification
Measuring Range
30 bpm ~ 250 bpm (the resolution is 1 bpm)
Accuracy
±2 bpm or ±2% select larger
Pulse Intensity
Range
Continuous bar-graph display, the higher
display indicate the stronger pulse.
Battery Requirement
1.5V (AAA size) alkaline batteries × 2 or rechargeable battery
Battery Useful Life
Two batteries can work continually for 24 hours
Dimensions and Weight
Dimensions
2.3 (L) x 1.3 (W) x 1.3 (H) inch / 59(L) × 33(W)
× 32(H) mm
Weight
~ 2 oz / 57 g (with the batteries)
12 APPENDIX
Guidance and manufacture’s declaration – electromagnetic emissions
for all EQUIPMENT and SYSTEMS
Guidance and Manufacture’s Declaration – Electromagnetic Emission
The
UP-200 Pulse Oximeter
is intended for use in the electromagnetic
environment specified below. The customer of the user of the
UP-200 Pulse
Oximeter
should assure that it is used in such and environment.
Emission test
Compliance
Electromagnetic Environment –
Guidance
RF emission
CISPR 11
Group 1
The
UP-200 Pulse Oximeter
uses RF
energy only for its internal function.
Therefore, its RF emissions are very
low and are not likely to cause any
interference in nearby electronic
equipment.
RF emission
CISPR 11
Class B
The
UP-200 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
fluctuations/
flicker emissions
IEC 61000-3-3
N/A
Guidance and manufacture’s declaration – electromagnetic immunity
for all EQUIPMENT and SYSTEMS
Guidance and Manufacture’s Declaration – Electromagnetic Immunity
The
UP-200 Pulse Oximeter
is intended for use in the electromagnetic
environment specified below. The customer or the user of
UP-200 Pulse
Oximeter
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
±6 kV contact
±8 kV air
±6 KV contact
±8 kV air
Floors should be wood,
concrete or ceramic tile.
If floor is covered with
synthetic material, the
relative humidity should
be at least 30%.
Power
frequency
(50/60Hz)
Magnetic field
IEC-61000-
4-8
3 A/m
3 A/m
Power frequency
magnetic fields
should be at levels
characteristic of a typical
location in a typical
commercial or hospital
environment.
Guidance and manufacture’s declaration – electromagnetic immunity
for EQUIPMENT and SYSTEMS that are not LIFE-SUPPORTING
Guidance and manufacture’s declaration – electromagnetic immunity
The
UP-200 Pulse Oximeter
is intended for use in the electromagnetic
environment specified below. The customer or the user of
UP-200 Pulse
Oximeter
should assure that it is used in such an environment.
Immunity
Test
IEC
60601
Test
Level
Compliance
Level
Electromagnetic Environment -
Guidance
Radiated
RF
IEC 61000-
4-3
3 V/m
80 MHz
to 2.5
GHz
3 V/m
Portable and mobile RF
communications equipment should be
used no closer to any part of the
UP-
200 Pulse Oximeter
, including cables,
than the recommended separation
distance calculated from the equation
applicable to the frequency of the
transmitter.
Recommended separation distance
80 MHz to 800 MHz
800 MHz to 2.5 GHz
Where P is the maximum output
power rating of the transmitter
in watts (W) according to the
transmitter manufacturer and d is the
recommended separation distance in
meters (m). Field strengths from fixed
RF transmitters, as determined by an
electromagnetic site survey,
a
should
be less than the compliance level in
each frequency range.
b
Interference
may occur in the vicinity of equipment
marked with the following symbol:
NOTE 1: At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic
propagation is affected by absorption and reflection from structures, objects
and people.
a
Field strengths from fixed transmitters, such as base stations for radio
(cellular/cordless) telephones and land mobile radios, amateur radio, AM
and FM radio broadcast and TV broadcast cannot be predicted theoretically
with accuracy. To assess the electromagnetic environment due to fixed RF
transmitters, an electromagnetic site survey should be considered. If the
measured field strength in the location in which the
UP-200 Pulse Oximeter
is used exceeds the applicable RF compliance level above, the
UP-200
Pulse Oximeter
should be observed to verify normal operation. If abnormal
performance is observed, additional measures may be necessary, such as
reorienting or relocating the
UP-200 Pulse Oximeter
.
b
Over the frequency range 150 kHz to 80 MHz, field strengths should be less
than 3 V/m.
©2020 A&D Medical. All rights reserved.
Specifications subject to change without notice.
Recommended separation distances between portable and mobile RF
communications equipment and the EQUIPMENT or SYSTEM
for EQUIPMENT or SYSTEM that are not LIFE-SUPPORTING
Recommended separation distances between portable and mobile RF
communications equipment and the UP-100CN
The
UP-200 Pulse Oximeter
is intended for use in an electromagnetic
environment in which radiated RF disturbances are controlled. The
customer or the user of the
UP-200 Pulse Oximeter
can help prevent
electromagnetic interference by maintaining a minimum distance between
portable and mobile RF communications equipment (transmitters) and the
UP-200 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
80 MHz to 800
MHz
800 MHz to 2.5
GHz
0.01
0.12
0.12
0.23
0.1
0.39
0.37
0.74
1
1.17
1.17
2.33
10
3.69
3.69
7.38
100
11.67
11.67
23.33
For transmitters rated at a maximum output power not listed above, the
recommended separation distance d in meters (m) can be estimated using
the equation applicable to the frequency of the transmitter, where P is the
maximum output power rating of the transmitter in watts (W) according to
the transmitter manufacturer.
NOTE 1: At 80 MHz and 800 MHz, the separation distance for the higher
frequency range applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic
propagation is affected by absorption and reflection from structures, objects
and people.
13 WARRANTY
Limited Warranty:
A&D Medical (“A&D”) warrants to the first purchaser (“You”) that the A&D
product You purchased (the “Product”) will be free from defects in material,
workmanship and design for the applicable Warranty Term stated above from
the date You purchased the Product under normal use. This Limited Warranty
is personal to You and is not transferable. If the Product is defective, then (i)
if You are a Consumer, You return the Product to the retailer You purchased
it from (if within such retailer’s return time frame) or You return it to A&D
in accordance with the procedure set forth below, or (ii) if You are NOT a
Consumer, You return the Product to A&D in accordance with the procedure
set forth below. A&D’s warranty obligation is limited to the repair or
replacement, at A&D’s option, of the defective Product that has been returned
by You within the warranty period. Such repair or replacement will be at no
charge to You. The repaired or replacement Product is warranted hereunder
for the longer of the remainder of the original warranty period or 90 days from
the date of shipment of the repaired or replacement Product. If you return the
Product for warranty service to A&D, You must return the Product, freight and
insurance prepaid, within the warranty period to the address set forth below,
together with satisfactory proof of the date of Your purchase (such as a sales
receipt or statement of online warranty registration) and a description of the
defect. Also please enclose a check for return shipping and insurance of the
Product, as provided to you by the customer service representative.
In the United States of America:
2 year warranty
A&D Engineering, Inc.
1756 Automation Parkway
San Jose, CA 95131 U.S.A.
www.andmedical.com
1-888-726-9966
In Canada:
2 year warranty
Auto Control Medical, Inc.
6695 Millcreek Drive, Unit 6 Mississauga,
Ontario, L5N 5R8 Canada
www.lifesourcecanada.com
1-800-461-0991
In Latin America
Please return to your local dealer.
CONTACT INFORMATION
Manufactured by:
Contec Medical Systems Co., Ltd.
No.112 Qinhuang West Street, Economic & Technical Development Zone,
Qinhuangdao, Hebei Province, PEOPLE’S REPUBLIC OF CHINA
Manufactured for:
A&D Engineering, Inc.
1756 Automation Parkway
San Jose, CA 95131 USA
andmedical.com
1-888-726-9966
Distributed in Canada by:
Auto Control Médical an A&D Company / une compagnie A&D
6695 Millcreek Drive, Unit 6
Mississauga, Ontario
L5N 5R8 Canada
lifesourcecanada.com
1-800-461-0991
