Creative PC-60N User manual

User Manual for Fingertip Oximeter
I
Instructions to User
Dear Users,
Thank you very much for purchasing our product. Please
read the manual very carefully before using this device.
Failure to follow these instructions can cause measuring
abnormality or damage to the oximeter.
The manual is published in English and we have the
ultimate right to explain the Manual. No part of this
manual may be photocopied, reproduced or translated into
another language without the prior written consent. We
reserve the right to improve and amend it at any time
without prior notice.
Version of the Manual: Ver 1.1
Revised date: July 19, 2012
All rights reserved.
3502-2290049

User Manual for Fingertip Oximeter
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Warnings
Check the device to make sure that there is no
visible damage that may affect user’s safety or
measurement performance with regard to sensors
and clips. It is recommended that the device
should be inspected minimally once a week.
When there is obvious damage, stop using the
device.
Special attention should be paid while the
oximeter is used continuously under the ambient
temperature exceeds 37°, burning hurt may occur
because of over-heating on the sensor.
An uncomfortable or painful feeling may appear
if using the oximeter continuously on the same
place for a long time, especially for poor
microcirculation patients.
It is recommended that the oximeter should not
be applied to the same location for longer than 2
hours. If any abnormal condition is found, please
change the position of oximeter.
Avoid placing the device on the same limb which
is wrapped with a cuff for blood pressure
measurement or during venous infusion.

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DO NOT clip this device on edema or tender
tissue.
The light (the infrared light is invisible) emitted
from the device is harmful to the eyes, so service
technician or testee should not stare at the light.
The oximeter is not a treatment device.
When disposing of the monitor and its
accessories, the local law should be followed.
Instructions for Operation
The finger should be put in properly and correctly.
Do not shake the finger. Keep at ease during
measurement.
Do not put wet finger directly into sensor.
Avoid placing the device on the same limb which
is wrapped with a cuff for blood pressure
measurement or during venous infusion.
Do not let anything block the emitting light from
device.
Vigorous exercise and electrosurgical device
interference may affect the measuring accuracy.
Using enamel or other makeup on the nail may
affect the accuracy of measurement, too long
fingernail may cause failure of measurement or

User Manual for Fingertip Oximeter
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inaccuracy measurement result.
Keep the oximeter away from dust, vibration,
corrosive substances, explosive materials, high
temperature and moisture.
Existence of high intensive light sources, such as
fluorescence light, ruby lamb, infrared heater or
strong sunshine, etc. may cause inaccuracy of
measurement result. Please put an opaque cover
on the sensor or change the measuring site.
If the first reading appears with poor waveform
(irregular or not smooth), then the reading is
unlikely true, the more stable value is expected
by waiting for a while, or a restart is needed when
necessary.

User Manual for Fingertip Oximeter
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Declaration of Conformity:
The manufacturer hereby declares that this
device complies with the following standards:
IEC 60601-1
IEC 60601-1-2
ISO 9919
and follows the provisions of the council
directive
MDD 93/42 EEC
Caution:
U.S. federal law restricts this device to sale or
use by or on the order of a physician.

User Manual for Fingertip Oximeter
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Content
1 Overview.....................................................................1
1.1 Appearance...........................................................1
1.2 Name and Model ..................................................2
1.3 Intended Use.........................................................2
1.4 Structure and Conformation ...............................2
1.5 Features.................................................................2
2 Battery Installation.....................................................3
3 Operation....................................................................4
3.1 Directly Measurement..........................................4
3.2 Over-limit indication and Beep Silence...............7
3.3 Setup Menu Screen...............................................8
3.4 External SpO2Probe Connection......................10
4. Technical Specifications .......................................... 11
5. Accessories ...............................................................14
6. Repair and Maintenance.........................................14
6.1 Oximeter Maintenance.......................................14

User Manual for Fingertip Oximeter
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6.2 Cleaning and Disinfecting Instruction..............16
7. Troubleshooting.......................................................17
Appendix......................................................................18
A Key of Symbols......................................................18
B SpO2Common Knowledge..................................... 19

User Manual for Fingertip Oximeter
1
1 Overview
1.1 Appearance
Figure 1 Front/Rear View

User Manual for Fingertip Oximeter
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1.2 Name and Model
Name: Fingertip Oximeter
Model: PC-60N
1.3 Intended Use
This Fingertip Oximeter is intended for measuring the
pulse rate and functional oxygen saturation (SpO2)
through patient’s finger. It is applicable for spot-checking
SpO2and pulse rate of adult and pediatric patients in
homes and clinics.
1.4 Structure and Conformation
It consists of main unit and photoelectric sensor, and
additional data upload connector.
1.5 Features
• External pediatric SpO2probe available
• Large true color OLED display of SpO2, PR Pulse
Bar, PI & Plethysmogram
• Innovative 4 directions display
• Automatic power on/off
• Audible & visible over-limit indication, high & low
limits are adjustable

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• Shift parameter display between PR and PI
• 2AAA alkaline batteries with low power consumption
• Low battery voltage indication
2 Battery Installation
Figure 2 Battery Installation
1. Refer to Figure2, insert two AAA size batteries into
the battery compartment properly.
2. Replace the cover.
Please make sure that the batteries are correctly
installed, or incorrect installation may cause the
device not to work.

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3 Operation
3.1 Directly Measurement
1. Open the clip as shown in Figure 3.
Figure 3 Put finger into the Oximeter
2. Put finger into the rubber cushions of the clip (make
sure the finger is in the correct position), and then
clip the finger.
3. The device will power on automatically in 2 seconds,
and start to display software version number.
4. Next enter into data display screen (as shown in
Figure 4). User can read the values and view the
waveform from display screen.
Shift parameter display between PR and PI during
measurement:
Short time press Display Key, the display orientation will
rotate 90 degree, at the same time, PR value is shifted to
PI value automatically (as shown in 4B). When shown as
4B, the display will shift to 4C automatically after 20
seconds without operation. Press the key again, the screen

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will change another direction (as shown in 4D). It
obviously shows that shifting parameter between PR and
PI is under the condition of the display orientation
rotating to a side, as shown in 4B and 4E. After 20
seconds without operation, the PI will automatically shift
back to PR, as shown in 4C and 4F.
Figure4A Figure4B
Figure4C Figure4D
Figure4E Figure4F

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Screen Description:
“%SpO2”: SpO2symbol; “99”: SpO2 value;
“PR”: Pulse Rate icon; “65”: Pulse Rate value;
“”: Pulse beat symbol;
“”: Pulse intensity bar graph.
“PI%”: Perfusion index icon; “1.4”: Perfusion
Index value;

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3.2 Over-limit indication and Beep Silence
When measuring, if SpO2value or pulse rate value
exceeds the preset alarm limit, the device will beep
automatically and the value which exceeds limit on the
screen will flash. The detailed information refers to
chapter 4.
When the beep sound is activated by over-limit, it will
become silence at the following situations:
1. When SpO2and PR value return to normal range.
2. Press Display Key to mute. If this over-limit
event continues, the oximeter will resume beeping
automatically later in 2 minutes.
3. Remove the finger from the oximeter or SpO2
probe.

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3.3 Setup Menu Screen
Figure 5 Menu Screen
Long time pressing display key could enter the setup
menu screen.
Setup Menu Screen Description：
“SpO2alm Lo
”
：SpO2lower limit. The user can
modify the value within 85~99, the step is “1”, the
default is 90.
“PR alm Hi”：Pulse Rate high limit. The user can
modify the value within 100~240, the step is “5”, the
default is 120.

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“PR alm Lo”：Pulse Rate low limit. The user can
modify the value within 30~60, the step is “1”, the
default is 50.
“Pulse beep”：Pulse beep option. If it is set to on, every
pulse beat makes a beep, and the pitch tone of this beep
changes according to SpO2 value (within 90~99%).
“Save, exit menu”：Long time pressing this item
to store settings and exit from the setup menu to the
normal display screen.
“Restore default”：Restore default setting. Refer to
Figure 5 for each default value.
On setup menu screen:
1. Short time press Display Key to choose the
setting item;
2. Longtime press Display Key to active the setting
item, then short time press it to modify the setting
parameter;
3. Next, longtime press Display Key to confirm the
modification and exit from this setting item.
4. At last, move the setting item to “Save, exit
menu”, and long time pressing Display Key to
store the modification and exit from the setup
menu.

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3.4 External SpO2Probe Connection
1. Connect the external SpO2probe to SpO2sensor
connector in the following way. Make sure the side
with “Arrow” faces upwards.
Figure 6 Probe Connection
Note: when the external SpO2probe is connected well,
the built-in finger clip sensor will be disabled. The
measurement is detected from the external SpO2probe.
2. The finger should be put in SpO2probe properly and
correctly.
3. The oximeter will power on automatically 2 seconds
later, then display software version number.
4. Other operation is similar to chapter 3.1 directly
measurement.

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4. Technical Specifications
A. Technique: dual-wavelength LED sensor,
LED sensor wavelength:
Red light: 663 nanometers,
Infrared light: 890 nanometers.
Maximal optical output power:
less than 1.5mW maximum average.
B. SpO2measurement
Measuring range: 70%~100%
Measuring accuracy:
Arms is not greater than 3% for SpO2range from
70% to 100%
Note: Arms is defined as root-mean-square value of
deviation according to ISO 9919.
SpO2low limit setting range:
85%~99% (default 90%)
C. Pulse Rate measurement
Measuring range: 30bpm~240bpm
Measuring accuracy: ±2bpm or ±2% (whichever is
greater)
Pulse Rate limit setting range:

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high limit: 100~240bpm (default 120bpm)
low limit: 30~60bpm (default 50bpm)
D. Perfusion Index(PI) Display
Range: 0.2%~20%
E.Audible &visual over-limit indication
When measuring, if SpO2value or pulse rate value
exceeds the preset limit, the device will beep
automatically and the value which exceeds limit
on the screen will flash. The oximeter will shut
down automatically in 8 seconds with no signal.
F. Display mode
：
Color OLED Display
G. Power supply requirement:
2 x LR03 (AAA) alkaline batteries
Supply voltage: 3.0VDC
Operating current: ≤40mA
H. Environment requirement
Operating Temperature: 5 ~40°C
Operating Humidity: 30~80%
Atmospheric pressure: 70~106kPa
I. The performance under low perfusion condition
The accuracy of SpO2and PR measurement still
meets the specification described above when the
modulation amplitude is as low as 0.6%.

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J. Resistance to interference of surrounding light:
The difference between the SpO2 value measured
in the condition of indoor natural light and that of
darkroom is less than ±1%.
K. Dimensions: 60 mm (L) × 33 mm (W) × 30 mm (H)
Net Weight: 35g (including battery)
L. Classification:
The type of protection against electric shock:
Internally powered equipment.
The degree of protection against electric shock:
Type BF applied parts.
The degree of protection against harmful ingress
of liquids: Ordinary equipment without protection
against ingress of water.
Electro-Magnetic Compatibility: Group I, Class B