Maintenance and Storage
1.
Replace the batteries in time when low voltage lamp is lighted.
2.
Clean surface of the fingertip oximeter before it is used in diagnosis for patients.
3.
Remove the batteries inside the battery cassette if the Oximeter will not be
operated for a long time.
4.
It is best to preserve the product in a place where ambient temperatures is
-20
℃～
55
℃
(-4
～
131
℉
) and relative humidity is
≤
93%.
5.
It is recommended that the product should be kept in a dry environment anytime.
A wet ambient might affect its lifetime and even might damage the product.
6.
Please follow the law of the local government to deal with used battery.
Detailed descriptions of product functions
1. Display Type:
LED
2. SpO
2
:
Measurement range: 70-99%
Accuracy: 80%-99%, ±2%; 70%-80%,±3%;
≤
69% no definition.
3. Pulse Rate:
Measure range: 30-235 BPM
Accuracy: 30~99bpm, ±2bpm; 100~235bpm, ±2%
Pulse Intensity: Bargraph Indicator
4. Power Requirements:
Two AAA alkaline Batteries
Power consumption: Less than 40mA
Low power indication:
Battery Life: Two AAA 1.5V, 600mAh alkaline batteries could be continuously operated
as long as 30 hours.
5. Dimension:
Length: 56mm
～
62mm
Width: 32mm
～
38mm
Height: 34mm
～
38mm
Weight: 45g
～
60g (including two AAA batteries)
6. Environment Requirements:
Operation Temperature: 5
～
40
℃
Storage Temperature: -20
～
55
℃
Ambient Humidity:
≤
80%, no condensation in operation.
≤
93%, no condensation in storage
7. Measurement Performance in Low Perfusion Condition:
required the test
equipment (BIO-TEK INDEX Pulse Oximeter tester) the pulse wave is available without
failure when the simulation pulse wave amplitude is at 6%.
8. Interference Resistance Capacity against Ambient Light:
Device works normally
when mixed noise produced by BIO-TEK INDEX Pulse Oximeter tester
.
Declaration
EMC of this product complies with IEC60601-1-2 standard.
The materials which the user can come into contact have no toxicity and no action on
tissues comply with ISO10993-1, ISO10993-5 and ISO10993-10.
Guidance and manufacturer
’s declaration – electromagnetic
emissions-for all EQUIPMENT and SYSTEMS
Guidance and manufacturer
’s declaration – electromagnetic emission
The
Pulse Oximeter
is intended for use in the electromagnetic environment specified
below. The customer or the user of the
Pulse Oximeter
should assure that it is used
in such an environment.
Emission test
Compliance
Electromagnetic environment
– guidance
RF emissions
CISPR 11
Group 1
The
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
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.
Possible Problems and resolutions
Problems
Possible reason
Solution
SpO
2
or PR
can not be
shown
normally
1. Finger is not inserted correctly
2.
Patient’s Oxyhemoglobin value is
too low to be measured
1.Retry by inserting the finger
2. Try some more times, If you
can make sure no problem is
existing in the product.
Please go to a hospital timely
for exact diagnosis.
SpO
2
or PR is
shown
unstably
1. Finger might not be inserted deep
enough.
2.
Finger is trembling or patient’s
body is in movement status.
1. Retry by inserting the finger
2. Try not to move
The Oximeter
can not be
powered on
1. Power of batteries might be
inadequate or not be there at all
2. Batteries might be installed
incorrectly
3. The Oximeter might be damaged
1. Please replace batteries
2. Please reinstall the batteries
3. Please contact with local
customer service centre
Indication
lamps are
suddenly off
1. The product is automatically
powered off when no signal is
detected longer than 8 seconds
2. Power quantity of the batteries is
started being inadequate
1. Normal
2. Replace the batteries
“Error3” or
“Error4” is
displayed on
screen
1. Low power
2. Receiving tube being shielded or
damaged together with broken
connector.
3. Mechanical Misplace for
receive-emission tube
4. Amp circuit malfunctions.
1. Change batteries
2. Please contact local customer
service center
3. Please contact local customer
service center
4 Please contact local
customer service center
“Error7” is
displayed on
screen
1. Low power
2. Emission tube damaged.
3. Current control circuit
malfunctions.
1 Please change battery
2 Please contact local
customer service center
3 Please contact local
customer service center
Symbol Definitions
Symbol
Definition
Type BF applied part.
Attention, consult accompanying documents.
﹪
SpO
2
Oxygen saturation
Heart rate (BPM)
Low power indication
No SpO
2
Alarm
Power switch
SN
Serial No.
Applicable models
MD300C1 MD300C1C MD300C12 MD300C12-P MD300C13 MD300C14
MD300C1-E MD300C15 MD300C16 MD300C17 MD300C18 MD300C19
MD300C10 MD300C1A MD300C1B MD300C1D MD300C1E
Note
：
The illustration used in this manual may differ slightly from the appearance
of the actual product.
ALL RIGHTS RESERVED
Issue date: 25/February 2010