John Bunn JB02017 User manual
1
OXYREAD
FINGERTIP
PULSE OXIMETER
MODEL JB02017
OPERATOR MANUAL
GENERAL DESCRIPTION
The John Bunn
®
JB02017 OxyRead Fingertip Pulse Oximeter
provides a simple way to spot-check users by combining the
sensor and monitor into one integrated, compact, easy to use
device. The oximeter measures pulse oxygen saturation (SpO
2
)
value, pulse rate value, and pulse strength. When a nger
is inserted into the sensor’s rubber cushion, the SpO
2
value
automatically displays. The pulse bar graph displays the user’s
pulse beat, and the bar graph’s height shows pulse strength.
The oximeter, which is powered by two AAA batteries, features
a low-battery indicator and powers off automatically in eight
seconds when not in use.
Product Accessories (Included)
1. One lanyard
2. Two AAA batteries
3. One protective cover
4. One operator manual
Principle of Measurement
Two beams of different wavelength (660 nm glow and 940 nm
near infrared light) are focused onto a human nail tip through a
clamping nger-type sensor. A measured signal obtained by a
photosensitive element, through processes of electronic circuits
and microprocessor, will be shown on the oximeter’s display.
Principle of Operation Diagram
See illustration and descriptions below.
1 Red and Infrared Emission Tube
2 Red and Infrared Receipt Tube
INTENDED USE
The intended use of the OxyRead Fingertip Pulse Oximeter
is the measurement and display of the functional oxygen
saturation of arterial hemoglobin (SpO2) and pulse rate (PR) of
adults and pediatric users in hospital, ambulatory, home, and
EMS (Emergency Medical Service) environments. The Pulse
Oximeter is intended for spot-checking these levels.
Contraindications (
WARNINGS):
• If you do not understand any part of these instructions,
contact a healthcare professional for direction in the use
of this product.
• This device is not intended for continuous monitoring.
• Do not use this device in an explosive atmosphere.
• Do not use this device in an MRI or CT environment.
INACCURATE MEASUREMENTS MAY BE CAUSED BY THE FOLLOWING:
• Autoclaving, ethylene oxide sterilizing, or immersing the
device in liquid
• Signicant levels of dysfunctional hemoglobins (such as
carbonxy- hemoglobin or methemoglobin)
• Intravascular dyes such as indocyanine green or
methylene blue
•
High ambient light — shield the sensor area (with a
surgical towel, or direct sunlight, for example) if necessary
• Excessive user movement
• High-frequency electrosurgical interference
• Venous pulsations
• Placement of a sensor on an extremity with a blood
pressure cuff, arterial catheter, or intravascular line
• User hypotension, severe vasoconstriction, severe
anemia, or hypothermia
• User cardiac arrest or shock
•
Improper nger placement, e.g. ngernail not facing upward
• Fingernail polish or false ngernails.
SAFETY — PRECAUTIONS FOR USE
WARNING: Indicates a potential hazard situation or
unsafe practice that, if not avoided, could result in death
or serious injury. WARNING statements follow:
Before use, carefully read the manual.
The pulse oximeter has no alarms. Do not use the pulse
oximeter in situations where alarms are required. It is not
for continuous monitoring.
The pulse oximeter is intended only as an adjunct in user
assessment. It must be used in conjunction with other
methods of assessing clinical signs and symptoms.
CAUTION: Indicates a potential hazard or unsafe
practice that, if not avoided, could result in moderate or
minor personal injury. CAUTION statements follow:
Check the pulse oximeter sensor application site
frequently to determine the positioning of the sensor and
circulation and skin sensitivity of the user.
Do not stretch the adhesive tape while applying the pulse
oximeter sensor. This may cause inaccurate readings or
skin blisters.
Prolonged use or the user’s condition may require
changing the sensor site periodically. Change sensor site
and check skin integrity, circulatory status, and correct
alignment at least every 4 hours.
s NOTICE: Indicates a potential hazard or unsafe practice
that, if not avoided, could result in product/property
damage.
SETUP
Battery Installation
1. Open battery compartment cover.
2.
Install two AAA batteries in battery
compartment, ensuring polarities are correct.
3. Close battery compartment cover: Push cover horizontally
along the arrow as shown at right.
s NOTICE:
• Ensure battery polarities are correct, or the device could
be damaged.
Lanyard Installation
1.
Thread the thinner end of the lanyard through the oximeter
loop.
2. Thread the thicker end of the lanyard through the threaded
end, then pull it tightly.
OPERATION INSTRUCTIONS
1. Use isopropyl alcohol to clean the test nger and the rubber
inside the oximeter that touches the nger.
2. Place clamp over ngernail as shown
at right; insert nger, ngernail up as
shown.
3. Press button on front panel once. User’s nger and body
must remain still during measurement.
4. See display: the SpO2 value automatically displays, the
pulse bar graph displays the pulse rate, and the bar graph’s
height shows the pulse strength.
MAINTENANCE AND STORAGE
s NOTICE:
• This device contains no serviceable parts. Do not
disassemble.
• Remove the batteries if the oximeter will not be used for a
long period of time.
• Do not autoclave, sterilize with ethylene oxide, or
immerse the device in liquid.
• See SPECIFICATIONS/Environmental Requirements for
operation and storage requirements. A wet ambience
could damage this product and shorten its lifetime.
• Recycle or dispose of this device and its used batteries in
observance of local regulations.
Info: Use isopropyl alcohol to clean the rubber (inside
the oximeter, that touches the nger) and the test nger
before and after each test. The rubber inside the oximeter
is medical rubber, which has no toxins, and is not harmful
to the skin.
•
Replace the batteries when low battery indicator illuminates.
2
SPECIFICATIONS
Display Type LED (Light Emitting Diode)
SpO2Measurement
range
70-99%
Accuracy 80%-99%: ±2%
70%-79%: ±3%
≤69% : no denition
Pulse Rate Measurement
range
30-235 BPM
Accuracy 30~99 BPM: ±2 BPM
100~235 BPM: ±2%
Pulse Intensity Bargraph Indicator
Power Requirement Two AAA alkaline Batteries
Power Consumption <40 mA
Low Power Indicator
Battery Life ~ 30 hours of continuous operation
Dimension
(L x W x H)
2.20″ ~ 2.44″ x 1.26″ ~ 1.50″ x 1.34″ ~ 1.50″
(56 mm ~ 62 mm x 32 mm ~ 38 mm x 34 mm ~ 38 mm)
Weight 1.59 oz ~ 2.12 oz (0.10 lb ~ 0.13 lb) (45 g ~ 60 g)
including two AAA batteries
Environmental
Requirements
Temperature Operation 41°F ~ 104°F
(5°C ~ 40°C)
Storage 68°F ~ 131°F
(20°C ~ 55°C)
Humidity
(non-condensing)
Operation ≤80% RH
Storage ≤93% RH
Interference
Resistance Capacity
against Ambient Light
Device works normally when mixed noise produced
by BIO-TEK INDEX Pulse Oximeter tester
DECLARATION
This product’s EMC complies with IEC60601-1-2 standard.
The materials with which the user can come into contact have
no toxicity, no action on tissues, and 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 specied 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 emission
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.
TROUBLESHOOTING
Problem Possible reason Solution
SpO2 or PR
cannot be
displayed
normally
1. User's nger is incorrectly
inserted
2. User’s Oxyhemoglobin
value is too low to be
measured
1. Reinsert user's nger
2.
Attempt several times to
obtain a reading; If sure that
no problem exists, obtain
further clinical examination
SpO2 or PR
display is
unstable
1. Finger may not be
inserted deeply enough
2. Finger trembling or user
moving
1. Reinsert nger
2. Ask user to remain still
Troubleshooting continued
Problem Possible reason Solution
Oximeter
cannot be
powered on
1. Battery power may be
inadequate or batteries
may not be installed
2. Batteries may be installed
incorrectly
3.
Oximeter may be damaged
1. Replace batteries
2. Reinstall batteries
3. Contact GF distributor
Indicator
lamps are
suddenly
off
1. Device automatically
powers off when no signal
is detected for longer than
8 seconds
2. Batteries too weak to
power device
1. Normal
2. Replace the batteries
“Error3” or
“Error4”
displays
1. Low power
2. Receiving tube and/or
connector may be
shielded or damaged
3. Mechanical misplace for
receive-emission tube
4. Amp circuit malfunction
1. Replace batteries
2. Contact GF distributor
3. Contact GF distributor
4. Contact GF distributor
“Error7”
displays
1. Low power
2. Emission diode damaged
3. Current control circuit
malfunction
1. Replace batteries
2. Contact GF distributor
3. Contact GF distributor
SYMBOL DEFINITIONS
Symbol Denition Symbol Denition
Type BF applied part Low power indicator
Attention, consult
accompanying documents
No SpO2 Alarm
﹪ SpO2Oxygen saturation Power switch
❤
BPM Heart rate (BPM) SN Serial Number
Info: The illustration used in this manual may differ slightly
from the appearance of the actual product.
LIMITED WARRANTY
GF Health Products, Inc. warrants the John Bunn® JB0217
OxyRead Fingertip Pulse Oximeter to be free from defects in
workmanship and materials for one year.
The warranty does not apply to damage resulting from failure to
follow the operating instructions, accidents, abuse, alterations or
disassembly by unauthorized individuals.
If a product is deemed to be under warranty, GF Health Products,
Inc. shall provide, at its option, (1) replacement of any defective
part or product or (2) a credit of the original selling price made to
GF Health Products, Inc.’s initial customer. The warranty does
not include any labor charges incurred in replacement part(s)
installation or any associated freight or shipping charges to GF
Health Products, Inc.
The warranties contained herein contain all the representations
and warranties with respect to the subject matter of this
document, and supersede all prior negotiations, agreements and
understandings with respect thereto. The recipient of this document
hereby acknowledges and represents that it has not relied on any
representation, assertion, guarantee, warranty, collateral contract
or other assurance, except those set out in this document.
www.grahamfield.com
GF Health Products, Inc. is not responsible for typographical errors. All illustrations,
specications, packaging and warranties contained in this literature are based on the
latest product information available at the time of printing. The most current product
information, including the most current version of these instructions, can be found online at
www.grahameld.com.
Graham-Field and John Bunn are registered trademarks of GF Health Products, Inc.
© 2012 GF Health Products, Inc., Atlanta GA 30360, 770-368-4700 JB02017-INS-LAB-RevB12
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