Graham Field oxycheck jb02017 사용자 설명서

OXYCHECK

FINGERTIP

PULSE OXIMETER

MODEL JB02017

OPERATOR MANUAL

GENERAL DESCRIPTION

The John Bunn

JB02017 OxyCheck 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

)

value, pulse rate value, and pulse strength. When a finger is

inserted into the sensor’s rubber cushion, the SpO

value auto-

matically 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 finger-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.

Red and Infrared Emission Tube

Red and Infrared Receipt Tube

INTENDED USE

The intended use of the OxyCheck Fingertip Pulse Oximeter is

the measurement and display of the functional oxygen satura-

tion of arterial hemoglobin (SpO

) and pulse rate (PR) of adults

and pediatric users in hospital, ambulatory, home, and EMS

(Emergency Medical Service) environments. The Pulse Oxim-

eter 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

• Significant levels of dysfunctional hemoglobins (such as

carbonxy- hemoglobin or methemoglobin)

• Intravascular dyes such as indocyanine green or methy-

lene blue

• High ambient light — shield the sensor area (with a surgi-

cal 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 pres-

sure cuff, arterial catheter, or intravascular line

• User hypotension, severe vasoconstriction, severe ane-

mia, or hypothermia

• User cardiac arrest or shock

• Improper finger placement, e.g. fingernail not facing upward

• Fingernail polish or false fingernails.

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 prac-

tice that, if not avoided, could result in moderate or

minor personal injury. CAUTION statements follow:

Check the pulse oximeter sensor application site frequent-

ly to determine the positioning of the sensor and circula-

tion 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 chang-

ing the sensor site periodically. Change sensor site and

check skin integrity, circulatory status, and correct align-

ment 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 compart-

ment, ensuring that polarities are correct.

3. Close battery compartment cover: Push cover horizontally

along the arrow as shown at right.

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 finger and the rubber

inside the oximeter that touches the finger.

2. Place clamp over fingernail as shown

at right; insert finger,

fingernail up as

shown.

3. Press button on front panel once.

User’s finger and body

must remain still during measurement.

4. See display: the SpO

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 disas-

semble.

• Remove the batteries if the oximeter will not be used for a

long period of time.

• Do not autoclave, sterilize with ethylene oxide, or im-

merse 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 finger) and the test finger before

and after each test. The rubber inside the oximeter is medi-

cal rubber, which has no toxins, and is not harmful to the

skin.

• Replace the batteries when low battery indicator illuminates.