Kinetik Wellbeing JPD500E Instruction manual

Pulse Oximeter JPD-500E

Instructions to User

Thank you for purchasing the Pulse Oximeter.
This Manual is written and compiled in accordance with the council directive
MDD 93/42/EEC for medical devices and harmonized standards. In case of
modifications and software upgrades, the information contained in this
document is subject to change without notice.
Please read the User Manual carefully before using this product.

WARNING:

■ Discomfort or pain may occur if using the device for long periods of time,
especially for microcirculation barrier patients. It is recommended that the
sensor is not applied to the same finger for over 2 hours.

■ The light (infrared is invisible) emitted from the device is harmful to the

eyes, so the user and all maintenance should not stare at the light.

■ Enamel or acrylic nail polish or other nail applications may distort and/or

produce inaccurate readings.

■ Please refer to the correlative literature about any clinical restrictions or

cautions.

■ This device is not intended for treatment.

1 Safety

1.1 Instructions for Safe Operation

■ Check the main unit and all accessories periodically to make sure that
there is no visible damage that may affect patient’s safety and monitoring
performance about cable and transducers. It is recommended that the
device is inspected once a week at least. When there is obvious damage,
stop using the monitor.

■ Necessary maintenance must be performed by qualified service
engineers ONLY. Users are not permitted to maintain it by themselves.

■ The oximeter cannot be used together with devices not specified in the

User Manual. Only accessories appointed or recommended by the
manufacture can be used with this device.

■ This product is calibrated before leaving factory.

1.2 Warnings

■ Explosive hazard: DO NOT use the oximeter in an environment with

inflammable gas such as ignitable anaesthetic agents.

■ DO NOT use the oximeter if the user is being measured by an MRI or

CT scan.

■ DO NOT use the device if allergic to rubber.

■

The disposal of scrap material, the device’s accessories and packaging

(including batteries, plastic, foam and paper) should follow th

and regulations.

■ Please check the pack’s contents before use to make sure the device

and accessories are in accordance with the packing list, otherwise the
device may work abnormally.

1.3 Attentions

● Keep the oximeter away from dust, vibration, corrosive substances,
explosive materials, high temperature and moisture.

● If the oximeter gets wet, stop operation.

● If the device is moved from a cold environment to a warm or humid

environment, please do not use it immediately.

● High temperature or high pressure steam disinfection of the oximeter is
not permitted. Refer to section 7 of the User Manual for instructions on

cleaning and disinfection.

● Do not immerge the oximeter in liquid. To clean, wipe its surface with
alcoholic wipes. Do not spray any liquid on the device directly.

● Do not use the device on small children and babies.

● The product is suitable for 4+ years old and for those who weigh

between 15kg – 110kg.

e local laws

● The device may not work for all patients. If you are unable to achieve stable

readings, discontinue use.

● The update period of data is less than 5 seconds, which may change
according to the individual’s pulse rate.

● The device has a normal lifespan of five years since the first electrified use.

● The device shows low-voltage but does not have a low-voltage alarm

function. Please change the battery when the battery dies.

● Batteries must be removed if the device is going to be stored for more than a

month in case batteries leak.

1.4 Indication for use

The Finger Pulse Oximeter is a non-invasive device intended for the spot-check

of oxygen saturation of arterial haemoglobin (SpO2) and the pulse rate of adult
and paediatric patients in home and hospital environments (including clinical
use in internist/surgery, anaesthesia, intensive care etc.) This device is not

intended for continuous monitoring.

2 Overview

The pulse oxygen saturation is the percentage of HbO2 in the total Hb in the
blood, also known as the O2 concentration in the blood. It is an important

bio-parameter for respiration. For the purpose of measuring the SpO2 more

easily and accurately, our company developed the Finger Pulse Oximeter. The
device can also measure pulse rate simultaneously.
The Pulse Oximeter features a convenient operation, low power consumption,
small size and portability.
small volume, low power consumption, convenient operation and portability. A
patient needs to put just one finger onto the photoelectric sensor for diagnosis,
and a display screen will directly show the measured value of Haemoglobin

Saturation.

2.1 Classification:

Class II b (MDD 93/42/EEC IX Rule 10)

2.2 Features

■ Simple and convenient operation

■

Small size, lightweight and portable (total weight is 50g est. including

batteries)

■ Low power consumption

■ The product will automatically turn off when out of use for over 16 seconds

2.3 Major Applications and Scope of Application

The Pulse Oximeter can be used to measure Haemoglobin Saturation
pulse rate through the finger, and indicate the pulse intensity by the bar-display.
The product is suitable for use at home, in hospital, oxygen bar, social medical
organisations and to measure oxygen saturation and pulse rate.
The product is not suitable for continuous supervision of patients.

The product is not suitable for use in continuous supervision for patients.

2.4 Environment Requirements

Operation Temperature: 5ºC-40ºC

Storage Temperature: -10ºC-50ºC
Ambient Humidity: 15%-80% RH, no condensation in operation

Atmospheric Pressure: 70 kPa to 106 kPa, in operation

3 Principle and Caution

3.1 Principle of Measurement

Principle of Oximeter: An experienced formula of data processing is established

using Lambert Beer Law according to Spectrum Absorption Characteristics of
Reductive Haemoglobin (Hb) and Oxyhaemoglobin (HbO2) in glow &

near-infrared zones.

10%-93% RH, no condensation in storage

50kPa–106 kPa, in storage

and

Operation of Oximeter: Photoelectric Oxyhaemoglobin inspection

Technology is adopted in accordance with Capacity Pulse Scanning &
Recording Technology, so that two beams of different wavelength of lights

can be focused onto the fingertip through a perspective clamp finger-type
sensor. The measured signal can be obtained by a photosensitive element,

information acquired through which will be shown on screen through

treatment in electronic circuits and a microprocessor.

Figure 1 Operating principle

3.2 Caution

1. Place the finger properly (see Figure 5) to avoid inaccurate
measurement.

2. The SpO2 sensor and photoelectric receiving tube should be arranged

with the subject’s arteriole in between.

3. Excessive ambient light may affect the measuring result. This includes
fluorescent lamps, dual ruby lights, infrared heaters direct sunlight and etc.

4. Strenuous action or extreme electrosurgical interference may also affect

the accuracy.

4 Accessories

■ 1 x Lanyard

■ 2 x AAA Batteries

■ 1 x User Manual.

5 Installation

5.1 View of the Front panel

Figu

5.2 Battery

Step 1. Refer to Figure 3. and insert the two AAA in the correct direction.
Step 2. Replace the cover.

Please take care when you insert the batteries as improper
insertion may damage the device.

Figure 3. Batteries Installation

5.3 Attaching the Lanyard

Step 1. Put one end of the lanyard through the hole.
Step 2. Put the other end of the lanyard through the first one and tighten.

re 2. Front View

The display is

1. The device will power off

drained.

1. Normal.

Description

%SpO2

The pulse oxygen saturation (%)

Pulse rate (bpm)

The battery voltage indication is deficient (change the
battery in time avoiding the inexact measure)

1. No finger inserted

2. An indicator of signal inadequacy

IP22

Ingress of liquids rank

Display Mode

Display Format

LED display

The Pulse Oxygen

Digital
Pulse Intensity (bar-graph)

Digital bar-graph display

SpO2 Parameter Specification

Measuring range

35%-100% (the resolution is 1%).

Accuracy

70%-100%;±2%, Below 70% unspecified.

Pulse Parameter Specification

Measuring range

25bpm-250bpm (the resolution is 1 bpm)

Accuracy

±2bpm

Pulse Intensity

Range

Continuous bar-graph display, the higher

Alert conditions

SpO2

Less than 94%

PR

Less than 50bpm or more than 130bpm

Battery Requirement

2 X 1.5V (AAA size) alkaline battery

Power Consumption

Smaller than 35 mA.

Battery Useful Life

Two batteries can work continually for 24 hours

Power off

The oximeter will switch off if there is no activity for 16 seconds.

Optical Sensor

Red light (wavelength is 660nm)

Dimensions and Weight

Dimensions

62 (L)X37 (W)X32(H) mm

Weight

About 50g (with the batteries)

Guidance and manufacture’s declaration – electromagnetic emission

The JPD-500E is intended for use in the electromagnetic environment

Emission
test

Compliance

Electromagnetic environment –
guidance

The JPD-500E uses RF energy only for its

equipment.

The JPD-500E is suitable for use in all

for domestic purposes.

Display Information

Symbol

Figure 4. Attaching the Lanyard

6 Operating Guide

6.1 Insert the two batteries properly to the direction, and the

cover.

6.2 Open the clip as shown in Figure 5.

n replace the

off suddenly

9 Key of Symbols

Type BF applied part

Warning, see User manual.

automatically when there is
no signal within 16 seconds.

2. The batteries are almost

2. Change batteries.
Infrared (wavelength is 905nm)

11 Appendix: Electromagnetism Compatibility

Guidance and manufacture’s declaration – electromagnetic
emissions-for all EQUIPMENT and SYSTEMS

Figure 5. Put finger in position

6.3 Place finger into the clip with the fingertip over the sensor, and then clip

the finger.

6.4 Press the button once on the front panel.

6.5 Do not shake the finger and remain still during the process.

6.6 Read the information on the screen display.

6.7 In boot-strap state press the button and the device will reset.

Fingernails and the luminescent tube should be on the same side.

7 Repairing and Maintenance & cleaning and disinfection

■ Change the batteries when the low-voltage displays on the screen.

■ Clean the surface of the device with a medical alcoholic wipe before

using. Allow it to air dry in air or dry with a clean fabric first.

■ Use a medical alcoholic wipe to disinfect the product after use to
prevent cross infection in future use.

■ Please take out the batteries if the oximeter is not in use for a long time.
W

arning: High-pressure sterilization cannot be used on the de
Warning: Do not immerse the device in liquid.
Warning: It is recommended that the device should be kept in a dry
environment. Humidity may reduce the device’s lifespan, or even damage it.

8 Troubleshooting

Trouble Possible Reason Solution

The SpO2 and
Pulse Rate

can not be
displayed
normally

The SpO2 and
Pulse Rate

are not
displayed
stably

The device
can not be
turned on

1. The finger is not properly
positioned.

2. The patient’s SpO2 is too

low to be detected.

1. The finger is not placed
inside deep enough.

2. The finger is shaking or
the patient is moving.

1. Low battery or no battery.

2. The batteries are not
inserted properly.

3. The malfunction of the
device.

1. Place the finger
properly and try again.

2. Try again; Go to a
hospital for a diagnosis
if you are sure the
device works all right.

1. Place the finger
properly and try again.

2. Let the patient keep

calm

1. Change batteries.

2. Reinstall batteries.

3. Please contact the
local service center.

vice.

When end users abandon this product, they must send the
product to the collection place for recycling.

10 Technical Specification

Saturation (SpO2)

Pulse Rate (PR) Digital

display indicates the stronger pulse.

specified below. The customer of the user of the JPD-500E should assure
that it is used in such and environment.

RF
emissions
CISPR 11

RF
emission
CISPR 11

Warranty

Your product is warranted to be free of defects in materials and workmanship
for one year from the original purchase date. The device was built to
exacting standards and carefully inspected prior to shipment. In the event of
a defect covered by this warranty there is the option to repair or replace the
device. This warranty does not cover device failure due to owner misuse or
negligence, or normal wear and tear. If you have questions about your
device or the warranty, ple

Group 1

Class B

internal function. Therefore, its RF
emissions are very low and are not likely to
cause any interference in nearby electronic

establishments, including domestic
establishments and those directly
connected to the public low-voltage power
supply network that supplies buildings used

ase contact the local distributor.

0482

WellKang Ltd
Suite B, 29 Harley Street, London W1G 9QR, UK

Shenzhen Jumper Medical Equipment Co., Ltd

Address: Building D, No. 71, Xintian Road, Fuyong Street,
Baoan, Shenzhen, Guangdong, P. R. China, 518103

KINETIK JPD-500E UK IB 20181231