Guangdong Healthtree Medical Technology JKS50A Fingertip Pulse Oximeter Owner’s Manual

June 5, 2024
Guangdong Healthtree Medical Technology

Guangdong Healthtree Medical Technology JKS50A Fingertip Pulse Oximeter Owner’s Manual

General Description

The measurement of oxygen saturation of arterial blood (also known as pulse oxygen saturation, usually shortened as SpO2) adopts the principles of light spectra and volume tracing. The LED emits lights with two specific wavelengths, which are selectively absorbed by oxygenated hemoglobin and deoxyhemoglobin. The optical receptor measures the changes in the light intensity after the light passes the capillary network and estimates the ratio of oxygenated hemoglobin and the total hemoglobin.
Instruction

  1. Indication of screen brightness
  2. Indication of pulse intensity
  3. SpO2 Plethysmogram
  4. Indication of battery capacity
  5. Pulse rate reading
  6. SpO2 reading
  7. PI reading
    Product Description

Precautions for use

  • Explosion hazard. Do not use the oximeter in the presence of flammable anesthetics mixture with air, oxygen, or hydrogen.

  • When the oximeter is in use, there should not be any great power appliances as high voltage cables, X-ray machine, ultrasound equipment and electrizer in use nearby.

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

  • This oximeter for sports or aviation use only.

  • The oximeter should be handled with care so as to avoid shocks and falls.

  • When the oximeter is in use, it must be ensured the batteries have sufficient capacity; otherwise there might be such phenomena as starting-up abnormalities or inaccurate measurement data, etc.

  • Please do not use such pointed objects as pen point or nails for pressing operation, otherwise it might cause permanent damage to the surface of the keyboard.

  • To ensure accurate performance and prevent device failure, do not expose the oximeter to extreme moisture, such as direct exposure to rain. Such exposure may cause inaccurate performance or device failure.

  • Do not conduct SpO2 measurement on the finger smeared with nail polish, otherwise this will lead to unreliable measurement results.

  • Please do not open the enclosure. The enclosure shall only be opened by the authorized person.

  • In order to have more accurate measurements of SpO2 and PR, the
    oximeter should be used in quiet and comfortable environment.

  • Follow local ordinances and recycling instructions regarding disposal or recycling of the device and device components, including batteries.

Intended Use

This product is intended for sports and aviation use only. It should not be used to diagnose or treat any medical condition.

Operation Instructions

  1. Install two AAA batteries into battery cassette before closing its cover.
  2. Nip the oximeter, then insert one of fingers into the rubber hole of the oximeter before releasing the oximeter, and your nail surface must be upward.
  3. Press the function button once on front panel.
  4. Your finger and body do not tremble during measuring.
  5. Read corresponding data in only one direction on the display screen.

Battery Installations

Battery Installations

  1. Press the button down on the back panel of oximeter and push the battery cover horizontally along the arrow shown as below:
  2. Install the two AAA batteries into battery cabin in correct polarities.
  3. Close the battery cover.

Notes:

  • Pay attention to the correct polarities terminals of the battery, which are marked with plus and minus signs. Do not install the battery in the direction of the spring.
  • Please remove the battery if the oximeter will not be used for long time.

Maintenance

  1. Use a soft cloth dampened with either a commercial, nonabrasive cleaner, or a solution of 70% alcohol in water, lightly wipe the surfaces of the oximeter.
  2. The most commonly used hospital cleaning agent and non-corrosive detergents can be used for cleaning the oximeter, but please be careful that many types of detergents must be diluted before use; Please use them according to the directions of the manufacturers of the detergents.
  3. Avoid using alcohol-based, amido or acetone-based detergents
  4. The casing of the oximeter should be kept from the contamination of filth and dirt, and it can be wiped with non-velvet soft cloth. When cleaning, do not spill the liquid onto the instrument. Ensure no liquid is allowed to enter the inside of the oximeter.
  5. It is forbidden to use such grinding materials as wire brush or metal polishing agent, because these materials may cause damage to the panels of the oximeter.
  6. Please do not soak the oximeter in liquid.
  7. Under normal circumstances, it is unnecessary for the oximeter to have special maintenance, and cautions must be exercised on the following points during the use of the oximeter:
    • Please use the oximeter in the environment according to the requirements of the performance criteria.
    • Avoid contacts with organic solutions, dusts or corrosive gases.

Product Specifications

Measurement specifications

SpO 2

Measuring Range| 0~100%
Resolution| 1%
Accuracy| At 70~100%, ±2%At 0~69%, unspecified
Data update period| <13 s
PR
Measuring Range| 25~250 bpm
Resolution| 1 bpm
Accuracy| ±1% or ± 1 bpm, whichever is greater
Data update period| < 13 s

Battery specifications

Type Voltage
two AAA alkaline battery 1.5 Volts DC (per battery)

The oximeter uses two 1.5 V A AA type batteries and a set of new batteries can be used for more than 18 hours, depending on concrete battery types.

Environmental specifications

Operation

Temperature +5℃~+40℃
Atmospheric Pressure 700hPa~1060hPa
Relative Humidity ≤85%

Transport and Storage

Temperature -20℃~+55℃
Atmospheric Pressure 500hPa~1060hPa
Relative Humidity ≤93%

Physical specifications

Weight about 21g (exclude battery) about 54g (include battery)
Dimensions 57mm(length) × 33mm(width) ×30mm(height)

Sensors specifications

Wavelength| Pulse oximetry sensors contain LEDs that emit red light at a wavelength of approximately 660 nm and infrared light at a wavelength of approximately 905 nm.
The total optical output power of the sensor LEDs is less than 15 mW.
This information may be useful to clinicians, such as those performing photodynamic therapy.
Note: Sensor LED light emissions fall within Class 1 level, according to IEC 60825-1:2001. No special safety precautions are required.
---|---

Possible Problems and resolutions

Problems

| Possible causes|

Solution

---|---|---
There is no response to the function button.| The button can not be pressed to its position| Ensure that the button is fully depressed.
Battery capacities are low| The batteries may be missing, discharged, or oriented incorrectly.
Replaced them with new ones.
The Pulse search time is too long| Perfusion may be too low| Change the measuring site. Try another oximeter.
person movement| Interference due to person activity may be preventing the oximeter from tracking the pulse. Keep the person still, if possible.
Electromagnetic interference may be preventing the oximeter from tracking the pulse.| Remove the source of interference.
There may be interference due to ambient light, or the oximeter may be on an extremity with a blood pressure cuff, arterial catheter, or intravascular line.| Reposition oximeter, as necessary.
Display is dark-or-bright| Battery capacities are low.| Replace the batteries.

Symbols Definitions

Symbol

|

Definition

---|---
| Type BF equipment (Refer to IEC 60601-1:1995)
| Attention! Please refer to this manual.

%SpO 2

| Oxygen saturation of arterial blood

/Min

| Pulse rate
| Non-Alarm indication (The device does not have alarm function)

IPX1

| Enclosure degree of ingress protection.

SN

| Serial number
| Symbol for the marking of electrical and electronics devices according to Directive 2002/96/EC.
The device, accessories and the packaging have to be disposed of waste correctly at the end of the usage. Please follow Local Ordinances or Regulations for disposal.
Note: The Oximeter is applied to this regulation.

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

Guidance and manufacture’s declaration – electromagnetic emission

The Fingertip Pulse Oximeter is intended for use in the electromagnetic environment specified below. The customer of the user of the Fingertip Pulse Oximeter should assure that it is used in such and environment.
Emission test| Compliance| Electromagnetic environment – guidance
RF emissions CISPR 11| Group 1| The Fingertip 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 Fingertip 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.

Applicable Models

JKS50B

Packing List

NO.

| Item| Quantity
---|---|---
1| Oximeter| 1|

2

| AAA battery| 2|
3| Cord| 1|

4

| User’s manual| 1|

Guangdong HealthTree Medical Technology Co., Ltd.

ADD: 710, Area B, Dazhou Science and Technology Park, Xiangzhou
District, Zhuhai City,Guangdong Province,China
Tel: +86-13631235424
E-mail: 1152061380@qq.com
Website: www.healthtreeltd.com

FCC Caution

§ 15.19 Labelling requirements.

This device complies with part 15 of the FCC Rules. Operation is subject to the following two conditions: (1) This device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation.

§ 15.21 Information to user.

Any Changes or modifications not expressly approved by the party responsible for compliance could void the user’s authority to operate the equipment.

§ 15.105 Information to the user.

Note: This equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential installation. This equipment generates uses and can radiate radio frequency energy and, if not installed and used in accordance with the instructions, may cause harmful interference to radio communications. However, there is no guarantee that interference will not occur in a particular installation. If this equipment does cause harmful interference to radio or television reception, which can be determined by turning the equipment off and on, the user is encouraged to try to correct the interference by one or more of the following measures:

  • Reorient or relocate the receiving antenna.
  • Increase the separation between the equipment and receiver.
  • Connect the equipment into an outlet on a circuit different from that to which the receiver is connected.
  • Consult the dealer or an experienced radio/TV technician for help.

References

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