background image

PULSE OXIMETER

GENERAL DESCRIPTION

FRONT PANEL

BATTERY INSTALLATION

USING THE LANYARD

MAINTENANCE AND STORAGE

SPECIFICATIONS

MEASUREMENT PRINCIPLE

PRECAUTIONS FOR USE

CONTRAINDICATION

INACCURATE MEASUREMENTS MAY BE CAUSED BY

PRODUCT FEATURES

INTENDED USE

OPERATION INSTRUCTIONS

Oxygen Saturation is a percentage of Oxyhemoglobin (HbO2) capacity, compounded with oxygen, by all combinative hemoglobin (Hb) 

capacity in blood. In other words, it is consistency of Oxyhemoglobin in blood. It is a very important parameter for the Respiratory 

Circulation System. Many respiratory diseases can result in oxygen saturation being lowered in human blood. Additionally, the following 

factors can reduce oxygen saturation: Automatic regulation of organ dysfunction caused by Anesthesia, Intensive Postoperative Trauma, 

injuries caused by some medical examinations. That situation might result in light-headedness, asthenia, and vomiting. Therefore, it is 

very important to know the oxygen saturation of a patient so that doctors can find problems in a timely manner. 

The fingertip pulse oximeter features low power consumption, convenient operation and portability. Place one fingertip into the 

photoelectric sensor for diagnosis and the pulse rate and oxygen saturation will appear on the display. It has been proven in clinical 

experiments that it also features high precision and repeatability.

Principle of the oximeter is as follows: A mathematical formula is established making use of Lambert Beer Law according to Spectrum 

Absorption Characteristics of Reductive hemoglobin (RHb) and Oxyhemoglobin (HbO2) in red and near-infrared zones. Operation 

principle of the instrument: Photoelectric Oxyhemoglobin Inspection Technology is adopted in accordance with Capacity Pulse Scanning 

and Recording Technology, so that two beams of different wavelength of lights (660nm red and 905nm near infrared light) can be 

focused onto a human nail tip through a clamping finger-type sensor. A measured signal obtained by a photosensitive element, will be 

shown on the oximeter’s display through process in electronic circuits and microprocessor. 

Diagram of Operation Principle

1. Red and Infrared-ray Emission Tube 

2. Red and Infrared-ray Receipt Tub

1.    Before use, carefully read the manual. 

2.    Operation of the fingertip pulse oximeter may be affected by the use of an electrosurgical unit (ESU).

3.   The fingertip pulse oximeter must be able to measure the pulse properly to obtain an accurate SpO2 measurement. Verify that 

       nothing is hindering the pulse measurement before relying on the SpO2 measurement.

4.   Do not use the fingertip pulse oximeter in an MRI or CT environment.

5.   Do not use the fingertip pulse oximeter in situations where alarms are required. The device has no alarms. It is not for continuous 

      monitoring. 

6.   Do not use the fingertip pulse oximeter in an explosive atmosphere. 

7.    The fingertip pulse oximeter is intended only as an adjunct in patient assessment. It must be used in conjunction with other methods 

       of assessing clinical signs and symptoms. 

8.   In order to ensure correct sensor alignment and skin integrity, the maximum application time at a single site for our device should be 

      less than half an hour. 

9.   Do not sterilize the device using autoclaving, ethylene oxide sterilizing, or immersing the device in liquid. The device is not intended 

       for sterilization. 

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

      batteries. 

11.  This equipment complies with IEC 60601-1-2:2007 for electromagnetic compatibility for medical electrical equipment and/or 

       systems. However, because of the proliferation of radio-frequency transmitting equipment and other sources of electrical noise in 

      healthcare and other environments, it is possible that high levels of such interference due to close proximity or strength of a source 

       might disrupt the performance of this device. 

12. Portable and mobile RF communications equipment can affect medical electrical equipment.

13. This equipment is not intended for use during patient transport outside the healthcare facility.

14. This equipment should not be used adjacent to or stacked with other equipment.

15.  Do not disassemble, repair or modify the equipment without authority.

16. It may be unsafe to:

      —use accessories, detachable parts and materials not described in the instructions for use 

      —interconnect this equipment with other equipment not described in the instructions for use 

      —disassemble, repair or modify the equipment. 

17. These materials that contact with the patient’s skin contain medical silicone and ABS plastic enclosure all pass the ISO10993-5 Tests 

       for invitro cytotoxicity and ISO10993-10 Tests for irritation and delayed-type hypersensitivity.

Rx only: “Caution: Federal law (USA) restricts this device to sale by or on the order of a licensed practitioner.”

It is not for continuous monitoring.

1.    Significant levels of dysfunctional hemoglobin (such as carbonyl - hemoglobin or methemoglobin).

2.   Intravascular dyes such as indocyanine green or methylene blue.

3.   High ambient light. Shield the sensor area if necessary.

4.   Excessive patient movement.

5.   High-frequency electrosurgical interference and defibrillators.

6.   Venous pulsations.

7.   Placement of a sensor on an extremity with a blood pressure cuff, arterial catheter, or intravascular line.

8.   The patient has hypotension, severe vasoconstriction, severe anemia, or hypothermia.

9.   The patient is in cardiac arrest or is in shock.

10. Fingernail polish or false fingernails.

11.  Weak pulse quality (low perfusion).

12. Low hemoglobin.

1.    Simple to operate and convenient to carry. 

2.   Small volume, light weight and low power consumption. 

3.   OLED display SpO2, PR, and Pulse bar. 

4.   Level 1-10 adjustable brightness. 

5.   6 display modes. 

6.   2pcs AAA-size alkaline batteries; battery-low indicator. 

7.    When no or low signal is detected, the pulse oximeter will power off automatically in 8 seconds.

Fingertip pulse oximeter is a portable non-invasive device intended for spot-checking of oxygen saturation of arterial hemoglobin (SpO2) 

and pulse rate of adult and pediatric patients in hospitals, hospital-type facilities. 

1.    Install two AAA batteries according to the Battery Installation instructions. 

2.   Place one of your fingers into the rubber opening of the pulse oximeter. 

3.   Press the switch button one time on front panel to turn the pulse oximeter on. 

4.   Keep your hands still for the reading. Do not shake your finger during the test. It is recommended that you do not move your body

       while taking a reading. 

5.   Read the data from the display screen. 

6.   Press the button again to toggle between six display modes. 

After turning on the Oximeter, each time you press the power switch, the Oximeter will switch to another display mode. 

There are 6 display modes shown as follows: 

The pulse bar less than 30% indicates signal inadequacy and the displayed SpO2 and pulse rate value is potentially incorrect.

1.     Open the battery door cover shown as the picture. 

2.    Install two AAA batteries into the battery compartment. Match the plus (+) and minus (-) signs in the compartment. If the polarities 

       are not matched, damage may be caused to the oximeter. 

3.    Close the battery door cover.

Note:

¤

      

Please remove the batteries if the pulse oximeter will not be used for long periods of time.

¤

  

   Please replace the battery when the low battery power indicator. 

                                                        

1.     Thread thinner end of the lanyard through the hanging hole.

2.    Thread thicker end of the lanyard through the threaded end before pulling it tightly.

            Warnings! 

¤

     Keep the oximeter away from young children. Small items such as the battery door, battery, and lanyard are choking hazards. 

¤

     Do not hang the lanyard from the device’s electrical wire.

¤

     Please notice that the lanyard which is tied to the oximeter may cause strangulation due to excessive length. 

1.    Replace the batteries in a timely manner 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 if the oximeter is not operated for a long time.

4.    It is best to store the product in -20°C~+55°C and ≤93% humidity.

5.    Keep in a dry place. Extreme moisture may affect oximeter lifetime and may cause damage. 

6.    Dispose of battery properly; follow any applicable local battery disposal laws. 

Cleaning the fingertip pulse oximeter 

Please use medical alcohol to clean the silicone touching the finger inside of oximeter with a soft cloth dampened with 70%isopropyl 

alcohol. Also clean the being tested finger using alcohol before and after each test. 

Do not pour or spray liquids onto the oximeter, and do not allow any liquid to enter any openings in the device. Allow the oximeter to dry 

thoroughly before reuse. 

The fingertip pulse oximeter requires no routine calibration or maintenance other than replacement of batteries. 

The use life of the device is five years when it is used for 15 measurements every day and 10 minutes per one measurement. Stop using 

and contact local service center if one of the following cases occurs: 

     

An error in the Possible Problems and solutions is displayed on screen. 

     The oximeter cannot be powered on in any case and not the reasons of battery. 

     There is a crack on the oximeter or damage on the display resulting readings cannot be identified; the spring is invalid; or the key is 

       unresponsive or unavailable.

1. Display Type

OLED display 

2. SpO2 

Display range: 0%~99% 

Measurement range: 70%~99% 

Accuracy: 70%~99%: ±3%; 0%~69% no definition 

Resolution: 1% 

Note:

A functional tester cannot be used to assess the accuracy of a pulse oximeter monitor or sensor. Clinical testing is used to establish the 

SpO2 accuracy. The measured arterial hemoglobin saturation value (SpO2) of the sensors is compared to arterial hemoglobin oxygen 

(SaO2) value, determined from blood samples with a laboratory CO-oximeter. The accuracy of the sensors in comparison to the 

CO-oximeter samples measured over the SpO2 range of 70%~100%. Accuracy data is calculated using the root-mean-squared 

(Arms value) for all subjects, per ISO 9919:2005, Medical Electrical Equipment–Particular requirements for the basic safety and essential 

performance of pulse oximeter equipment for medical use. 

A functional tester is used to measure how accurately Fingertip Pulse Oximeter is reproducing the specified calibration curve and the 

PR accuracy. 

The model of functional tester is Index2 FLUKE simulator and the version is 2.1.3.

3. Pulse Rate 

Display range: 0bpm~250bpm 

Measure range: 30bpm~235bpm 

Accuracy: 30bpm~99bpm, ±2bpm; 100bpm~235bpm, ±2%

Resolution: 1bpm 

4. Probe LED Specifications

Wavelength

Radiant Power

RED

660±2nm

1.8mW

IR

940±10nm

2.0mW

NOTE: 

The information about wavelength range can be especially useful to clinicians. 

5. Power Requirements 

Two AAA alkaline Batteries 

Power consumption: Less than 30mA

Battery Life: Two AAA 1.5V, 600mAh alkaline batteries could be continuously operated as long as 30 hours.

HCSM70P

Holding the power switch for longer than one second, will adjust the brightness of the oximeter. There are 10 levels of brightness. 

The default is level four.

Отзывы: