CMS60C user manual
Contents
1. f Exitthe main menu On the main menu interface press the up button or down button in order to move the menu choice bar to Exit then press the menu button to exit the main menu E Real time data transmission a Pleaseconnect the device with computer by the data line which is equipped with the device then double click SpO2 icon to open SpO2 program b The data can be displayed on computer screen in a few seconds c When you unplug the data line from computer there is a dialog box Save data at view appearing on the desktop in which you can input some patient s basic information F Charge There are two kinds of charging methods a Connect the device with computer by data line then the device should be under charging state b Connect the device with power supply by power adaptor then the device should be under charging state c Thefive status of battery power are shown as follows 10 E Power supply by battery only and battery status is full EE Battery status is not full t rA Battery status is draining away Lag Low power alarm indication Please charge the battery the four status above shows Battery is under charging dynamically in turn d When charging the battery in the state of power off the sign of battery status still exists on the screen but it will disappear in about 60 seconds for saving power However the sign will appear again if you press any button power on off excluded at thi2. mobile radios amateur radio AM and FM radio broadcast cannot be predicted theoretically with accuracy To assess the electromagnetic environment due to fixed RF transmitters an electromagnetic site survey should be considered If the measured field strength in the location in which The Pulse Oxvimeter CMS60C is used exceeds the applicable RF compliance level above the Pu se Oximeter CMS60C should be observed to verify normal operation If abnormal performance is observed additional measures may be necessary such as reorienting or relocating the Pulse Oximeter CMS 60 C Over the frequency range 150 KHz to 80 MHz field strengths should be less than 3V m 17 Recommended separation distances between portable and mobile RF communications equipment and the EQUIPMENT or SYSTEM for EQUIPMENT or SYSTEM that not LIFE SUPPORTING Recommended separation distances between The Pulse Qvimeter CAMMS60C is intended for use in the electromagnetic environment in which radiated RF disturbances are controlled The customer or the user of the Pulse Oxzmeter CA4560C can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment transmitters and the Pzse Orimeter CMS60C as recommended below according to the maximum output power of the communications equipment Separation distance according to frequency of transmitter m 80MHz to 800MHz 800MHz to 2 5GHz Rated maximum
3. down button move the menu choice bar to Alarm then press the menu button to enter the alarm setting menu of figure 7 SOO HLM Ni HG Figure 7 Alarm Setting Menu a The highest lowest alarm limit setting Press the up button or down button to choose the parameter to be adjusted then press the menu button again to enter the similar dialog box shown as figure 8 then press the up button or down button to change data Each press of the up button or down button the data will raise or descend for one time accordingly until it gets to the required number then press the menu button for another time to end the setting Mir the alarm function is on the device will provide midium priority alarm signal when the data of SpO or pulse rate is beyond the limit Intermittent alarm will occur and the measurement shows in yellow Medium priority indicating that prompt operator response is required When operating at the beginning the operator inserts his finger and setup the Spo2 ALM HI lower than the current measured value then the machine will start alarm The pulse rate alarm test is the same with the above Figure 8 b The alarm state setting Press the up button or down button move the menu choice bar to Alarm then choose the alarm state on off by pressing the menu button choose on to start the alarm function and choose off to close it for good b Pulsesound indication setting On the main menu interfac
4. foe use in all CISPR 11 establishments including domestic establishments and Harmonic emissions Not applicable those directly connected to the public low voltage power IEC 61000 3 2 supply network that supplies buildings used for domestic Voltage fluctuations Not applicable purposes flicker emission IEC 61000 3 3 Guidance and manufacture s declaration electromagnetic immunity for all EQUIPMENT and SYSTEMS Guidance and manufacture s declaration electromagnetic immunity The Pulse Oximeter CMS60C is intended for use in the electromagnetic environment specified below The customer or the user of ze Pulse Oximeter CMS60C should assure that it is used in such an environment Electromagnetic Immunity test IEC60601 test level Compliance level environment guidance Electrostatic 6KV contact 6KV contact Floors should be wood concrete or discharge ESD IEC 8KV air 8KV air ceramic tile If floor are covered 61000 4 2 with synthetic material the relative humidity should be at least 30 Power frequency 3A m Power frequency magnetic fields 50Hz magnetic field should be at levels characteristic of IEC 61000 4 8 a typical location in a typical commercial or hospital environment 16 Guidance and manufacture s declaration electromagnetic immunity for EQUIPMENT and SYSTEMS that are not LIFE SUPPORTING Guidance and manufacture s declaration electromagnetic immunity The se QOxzmeter CMS60C is intended for us
5. pulsating blood flow of subject is required For a subject with weak pulse due to shock low ambient body temperature major bleeding or use of vascular contracting drug the SpO waveform PLETH will decrease In this case the measurement will be more sensitive to interference B For those with a substantial amount of staining dilution drug such as methylene blue indigo green and acid indigo blue or carbon monoxide hemoglobin COHb or methionine Me Hb or 11 thiosalicylic hemoglobin and some with icterus problem the SpO determination by this monitor may be inaccurate C The drugs like dopamine procaine prilocaine lidocaine and butacaine may also be a major factor blamed for serious error of SpO measure D As the SpO value serves as a reference value for judgement of anemic anoxia and toxic anoxia some patients with serious anemia may also report good SpO measurement 7 Maintain transportation and storage 7 1 Cleaning and Disinfecting Using medical alcohol to disinfect the device nature dry or clean it with clean soft cloth 7 20 Maintain A Please clean and disinfect the device before using according to the User Manual 7 1 B Please recharge the battery when the screen shows 3 C Recharge the battery soon after the over discharge The device should be recharged every six months when it is no regular used It can extend the battery life following this guidance D Please take out the batteries if the ox
6. read the measured value when the waveform on screen is equably and steady going This measured value is optimal value And the waveform at the monment is the standard one A If some abnormal conditions appear on the screen during test process pull out the finger and reinsert to restore normal use A The device has normal useful life for three years since the first electrified use A This device has the function of alarming users can check on this function according to chapter 6 1 as areference A The device has the function of limits alarming when the measured data is beyond the highest or lowest limit the device would start alarming automatically on the premise of the alarming function is on A The device has the function of alarming this function can either be paused or closed for good please check the chapter 6 1 as a reference A The device may not work for all patients If you are unable to achieve stable readings discontinue use 2 Overview The pulse oxygen saturation is the percentage of HbO in the total Hb in the blood so called the O2 concentration in the blood It is an important bio parameter for the respiration A number of diseases relating to respiratory system may cause the decrease of SpO in the blood furthermore some other causes such as the malfunction of human body s self adjustment damages during surgery and the injuries caused by some medical checkup would also lead to the difficulty of oxygen supply in huma
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8. C 0123 CMS60C Pulse Oximeter User Manual CONTEC MEDICAL SYSTEMS CO LTD Instructions to User Dear users thank you very much for purchasing the Pulse Oximeter This Manual is written and compiled in accordance with the council directive MDD93 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 The Manual describes in accordance with the Pulse Oximeter s features and requirements main structure functions specifications correct methods for transportation installation usage operation repair maintenance and storage etc as well as the safety procedures to protect both the user and equipment Refer to the respective chapters for details Please read the User Manual carefully before using this product The User Manual which describes the operating procedures should be followed strictly Failure to follow the User Manual may cause measuring abnormality equipment damage and human injury The manufacturer is NOT responsible for the safety reliability and performance issues and any monitoring abnormality human injury and equipment damage due to users negligence of the operation instructions The manufacturer s warranty service does not cover such faults Owing to the forthcoming renovation the specific products you received may not be totally in accordance with the description of this
9. User Manual We would sincerely regret for that This product is medical device which can be used repeatedly WARNING Uncomfortable or painful feeling may appear if using the device ceaselessly especially for the microcirculation barrier patients It is recommended that the sensor should not be applied to the same finger for over 2 hours For the special patients there should be a more prudent inspecting in the placing process The device can not be clipped on the edema and tender tissue The light the infrared is invisible emitted from the device is harmful to the eyes so the user and the maintenance man should not stare at the light 6 Testee can not use enamel or other makeup 6 Testee s fingernail can not be too long Please refer to the correlative literature about the clinical restrictions and caution This device is not intended for treatment The User Manual is published by our company All rights reserved I Contents 2 PODES ucc d ut dE LEM ce MI E Ud MM I UM E 2 2Major applications and scope of application tnnt 2 9EnvItontmetrit Xequitemie Bis ee ee ee eR E A YR RE Rea a SP maple eer RU M ETSI Egi TeaIDr RID LER RR toiin A Marnm DetFOEHdliee dam tA etaed M esed aae Ds POA Ce BVM DOR Ier 5 acit tee setinteie te ae crete ct cen Aer dos eve hereto e ee LE Tins Call AEN OM PIPER RR T 5
10. be changed G A pulse sound indication H With alarm function I With SpO value and pulse rate value of storage the stored data can be uploaded to computers J Itcan be connected with an external oximeter probe K Real time data can be transmitted to computers 4 0 Main Parameters A Measurement of SpO Measuring range 0 100 Accuracy When the SpO measuring range is 7096 100 the permission of absolute error is 2226 below 70 unspecified B Measurement of pulse rate Measuring range 30bpm 250bpm Accuracy 2 bpm or 2 select larger C Resolution SpO 1 Pulse rate 16002 D Measurement Performance in Weak Filling Condition SpO and pulse rate can be shown correctly when pulse filling ratio is 0 4 SpO error is 4 pulse rate error is 2 bpm or 2 select larger E Resistance to surrounding light The deviation between the value measured in the condition of man made light or indoor natural light and that of darkroom is less than 1 F Powersupply requirement 3 6 V DC 4 2V DC G Optical Sensor Red light wavelength is 660nm 6 65mW Infrared wavelength is 880nm 6 75mW H Adjustable alarm range SpO s 0 100 Pulse Rate Obpm 254bpm 5 Installation 5 1 View of the front panel pulse sound indication alarm indication SpOz pulse rate battery status indication alarm pulse button up button pulse bar graph menu button power on off button pulse wavefo
11. e in the electromagnetic environment specified below The customer or the user of the Pulse Orimeter CMS60C should assure that it is used in such an environment IEC60601 Compliance Immunity test Electromagnetic environment guidance test level level Portable and mobile RF communication equipment should be used no closer to any part of the Pulse Oximeter CMS600 including cables than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter recommended separation distance Conducted RF 3Vims j 5 IEC 61000 4 6 150kHZ to d EL 80MHZ d ET 80MHz to 800MHz 1 Radiated RF d ZW 800MHz to 2 5GHz IEC 61000 4 3 i Where is the maximum output power rating of the transmitter in watts W according to the transmitter manufacturer and 2 is the recommended separation distance in meters m Field strengths from fixed RF transmitters as determined by an electromagnetic site survey should be less than the compliance level in each frequency range Interference may occur in the vicinity of equipment marked wit the following symbol Co NOTE1 At 80MHz and 800MHz the higher frequency range applies NOTE 2 These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people Field strengths from fixed transmitters such as base stations for radio cellular cordless telephones and land
12. e press the up button or down button move the menu choice bar to Pulse Sound then choose the pulse sound indication state on off by pressing the menu button press on to start the function and press off to close it c Backlight adjustment On the main menu interface press the up button or down button move the menu choice bar to Brightness then press the menu button to change the number in order to adjust the brightness of screen d Data storage setting This device has the function of 24 hours data storage it has the capability of accurately storing pulse rate and SpO data then transmit the data to computer with the data line for replay and analysis a On the main menu interface press the up button or down button move the menu choice bar to Record then press the menu button again to enter the dialog box of figure 9 if it is in recording state the Stop is displayed on menu if it is not in recording state the Start is displayed on menu b When the Start is displayed on the menu if the memory still have the former data in storage the Do you really want to recover the memory dialog box will be displayed when pressing the menu button then press the up button or down button to choose setting then press the menu button to confirm setting the dialog box will be displayed as figure 10 It needs to set the starting time for data storage by users users can change the setting value by pressing the up button or down bu
13. e read directly from the screen on the measuring interface IN Fingernails and the luminescent tube should be on the same side IN If the alarm function is on the device will provide midium priority alarm signal when probe or finger is out Intermittent alarm will occur and the user interface presents FINGER OUT Medium priority indicating that prompt operator response is required Figure 5 C Actual probe may be different with the probe as figure 5 please accept the actual probe with the device B Change display direction On the measuring interface press the screen change button can change the display direction C Pausealarm a Alarm including the alarm of measure data s going beyond the limits the alarm of low voltage the alarm of probe or finger s out of position b When alarm is on press the alarm pause button can pause the alarm it can renew alarm in about 60s and if pressing the alarm pause button Again with in 60s it can renew alarm c Ifyou want to turn offthe alarm for good you should enter the menu for operation D Menuoperations On the measuring interface press the menu button can enter the menu of figure 6 Users can adjust the setting through the main menu such as alarm pulse sound indication backlight data storage data transmission with the use of data line the specific method is as follows Figure 6 Main Menu Interface a Alarm setting On the main menu interface press the up button or
14. ent a Temperature 40 C 60 C b Relative humidity 5 95 c Atmospheric pressure 500hPa 1060hPa Operating Environment a Temperature 10 C 40 C b Relative Humidity 30 75 c Atmospheric pressure 700hPa 1060hPa 3 Principle Principle of the Oximeter is as follows An experience formula of data process is established taking use of Lambert Beer Law according to Spectrum Absorption Characteristics of Reductive Hemoglobin Hb and Oxyhemoglobin HbO2 in glow amp near infrared zones Operation principle of the device is Photoelectric Oxyhemoglobin Inspection Technology is adopted in accordance with Capacity Pulse Scanning amp Recording Technology so that two beams of different wavelength of lights can be focused onto human nail tip through perspective clamp finger type sensor Then measured signal can be obtained by a photosensitive element information acquired through which will be shown on screen through treatment in electronic circuits and microprocessor Glow and Infrared ay 0 Emission Tube T i NLD Glow and Infrared ray S Heceipt Tube Eb UA AAA Figure 1 4 Technical specifications 4 1 Main performance A SpO value display B Pulse rate value display bar graph display C Pulse waveform display D Low voltage indication low voltage indicator appears before working abnormally which is due to low voltage E The display mode can be changed F Screen brightness can
15. g performance about cables and transducers It is recommended that the device should be inspected once a week at least When there is obvious damage stop using the device lt Necessary maintenance must be performed by qualified service engineers ONLY Users are not permitted to maintain it by themselves lt The oximeter cannot be used together with devices not specified in User s Manual Only the accessory that appointed or recommendatory by manufacture can be used with this device lt This product is calibrated before leaving factory 1 2 Warning Explosive hazard DO NOT use the oximeter in environment with inflammable gas such as some ignitable anesthetic agents DO NOT use the oximeter while the testee measured by MRI and CT The person who is allergic to rubber can not use this device The disposal of scrap instrument and its accessories and packings including battery plastic bags foams and paper boxes should follow the local laws and regulations Please check the packing before use to make sure the device and accessories are totally in accordance with the packing list or else the device may have the possibility of working abnormally Please choose the accessories and probe which are approved or manufactured by the manufacturer or else it may damage the device Please choose the battery chargers which should be ensured compliance with the requirements of IEC 601 1 or else it may damage the dev
16. ice The device can only be matched with the compatible probe Please don t measure this device with functional tester for the device s related information 1 3 Attention A Keep the oximeter away from dust vibration corrosive substances explosive materials high temperature and moisture A fthe oximeter gets wet please stop operating it A When t is carried from cold environment to warm or humid environment please do not use it immediately A DO NOT operate keys on front panel with sharp materials A High temperature or high pressure steam disinfection of the oximeter is not permitted Refer to User Manual in the relative chapter 7 1 for instructions of cleaning and disinfection A Do not have the oximeter immerged in liquid When it needs cleaning please wipe its surface with medical alcohol by soft material Do not spray any liquid on the device directly A When cleaning the device with water the temperature should be lower than 60 C A As to the fingers which are too thin or too cold it would probably affect the normal measure of the patients SpO and pulse rate please clip the thick finger such as thumb and middle finger deeply enought into the probe A The pulse oximeter can be used to adult or infant Whether the device is used to adult or infant it depends on the probe selected A The update period of data is less than 5 seconds which is changeable according to different individual pulse rate A Please
17. imeter is not in use fora long time E The device needs to be calibrated once a year or according to the calibrating program of hospital It also can be performed at the state appointed agent or just contact us for calibration 7 3 Transportation and storage A The packed device can be transported by ordinary conveyance or according to transport contract The device can not be transported mixed with toxic harmful corrosive material B The packed device should be stored in room with no corrosive gases and good ventilation Temperature 40 C 60 C Humidity lt 95 8 Troubleshooting 1 Place the finger properly and The 5002 and Pulse 1 The finger is not properly positioned try again Rate can not be 2 The patient s SpO is too low to be 2 Try again Go to a hospital for displayed normally detected a diagnosis if you are sure the device works all right 1 The fi t placed inside d The SpO and Pulse i ep 1 Place the finger properly and enough Rate are not try again i 2 The finger is shaking or the patient is is display ed stably 2 Let the patient keep calm moving 1 Please recharge the batter 1 The battery is drained away or almost E 2 Please Install the battery The device can not drained away l again be turned on 2 The battery is installed incorrectly 3 Please contact the local service 3 The malfunction of the device center 12 The displa
18. n body and the corresponding symptoms would appear as a consequence such as vertigo impotence vomit etc Serious symptoms might bring danger to human s life Therefore prompt information of patients SpO is of great help for the doctor to discover the potential danger and 1s of great importance in the clinical medical field The Pulse Oximeter features in small volume low power consumption convenient operation and being portable It is only necessary for patients to put one of his fingers into a probe for diagnosis and a display screen will directly show the measured value of pulse oxygen saturation with the high veracity and repetition 2 1 Features A Operation of the product is simple and convenient B The product is small in volume light in weight and convenient in carrying C Low power consumption 2 20 Major applications and scope of application The Pulse Oximeter can be used in measuring the pulse oxygen saturation and pulse rate through finger The product is suitable for being used in family hospital oxygen bar community healthcare physical care in sports It can be used before or after doing sports and it is not recommended to use the device during the process of having sport and etc The problem of overrating would emerge when the patient is suffering from toxicosis which caused by carbon monoxide the device is not recommended to be used under this circumstance 2 3 Environment requirements Storage Environm
19. output power of transmitter 100 11 6667 23 3334 For transmitters rated at a maximum output power not listed above the recommended separation distanced in meters m can be estimated using the equation applicable to the frequency of the transmitter where P is the maximum output power rating of the transmitter in watts W according to the transmitter manufacturer NOTE At 80MHz and 800MHz the separation distance for the higher frequency range applies NOTE2 These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people Appendix 2 Alarm condition delay Alarm signal generation delay Probe error alarm 1 61208 20ms
20. ower h When the storage space is full it displays Memory is full on the screen and then shut down in a few seconds But it will still display Memory is full by the next time you turn on the device on the purpose of warning the user if press any button power on off excluded again it will enter the measuring interface e Stored data transmission setting Firstly please install the affiliated software into the computer and then two icons would appear on the desktop after installation The icon of SpO2 is a program for receiving real time data which is shown as figure 11 the icon of SpO2 Review is a program for receiving stored data which is shown V as figure 12 Figure 11 SpO2 program Y ypa DET EIL Figure 12 SpO2 Review program a Please connect the device to computer with the affiliated data line then double click SpO2 Review icon to start the program b On the main menu interface press the up button or down button in order to move the menu choice bar to Upload then press the menu button to transmit the stored data to computer for replay and analysis c Inthe state of storing it is not applicable forthe users to upload the stored date to computer d When the stored data is being uploaded the screen displays as figure 13 Figure 13 e When the upload of stored data is finished the device will automatically return to the main menu and the menu choice bar will move to Exit automatically as well
21. rm screen change button down button probe jack 5002 ALM HI 5002 ALM LO Figure 2 Front View 5 2 Underside View and Left View Finger 3 Underside View and Left View 1 Probe jack It is used to connect a SpO sensor to measure the oxygen saturation and pulse rate 2 USB port It is used to connect a personal computer to export the trend data or real time data or charge the lithium battery via a data line 5 3 RearView Finger 4 RearView Refer to Figure 4 and insert the lithium battery properly in the right direction 5 4 Accessories A lithium battery Model GSP053759 rated voltage 3 7 V capacity 1050mAh A User Manual A power adapter A data line A disk PC software An adult oximeter probe Model CMS 03 An infant oximeter probe May purchase selectively 7 ESOP p gt 6 Operating Guide 6 1 Application method A a Open the lid of battery box and put the battery inside then close b Putthe suitable probe into the jack on the right side of the oximeter The probe is limited to be produced by our company never replace it with the similar ones by other manufacturers c Putthe finger into the probe d Press the power on off button long about a few seconds the power is on and the device will start to self inspect The device displays the measuring interface after self inspecting e Do not shake the finger and keep the patient in a stable state during the process f The data can b
22. s moment If the alarm function is on the device will provide high priority alarm signal when the battery is in low power status Intermittent alarm will occur and the battery icon turns red in the state of flashing High priority indicating that immediate operator response is required 6 2 Attention for operation A Please check the device before using and confirm that it can work normally B The finger should be in a proper position see the attached illustration of figure 3 for reference or else it may result in inaccurate measure C The SpO sensor and photoelectric receiving tube should be arranged in a way with the subject s arteriole in a position there between D The SpO sensor should not be used at a location or limb tied with arterial canal or blood pressure cuff or receiving intravenous injection E Do not fix the SpO sensor with adhesive or else it may result in venous pulsation and inaccurate measure of SpO and pulse rate F Excessive ambient light may affect the measuring result It includes fluorescent lamp dual ruby light infrared heater direct sunlight and etc G Strenuous action of the subject or extreme electrosurgical interference may also affect the accuracy H Testee can not use enamel or other makeup I Please clean and disinfect the device after operating according to the User Manual 7 1 6 3 Clinical restrictions A As the measure is taken on the basis of arteriole pulse substantial
23. tton and confirm the setting value by pressing the menu button the black cursor will move to next place after setting When the black cursor move to Yes store or No don t store press the up button or down button to choose setting then press the menu button to confirm setting c When the Stop is displayed on menu the Do you really want to stop recording dialog box will be displayed when pressing the menu button then press the up button or down button to choose setting then press the menu button to confirm setting Ime i2 HH X TE Figure 10 d If the data storage function is being turned on when return to the measuring interface a red REC sign and a flashing red dot would appear on screen which means the device is in a state of storing e In the state of storing whatever interface the device is on measuring interface menu interface the sign Recording would appear on the screen in 30 seconds and then the screen will be automatically shut down If pressing any button power on off excluded at this moment the sign Recording would appear on the screen and then the screen will be automatically shut down again if pressing the power on off button the device would return to the former interface f Ifturning on the data storage function the former data storage will be automatically removed g In the state of data storing after the screen is automatically shut down the pulse sound indication would be off for saving p
24. xceed 195 Pulse Parameter Specification Measuring range 30bpm 250bpm the resolution is 1bpm 2bpm or 2 select larger Moving calculate the Average pulse rate every 4 cardio beat s cycle Average pulse rate The deviation between average value and true value does not exceed 1 Safety Type Interior Battery B F Type Pulse Intensity 14 Continuous bar graph display the higher display Range NP indicate the stronger pulse Battery Requirement Voltage 3 7 rechargeable lithium battery x 1 Battery working life Charge and discharge no less than 500 times Power Adapter Input Voltage 100 to 240 VAC 50 60 Hz Output voltage 5 VDC Output current 250mA Output power 1 25 W Oximeter Probe Wavelength 660nm 880nm Dimensions and Weight Dimensions 87 L x 45 W x 22 H mm Appendix 1 Guidance and manufacture s declaration electromagnetic emission for all EQUIPMENT and SYSTEMS Guidance and manufacture s declaration electromagnetic emission The Pulse Oximeter CMS60C is intended for use in the electromagnetic environment specified below The customer of the user of the Pulse Ovimeter CMS60C should assure that it is used in such an environment RF emissions The Pulse Oximeter CMS60C uses RF energy only for its CISPR 11 internal function Therefore its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment The Pulse Oximeter CMS60C is suitable
25. y is off The battery is drained away or almost Please recharge the battery suddenly drained away The device can not l 1 Please recharge the battery The battery is not full charged be used for full time 2 The battery is broken after charge center 2 Please contact the local service The battery can not be full charged even Please contact the local service The battery is broken after 10 hours center charging time 9 Key of Symbols Signal Des p Diona Ca mmm OH eem 000 OH eee 0 OB ee E NCC em 00 8 em Alarm pause button up button Mm 3 Screen change button down button Type BF 13 SN Serial number 1 the finger clip falls off no finger inserted 2 Probe error 3 Signal inadequacy indicator IPXI Ingress of liquids rank WEEE 2002 96 EC This item is compliant with Medical Device Directive 93 42 EEC of June 14 1993 a directive of the European Economic Community 10 Function Specification Information Display Mode The Pulse Oxygen Saturation SpO 2 digit digital OLED display Pulse Rate PR 3 digit digital OLED display Pulse Intensity bar graph bar graph OLED display SpO Parameter Specification Measuring range 0 100 the resolution is 1 7094 10095 2 Below 70 unspecified Calculate the Average value in every 4 measure value The deviation between average value and true value Average value does not e
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