ShenZhen Jumper Medical Equipment JPD500G Pulse Oximeter User Manual JPD 100A

ShenZhen Jumper Medical Equipment Co.,Ltd Pulse Oximeter JPD 100A

User Manual

Pulse Oximeter JPD-500G(Bluetooth)FCC statementThis device complies with Part 15 of the FCC Rules. Operation is subjectto the following two conditions :(1) This device may not cause harmful interference.(2) This device must accept any interference received,including interference thatmay cause undesired operation.NOTE: This equipment has been tested and found to comply with the limitsfor a Class B digital device, pursuant to Part 15 of the FCC Rules. These limitsare designed to provide reasonable protection against harmful interference ina residential installation. This equipment generates, uses and can radiateradio frequency energy and, if not installed and used in accordancewith the instructions, may cause harmful interference to radio communications.However, there is no guarantee that interference will not occur in a particularinstallation. If this equipment does cause harmful interference to radio ortelevision reception, which can be determined by turning the equipment offand on, the ser is encouraged to try to correct the interference by one or moreof 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 towhich the receiver is connected.●Consult the dealer or an experienced radio/TV technician for help.Warning: Changes or modifications to this unit not expressly approved by theparty responsible for compliance could void the user’s authority to operatethe equipment.PrecautionsDo not attempt to repair he Oximeter unless you are professional engineers. Onlyprofessionals with maintenance qualification are allowed to perform interiormaintenance as necessary.Change the contact position between the Oximeter probe and the fingerperiodically if you are monitoring your SpO2 levels and pulse rate for more than 2hours.Stop immediately if you have broken skin or the blood circulation of your finger isaffected during prolong use.This product is not designed to be used by newborn babies.Seek for medical care if the measured value goes beyond the normal range and youare sure that the instrument is not malfunctioning.The pulse oximeter uses infrared light (invisible to your eyes) to measure yourSpO2 levels. Hence, please do not stare at the light-emitting components of theOximeter, as that could cause harm and/or potentially blind your eyes.This pulse oximeter is not a medical device and is not intended to diagnose ortreat any medical condition or disease. It is intended for non-medical use in healthypeople to monitor their pulse and blood oxygen levels during sports and/or aviationonly.People who need SpO2 and pulse rate measurements because of a medicalcondition should not use the oximeter and should consult with their physician.For details about clinical limitations and contraindications,please carefully consultrelevant medical literatures.The following factors may affect the accuracy of the measurement:The Oximeter is used in an environment involving high-frequency devices,such as high-frequency electric knives and CT apparatuses.Ambient light intensity is too bright. Hence, please avoid direct exposure tostrong light (such as beams from operating lamps or sunlight) duringmeasurement.The probe of the Oximeter is placed on the same arm that a blood pressurecuff arterial duct or intravenous injection.The user suffers from hypotension, severe vascular atrophy, severe anemia,or low oxygen.The user is in sudden cardiac arrest or shock state.The user is wearing nail polish or artificial nails.WarningsWarning: Do not use the Oximeter in an environment with any flammable gases,flammable anesthetic, or other flammable substances.Warning: Keep unit and lanyard away from children as the included lanyard maypresent an entanglement or choking hazard to small children. Adult supervisionrequired; never leave children unattended with unit or lanyardWarning: Do not throw the batteries into fire, as that could cause an explosion.Warning: Do not attempt to charge the included batteries, as that could causeleakage, fire disaster, or even explosion. Dispose the used batteries in accordance tothe local laws and regulations.Warning: Do not use the Oximeter in an MRI or CT environment.Warning: Caution: Do not operate the Oximeter if it is wet. Avoid moving theoximeter from a cold to a hot and humid environment.Warning: Install the batteries properly before powering on the Oximeter for normaluse. Please remove the batteries if you are not planning to use the Oximeter for along time.Warning: Close the battery cover when the instrument is in use.SymbolsSymbolMeaningType BF applied partCaution: Please see this manual.%SpO2Symbol of oxygen saturationbpmPRSymbol of pulse rateNo SpO2 alarms.BluetoothWhen end users abandon this product, they must sendthe product to the collection place for recycling.OverviewOxygen saturation is the percentage of oxyhemoglobin (HbO2) that is combinedwith oxygen against all combinable hemoglobin (Hb). It is an important physiologicalparameter involved in respiration and circulation. The oxygen saturation of arterialblood in a normal human body is 98%. Oxygen saturation is an important indicatorof the oxygen condition in the human body. In general, the normal values of oxygensaturation shall not be lower than 94%. If the measured value of oxygen saturationis lower than 94%, an insufficient supply of oxygen is considered.The pulse rate is the number of pulse beats per minute. Normally, the pulse rate isconsistent with the heart rate. In general, the pulse rate of every people is 60 to 90beats per minute.The Perfusion Index (PI) usually reflects the limb perfusion status of an examinedpatient, and shows the detection precision of the instrument as well; that is,examination can still be performed even in the low or weak perfusion condition.ThePI of a normal human body is 3% or greater.Working Principles and UsageBased on full digital technology, the Finger Pulse Oximeter non-invasively measuresthe actual content (oxygen saturation) of oxyhemoglobin (HbO2) in arterial bloodusing the optical transmittance method.The Finger Pulse Oximeter measures the blood oxygen saturation and pulse rate ofa human body via finger artery. It is applicable to a wide range of fields, such asfamilies,clinics , oxygen bars, social medical care institutions, and sports & health.Use this instrument for measurement before or after sports. You are not advised touse this instrument during sports activities. Do not use it for continuous care forpatients.Schematic Diagram of DisplaySchematic Diagram of DisplayThe following figure shows the information display on the LED screen of theOximeter in normal detection state:Power-On button/Function Button OperationsPress the power-on/function button to turn on the oximeter.Once the it is turnedon.Simply press or hold the button to perform corresponding operations.Press: Press the button for less than 0.5 seconds.Hold: Press the button for more than 0.5 seconds.
Brightness SettingHold the power-on button while the oximeter is in powered-on state,then theoximeter shows a brightness setting interface(as "Interface 1" below shows, "br"represents brightness).Hold the button to adjust brightness. There 3 brightnesssettings(1,2,3). 3 is the brightest.Interface1Alarm SettingAfter setting the brightness,press the power-on button to enter the alarm settinginterface(as "interface 2" below shows, "AL" represents alarm).Then hold thebutton to set "AL" to on or off.When "AL" is set to on and the measured values ofthe blood oxygen saturation and pulse rate go beyond the upper limit or lowerlimit,the oximeter will beep to alarm.Interface 2Alert Range SettingWhen "AL" is set to on, you can set the upper limit and lower limit of SpO2 Alertand PR Alert. Press it to switch an option(SpO2 upper limit, SpO2 lower limit, PRupper limit and PR lower limit).Hold the power-on button to adjust the limits.(as"Interface 3,4,5,6" below show, "Hi" represents upper limit, "Lo" represents lowerlimit) .Interface 3 Interface 4Interface 5 Interface 6Operation GuideStick one finger completely into the finger chamberof the oximeter. The fingernail should be facing upward.Release the clip and press the power-on button to poweron the pulse oximeter.If you do not insert your finger completely into thechamber, measurement will be inaccurate.To keep your finger still during measurement. It is also not advisable to use thisinstrument during sports activities as movement may lead to inaccuracies. Once thereading stabilizes, read the measured values of oxygen saturation and pulse rate onthe screen.NOTE:The oximeter will automatically shut down 10 seconds after you remove yourfinger.Connecting the Instrument to a smartphone via BluetoothNote: For details on specific operations, see the JUMPER Health User Manual.Replace the batteries when the batteries run out of power and the symbolflickers on the screen.Install the two AAA dry batteries into the battery slot according to polarityindication, and mount the battery cover.CleaningPower off the instrument and remove the batteries before cleaning. Ensure that theappearance of the instrument is neat, dust-free, and dirt-free. Clean the outersurface of the instrument (including the LED screen) using a piece of dry soft clothdipped with 75% medical alcoholCaution: Avoid liquid flowing into the instrument during cleaning.Caution: Do not immerse any part of the instrument into any liquid.DisinfectionBefore measurement with the instrument, wipe the rubber finger pad using a pieceof dry soft cloth dipped with 75% medical alcohol. Clean the finger to be measuredusing the medical alcohol for disinfection purposes before and after use.Do not disinfect the instrument by means of high-temperature/high-pressure or gas disinfection.MaintenanceRemove the batteries from the battery slot and properly store them if you donot plan to use the Oximeter for a long period of time.Avoid using the Oximeter in an environment with inflammable gases or using itin an environment where the temperature or humidity is excessively high orlow.Check the accuracy of the oxygen saturation and pulse rate readings by usingan appropriate calibration apparatus.Technical Specifications1. Dimensions: 58.0 mm (Width) × 32.0 mm (Depth) × 32.9 mm (Height)Weight: 50.4 g (including two AAA dry batteries)2. Peak wavelength range of the light emitted from the probe: red light 663 nm ±3; infrared light 900 nm ± 7.3. Maximum optical output power of the probe: 60 mW for infrared light (905nm).4. Bluetooth module:4.25. Normal working conditionWorking Temperature5C to 40C(41F to 104F)Relative Humidity15% to 80%, non-condensingAtmospheric Pressure70 kPa to 106 kPaRated VoltageDC 3.0 V6. Default values and conditions of alertParameterValueOxygen saturationUpper limit: 99Lower limit: 94Pulse rateUpper limit: 130Lower limit: 50Alert conditionWhen the alert switch is on and theactual measured value goes beyondthe preset alert parameter range, theOximeter gives an alert sound.7. Technical parametersParameterValueDisplay rangeOxygensaturation35% to 99%Pulse rate35 bpm to 250 bpmResolutionOxygensaturation1%Pulse rate1 bpmMeasurementprecisionOxygensaturation±2% (70% to 99%)No requirement (≤ 69%)Pulse rate±2 bpmAlert rangeOxygensaturationUpper limit: 50% to 100%Lower limit: 50% to 100%Pulse rateUpper limit: 35 bpm to 250 bpmLower limit: 35 bpm to 250 bpmAlert errorOxygensaturation± 1% of the preset valuePulse rateThe greater of ±10% of thepreset value and ±5 bpmPIWeak PIMin. 0.3%Safety TypeAnti-electric-shock type: internal power supply deviceAnti-electric-shock degree: Type BF applied partRunning mode: continuous workingWaterproof grade: IP22Storage and TransportationTemperature : –10C - 50C(14℉-122℉)Relative humidity : 10%-93% (no condensation)Atmospheric pressure : 50kPa–106 kPa.ELECTROMAGNETIC COMPATIBILITY (EMC) TABLESGuidance and manufacturer’s declaration - electromagnetic emissionsThe device is intended for use in the electromagnetic environment specified below.The customer or the user assure that it is used in such an environment.Emissions testComplianceElectromagnetic environment - guidanceRF emissionsCISPR11Group 1The devuce device use RF energy onlyfor its internal function. Therefore, its RFemissions are very low and are not likelyto cause any interference in nearbyelectronic equipment.RF emissionsCISPR11Class BThe device is suitable for use in allestablishments other than domestic and
those directly connected to the publiclow-voltage power supply network thatsupplies buildings used for domesticpurposesHarmonicemissionslEC61000-3-2Not applicableVoltagefluctuations/FickeremissionslEC61000-3-3Not applicableGuidance and manufacturer’s declaration — electromagnetic immunityThe device is intended for use in the electromagnetic environment specified below.The customer or the user of the device should assure that it is used in such anenvironment.Immunity testIEC 60601Test levelCompliancelevelElectromagneticenvironment-guidanceElectrostaticdischarge (ESD)lEC61000-4-2±6kVcontact±8kV air±6kV contact±8kV airFloors should be wood ,concrete or ceramic tile. Iffloors are covered withsynthetic material, therelative humidity should beat least 30%Electrical fasttransient/burstIEC 61000-4-4±2 kV forpowersupply lines± 1 kVInput/output linenot applicablenot applicable(For INTERNALLY POWEREDME EQUIPMENT)SurgeIEC 61000-4-5± 1 kVDifferentialmodevoltage± 2 kVCommonmodevoltagenot applicablenot applicable(For INTERNALLY POWEREDME EQUIPMENT)Voltage dips,shortinterruptionsand voltagevariations onpower supplyinput linesIEC 61000-4-11<5% UT(>95% dipin UT)for 0.5cycle40% UT(60% dip inUT)for 5 cycles70% UT(30% dip inUT)for 25cycles<5% UT(>95% dipnot applicablenot applicable(For INTERNALLY POWEREDME EQUIPMENTin UT)for 5 secPower frequency(50Hz/60Hz)magnetic fieldIEC 61000-4-83A/m3A/mPower frequency magneticfields should be at levelscharacteristic of a typicallocation in a typicalcommercial or hospitalenvironment.NOTE UT is the a.c. mains voltage prior to application of the test level.Guidance and manufacture’s declaration – electromagnetic immunityThe device is intended for use in the electromagnetic environment specified below.The customer or the user of device should assure that it is used in such anenvironment.ImmunitytestIEC60601testlevelCompliancelevelElectromagnetic environment -guidanceRadiated RFIEC61000-4-33 V/m80 MHzto 2.5GHz3 V/mPortable and mobile RFcommunications equipment shouldbe used no closer to any part of theBlood Pressure Monitor, includingcables, than the recommendedseparation distance calculated fromthe equation applicable to thefrequency of the transmitter.Recommended separation distancePd 2.1Pd 2.180 MHz to 800 MHzPd 2.1800 MHz to 2.5 GHzWhere P is the maximum outputpower rating of the transmitter inwatts (W) according to thetransmitter manufacturer and d is therecommended separation distance inmetres (m).Field strengths from fixed RFtransmitters, as determined by anelectromagnetic site survey,a shouldbe less than the compliance level ineach frequency range.bInterference may occur in the vicinityof equipment marked with thefollowing symbol:NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies.NOTE 2 These guidelines may not apply in all situations. Electromagneticpropagation is affected by absorption and reflection from structures, objects andpeople.a Field strengths from fixed transmitters, such as base stations for radio(cellular/cordless) telephones and land mobile radios, amateur radio, AM and FMradio broadcast and TV broadcast cannot be predicted theoretically with accuracy.To assess the electromagnetic environment due to fixed RF transmitters, anelectromagnetic site survey should be considered. If the measured field strength inthe location in which the Blood Pressure Monitor is used exceeds the applicable RFcompliance level above, the Blood Pressure Monitor should be observed to verifynormal operation. If abnormal performance is observed, additional measures maybe necessary, such as reorienting or relocating the Blood Pressure Monitor.b Over the frequency range 150 kHz to 80 MHz, field strengths should be lessthan [Vi] V/m.Recommended separation distances between portable and mobile RFcommunications equipment and the device.The device is intended for use in an electromagnetic environment in which radiatedRF disturbances are controlled. The customer or the user of the device can helpprevent electromagnetic interference by maintaining a minimum distance betweenportable and mobile RF communications equipment (transmitters) and the deviceas recommended below, according to the maximum output power of thecommunications equipment.Maximum outputpower oftransmitter(W)Separation distance according to frequency of transmitter(m)80 MHz to 800MHzPd 2.1800 MHz to 2.5GHzPd 2.1800 MHz to 2.5GHzPd 2.10.01/0.120.230.1/0.380.731/1.22.310/3.87.3100/1223For transmitters rated at a maximum output power not listed above, Therecommended separation distance d in meters(m) can be estimated using theequation applicable to the frequency of the transmitter, where P is the maximumoutput power rating of the transmitter in watts(W) accordable to the transmittermanufacturer.NOTEI At 80 MHz and 800 MHz. the separation distance for the higher frequencyrange applies.NOTE2 These guidelines may not apply in all situations. Electromagneticpropagation is affected by absorption and refection from structures, objects andpeople.Wellkang LtdSuite B, 29Harley Street, LONDON, W1G9QR,U.K.Shenzhen Jumper Medical Equipment Co., LtdAddress: D Building, No. 71, Xintian Road, Fuyong Street,Baoan,Shenzhen, Guangdong,ChinaE-mail: info@jumper-medical.comTel: +86-755-26692192,26696279Web:www.jumper-medical.com

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