viatom 2ADXK-6621 Checkme Lite Plus Heart Monitor ECG Monitor with Pulse Oximeter User Manual

viatom 2ADXK-6621 Checkme Lite Plus Heart Monitor ECG Monitor with Pulse Oximeter User Manual

Check me Lite Health Monitor User’s Manual

Warnings and Cautionary Advices

• We recommend not to use this device if you have a pacemaker or other implanted devices. Follow the advice given by your doctor, inapplicable.
• Do not use this device with a defibrillator.
• Do not use this device during MRI examination.
• Never submerge the device in water or other liquids. Do not cleanthedevicewithacetone or other volatile solutions.
• Do not drop this device or subject it to strong impact.
• Do not place this device in pressure vessels or gas sterilization device.
• Do not dismantle the device, as this could cause damage or malfunctionsorimpede the operation of the device.
• This device is not intended for use by people (including children) with restricted physical, sensory or mental skills or a lack of experience and/or alackofknowledge, unless they are supervised by a person who has responsibility for their safety or they receive instructions from this person on how to use the device.
• This device displays changes in the heart rhythm and blood oxygenation etc. which may have various different causes. These may be harmless, but mayalsobetriggered by illnesses or diseases of differing degree of severity. Please consult medical specialist if you believe you may have an illness ordisease.
• Do not self-diagnose or self-medicate on the basis of this devicewithoutconsulting your doctor. In particular, do not start taking any newmedicationorchange the type and/or dosage of any existing medication without prior approval.
• The device has no alarms and will not sound if the measurement readingistoolow or too high.

About Checkme

Intended Use

The Checkme Lite health monitor is intended to be used for measuring, displaying, storing and reviewing of multiple physiological parameters including ECG and pulse oxygen saturation (SpO2) in home or healthcare facilities environment. ECG is intended for use with adult.

The data and results provided by this device are for pre-check screening purpose onlyand cannot be directly used for diagnostic or treatment.

**Outline

**

1. Touch Screen

2. Internal SpO2 sensor

3. Micro-D connector
   It connects with mirco-D cable for charging.

4. Home button

   • When the monitor is off, press this button to power it on.
   • When the monitor is on, press and hold it for 2 seconds to turn it off.
   • During operation, press this button will switch to Main Screen or return to upper menu.

5. ECG right electrode (Put right thumb on it.)

6. Speaker

7. ECG left electrode (Put it to your left palm, left abdomen or left knee.)

8. Neck stripe hole

9. ECG back electrode (Put right forefinger or middle finger on it.)

Main Screen

The Main Screen is shown as below.

Press an icon in the Main Screen will start a measurement, activate a function, or open corresponding menu.

The device will enter Main Screen when:

• No operation is detected for 60 seconds in result screen, the device will automatically switch to Main Screen.
• Pressing the Home button in other screen interface.

You can change the sound volume by taping the button on theft of the screen, then tap the area. Or you can also go to the Setting menutochangeit it.

Symbols

municipal waste.
| Follow Instructions for Use.
| Type BF Applied Part
| No alarm system
| MRI unsafe. Presents hazards in all MR environments as device contains strongly ferromagnetic materials.
IP22| Resistant to liquid ingress
| CE marking
---|---
| ** Authorized representative in the European community
UK REP| ** UKCA marking
| Authorized Representative in the United Kingdom
| This product complies with the rules and regulations of the Federal Communication Commission.
| Non-ionizing radiation
| Our products and packaging can be recycled, don’t throw them away!Find where to drop them off on thewww.quefairedemesdechets.fr site (Only applicable for French market).
| This product complies with verpackG.

Getting Started

Power On/Off

Press the Home button to power on the device. Press and hold Homebuttonfor2seconds to power off thedevice.

Initial Settings

The first time when the Checkme is powered on, you can set up your Checkmestepbystep. You can also change the settings in the menu.

Using Checkme

Prior to Use Before using ECG

Before using Daily Check or ECG Recorder function, pay attention to thefollowingpointsin order to obtain precise measurements.

• If your skin or hands are dry, moisten them before taking the measurement.
• During the measurement, do not touch your body with the hand with which youare taking the measurement.
• Please note that there must be no skin contact between your right and left hand .Otherwise, the measurement cannot be taken correctly.
• Stay still during the measurement, do not speak and move.
• If possible, take the measurement when sitting instead ofstanding.

Before using Oximeter

Before using Daily Check and Oximeter function, pay attention to the followingpointsin order to obtain precise measurements.

• The finger inserted in SpO2 sensor must be clean.

• Any of the following conditions may cause inaccurate measurements, including but not limited to:

  • Flickering or very bright light;
  • Poor blood circulation;
  • Low hemoglobin;
  • Hypotension, severe vasoconstriction, severe anemia or hypothermia;
  • Nail polish, artificial nails;
  • Any tests recently performed on you that required an injection of intravascular dyes.

• The Oximeter may not work if you have poor circulation. Rub your finger to increase circulation, or place the SpO2 sensor on another finger.

• The Oximeter measures oxygen saturation of functional hemoglobin. High levels of dysfunctional hemoglobin (caused by sickle cell anemia, carbon monoxide, etc.) could affect the accuracy of the measurements.

• The pleth waveform displayed on the device is normalized.
  **** Warnings and Cautionary Advices

• Limit finger movement as much as possible when using the Daily Check or Oximeter, which might result in incorrect reading or analysis.

Daily Check About Daily Check

Warnings and Cautionary Advices

• To ensure better tracking of your health status, it is strongly suggestedthatevery Daily Check measurement is made at the same time periodwhenyourbody is in the relative same situation. E.g., every morning whenget up, oreverynight before go to bed.

Daily Check measurement is a function that combines the measuringofECG(Electrocardiograph) waveform, HR (heart rate), SpO2 (blood oxygenation) andPI (PulseIndex). It takes only 20 seconds to collect your vital signs before giving results

Using Daily Check

To start a Daily Check, follow the steps as below

1. Tap the icon in the middle of the Main screen.
2. Hold the device according to the instruction, keep the device at the same level as your heart, andkeepstableposture and stay calm. Don’t exert too much pressure on the ECG electrode ,which may result in EMG (electromyograph) interference. Just hold gently and ensure good contact with the ECG electrode. Do not exert pressureonthefingerthat put in the SpO2 sensor. Just fit it inside but gently to ensuregoodbloodperfusion.
3. Put the right forefinger into the built-in SpO2 sensor. Use the fingernail to

squeeze the edge of the SpO2 sensor cover,then move in upwardtotheleftto raise it up ashen below.

2. Press the right thumb on the right electrode.
3. Press the right middle finger on the back electrode.
4. Press the left electrode to the left palm  

3. Once the device detects stable waveform, it will automatically start the measurement. The countdown bar moves from left to right.
4. When the bar is fully filled, the device will analysis your data, and then show the measurement result.

ECG Recorder

Different methods of taking the ECG measurement are available on Check me. The ECG recorder offerstwo different methods to measuring ECG:

1. Lead I: right hand to left hand
2. Lead II: right hand to left abdomen or left knee

Please keep stable posture and stay calm during the measurement. Movementsmayresult in interference and incorrect readings or analysis result

Measuring without cable

To start an ECG Recorder measurement without cable,

1. 1. If the device is power off, press the Home button.

2. In the Main Screen, tap the icon.

3. Choose the method A or B.

4. Follow the instruction according to the mode you selected.

   • Press the right thumb on the right electrode;
   • Press the right forefinger on the back electrode;
   • For Lead I, press the left electrode to the left palm;
   • For Lead II, press the left electrode to the left lowe abdomen;

5. Once the device detects stable waveform, it will automatically start the measurement. The countdown bar moves from left to right.

6. When the bar if fully filled, the device will analysis your data, and then show the measurement result.

Measuring with Cable

To start an ECG Recorder measurement with cable,

1. If the device is power off, press the Home button.

2. In the Main Screen, tap the icon.

3. Choose the method C or D.

4. Follow the instructions to connect the ECG cable and place the ECG electrodes.

   • Sit down or stand, stay calm;
   • Palms facing up, place an electrode in the middle of right wrist;
   • For method C, place another electrode in the middle of leftwrist;
   • For method D, place another electrode in the left lower abdomen;

5. The display will then show your ECG waveform.
   The device will monitor your ECG continuously, however no data will besaveduntil you press the button.

6. Press the button to start collecting your ECG data. The countdownbarmovesfrom left to right.

7. When the bar is fully filled, the device will analysis your data, and then show the measurement result

Oximeter

The Check me Health Monitor measures the amount of oxygen in your blood(SpO2),your pulse rate (PR) and pulse index (PI). The oxygen saturation (SpO2) is measuredanddisplayed as a percentage of full capacity

Measuring without cable

To start a Oximeter measurement without cable,

1. If the device is power off, press the home button.

2. In the Main Screen, tap the “Pulse Oximeter” icon.

3. Insert the forefinger into the built-in SpO2 sensor as shown below. Relax your forefinger and do exert pressure.

4. When the device detects stable waveform, it will automatically start the measurement. The countdown bar moves from left to right.

5. When the bar is fully filled, the device will analysis your data, and then show the measurement result.

Measuring with Cable (Optional)

1. Connect the external SpO2 sensor to the multi-functional connector.

2. Put your index finger or middle finger into the external SpO2 sensor. Measure the cable is positioned along the top of the hand, and the finger nail is in the position as shown below

3. If the device is power off, press the Home button. Tap the icon.

4. The display will then show your PLETH waveform, SpO2 and pulse rate.

The device will monitor your ECG continuously, however no data will besaveduntilyou press the button.

5. Press the button to start collecting your SpO2 data. The count down bar moves from left to right.
6. When the bar is fully filled, the device will analysis your data, and then show the measurement result.

Settings

Opening Settings Menu

To open the Settings menu, tap the icon to open the menu as below.

Changing Sound Volume

In the Settings menu, tap the area to change the volume directly. Or use the quick setting by tapping the area on the left side of the screen.

Changing Brightness

In the Settings menu, tap the area to change the Brightness directly Or use the quick setting by tapping the area on the left side of the screen.

Setting Date & Time

1. Choose <Date & Time>.
2. Tap “+” or “-” button to change the date and time.

Turning on/off Voice Guide

In the Settings menu, tap the area to turn on/off voice guide directly. Or use the quick setting by tapping the area on the left side of the screen.

Choosing Language

1. In the Settings menu, choose .
2. Choose the language from the list.
3. Press the Home Button to return to the Settings menu.

Erasing Data

In the Setting menu, tap , and then . Please be noted that all measurements saved in the device will be deleted.

Factory Reset

1. In the Setting menu, choose <Factory Reset, then tap . All measurements, user information and other settings saved in the device will be deleted, and the device will be restored to the factory default settings.

Bluetooth connection

Install the latest APP on your smartphone (support BLE Bluetooth) from App Store(iOS)or Google Play (Android). Switch on the device Bluetooth in Setting- Bluetooth and run the APP, then the datawillbe downloaded automatically.

Review

To open the menu, tap the icon in Main screen.

Reviewing Daily Check

To review Daily Check records,

1. In the menu, select .
2. Select one record to review more information as below.

In this menu, you can:

• Select to delete this measurement
• Select to replay the ECG waveform as shown below.
• Select to return to the Daily Check list

Reviewing ECG Recorded

To review ECG Recorder records, in the menu, select .The operations you can perform is almost the same with Daily Check.

Reviewing Oximeter

To review Oximeter records, in the menu, select . The operations you can perform is almost the same with Daily Check.

Maintenance

Battery

This monitor is designed to operate on rechargeable Lithium-ion battery. The battery is charged automatically when the monitor is connected to a powered USB port.

On-screen battery symbols indicate the battery status as follow:
The battery is fully charged.
The solid portion represents the remained battery energy. If thesolidportion moves from left to right, then it means that the battery is being charged.
Indicates that the battery is almost depletedandneedto be charged immediately. Otherwise the device will Shut nonautomatically.

To charge the battery, connect the USB charging cable ashen.

The device cannot be used for any measurement during charging.

Use USB charging devices comply with electrical safety standard, for example IEC 60950.

Care and Cleaning

Clean the device by carefully swabbing the device surface with a soft clothswabwith water oralcohol.

Trouble Shooting

1. The battery may be low
2. The device might be damaged

|

1.  Charge the batteryand try again.
2. Please contact with yourlocal distributor.

The ECG waveform amplitude is small| The lead you choose is not suitable foryou.| Change another lead and try again.
ECG waveform drifts|

1. The pressure exerted on the electrode is not stableor too much.
2.  Hand or body may bemoving.

|

1. Hold the device stably and gently.
2. Try to keep perfectlystill and test again.

theerror persists, contactwith authorized service center.
SpO2 value is too| 1. Finger pressed toohard.| 1. Reinsert yourfinger
low when| 2. Finger may not be| gently andstably.
measured using| insertedcorrectly.| 2. Make sure your fingeris
integrated sensor.| | in right position.

Accessories

Warnings and Cautionary Advices

• Use accessories specified in this chapter. Using other accessories maycausedamage to the device or not meet the claimed specifications.

Part Number: Description
540-00192-00: ECG cable with 2leadwires
540-00194-00: USB charging cable, micro D
560-00198-00: ECG electrode, 10 pcs
540-00193-00: external SpO2 sensor(optional)

Specifications

Environmental

Item| Operating| Storage
Temperature| 5 to 45°C| -25 to 70°C
Relative humidity(noncondensing)| 10% to 95%| 10% to 95%
Barometric| 700 to 1060 hPa| 700 to 1060 hPa
Degree of dust & water resistance| IP22
Physical
Size| 88×56×13 mm
Weight| 64 g (main unit)
Display| 2.4” touch screen, color,backlit
---|---
Connector| Micro-D connector
Power Supply
Battery type| Rechargeable lithium-polymerbattery
Battery run time| Daily check: > 200 times
Charge time| Less than 2 hours to 90%
ECG
Lead type| Integrated ECG electrodes
Lead set| Lead I, lead II
Record length| 30s
Sampling| 500 Hz / 16 bit
Display Gain| 1.25 mm/mV, 2.5 mm/mV, 5 mm/mV10 mm/mV, 20 mm/mV
Sweep speed| 25 mm/s
Bandwidth| 0.67 to 40Hz
Electrode offset potentialtolerance| ±300 mV
HR measurement range| 30 to 250 bpm
Accuracy| ±2 bpm or ±2%, whichever isgreaterHeart rate is calculated based on average of every 5 to 30 QRS complex.
**** Measurement summary| Heart rate, QRS duration, Rhythm analysis (Regular ECG Rhythm, High Heart Rate, Low Heart Rate, High QRS Value,. Irregular ECG Rhythm, Unable to analyze)
Standards| Meet standards of ISO 80601-2-61
Measurement accuracy verification: The SpO2 accuracy has been verified in human experiments by comparing with arterial blood sample reference measured with a CO-oximeter. Pulse oximeter measurement are statistically distributed and about two-thirds of the measurements are expected to come within the specified accuracyrange compared to CO-oximeter measurements.
SpO2 range| 70% to 100%
SpO2 Accuracy(Arms)| 80-100%:±2%, 70-79%:±3%
PR range| 30 to 250 bpm
PR accuracy| ±2 bpm or ±2%，whichever isgreater
PI range| 0.5-15
Measurement summary| SpO2, PR, PI, Summary (Normal Blood Oxygen, Low Blood Oxygen, Unable to analyze)

Electromagnetic Compatibility

The device meets the requirements of EN 60601-1-2. All the accessories also meet there querulents of EN 60601-1-2 when in use with this device.

Warnings and Cautionary Advices

• Using accessories other than those specified in this manual may result in increased electromagnetic emission or decreased electromagnetic immunity of the equipment.
• The device or its components should not be used adjacent to or stacked with other equipment.
• The device needs special precautions regarding EMC and needs to be installed and put into service according to the EMC information provided below.
• Other devices may interfere with this device even though they meet the requirements of CISPR.
• When the inputted signal is below the minimum amplitude provided in technical specifications, erroneous measurements could result.
• Portable and mobile communication equipment may affect the performance of this device.
• Other devices that have RF transmitter or source may affect this device (e.g. cell phones, PDAs, and PCs with wireless function).

Guidance and Declaration – Electromagnetic Emissions

The Health Monitor is intended for use in the electromagnetic environment specified below. The customer or theuser of the device should assure that it is used in such an environment.
Emission tests| Compliance| Electromagnetic environment – guidance
RF emissions CISPR 11| Group 1| The device uses RF energy only for its internal function. Therefore, its RF emissions are very low and are not likelyto cause any interference in nearby electronic equipment.
RF emissions CISPR 11| Class B| The device 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.
Harmonic emissions IEC61000-3-2| Class A
Voltage Fluctuations / FlickerEmissions IEC 61000-3-3| Complies
Guidance and Declaration – Electromagnetic Immunity
The Health Monitor is intended for use in the electromagnetic environment specified below. The customer or theuser of the Health Monitor should assure that it is used in such an environment.
Immunity test| IEC60601 test level| Compliance level| Electromagnetic environment – guidance
Electrostatic discharge (ESD) IEC 61000-4-2| ± 6 kV contact± 8 kV air| ± 6 kV contact± 8 kV air| Floors should be wood, concrete or ceramic tile. If floors are covered withsynthetic material, the
| | | relative humidity should be atleast 30 %.
---|---|---|---
Electrical fast transient/burst IEC 61000-4-4| ± 2 kV for power supply lines± 1 kV for input/output lines| ± 2 kV for power supply lines± 1 kV for input/output lines| Mains power quality should be that of a typical commercial or hospital environment.
SurgeIEC 61000-4-5| ± 1 kV line(s) to line(s)± 2 kV line(s) to earth| ± 1 kV line(s) to line(s)± 2 kV line(s) to earth
Voltage dips, short Interruptions and Voltage variations on power supply input linesIEC 61000-4-11| <5 % UT(>95 % dip in UT) for 0.5 cycle40 % UT(60 % dip in UT) for 5 cycles70 % UT(30 % dip in UT) for 25 cycles<5 % UT(>95 % dip in UT) for 5 s| <5 % UT(>95 % dip in UT) for 0.5 cycle40 % UT(60 % dip in UT) for 5 cycles70 % UT(30 % dip in UT) for 25 cycles<5 % UT(>95 % dip in UT) for 5 s| Mains power quality should be that of a typical commercial or hospital environment. If the user of our product requires continued operation during power mains interruptions, it is recommended that our product be powered from an uninterruptible power supply or a battery.
Power frequency (50/60 HZ) magnetic field IEC 61000-4-8| 3 A/m| 3 A/m| Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospitalenvironment.
Note: UT is the AC mains voltage prior to application of the test level.
Guidance and Declaration – Electromagnetic Immunity
The Health Monitor is intended for use in the specified electromagnetic environment. The customer or the user ofthe Health Monitor should assure that it is used in such an environment as described below.
Immunity test| IEC60601 test level| Compliance level| Electromagnetic environment – guidance
Conduced RF IEC61000-4-6| 3 Vrms 150 kHz to80 MHzoutside ISM bands| 3 Vrms 150 kHz to80 MHzoutside ISM bands| Portable and mobile RF communications equipment should be used no closer to any part of the system, including cables, than the recommended separation distance calculated from the equation appropriate for the frequency of the transmitter. Recommended separationdistances: d = 1 . 2 P
Radiated RF IEC61000-4-3| 3 V/m 80MHz to 2.5 GHz| 3 V/m 80MHz to 2.5 GHz| Recommended separation distances:80 MHz～800 MHz:    d = 1 . 2      P 800MHz-2.5GHz:    d = 2 . 3     P Where, P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and d is the recommended separation distance in meters (m).Field strengths from fixed RF transmitters, as determined by an electromagnetic site survey a, should be less than the compliance level in each frequency range b.Interference may occur in the vicinity of equipmentmarked with the following symbol:
Note 1: At 80 MHz to 800 MHz, the separation distance for the higher frequency range applies.
Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption andreflection from structures, objects and people.

a Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV 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 device is used exceeds the applicable RF compliance level above, the device should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as re-orienting or relocating the device.b Over frequency range 150kHz to 80MHz. For Resp field strength should be less than 1V/m.
Recommended separation distances between portable and mobile RF communications equipment and thedevice
The Health Monitor is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the Health Monitor can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) andthe monitor as recommended below, according to the maximum output power of the communications equipment.
Rated max. output power of transmitter (W)| Separation distance according to frequency of the transmitter (m)
150 kHz – 80 MHz d = 1.2 P| 80 MHz – 800MHz d = 1.2 P| 800 MHz – 2.5 GHz d = 2 .3 P
0.01| 0.12| 0.12| 0.23
0.1| 0.38| 0.38| 0.73
1| 1.20| 1.20| 2.30
10| 3.80| 3.80| 7.30
100| 12.00| 12.00| 23.00
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in metres (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 1: At 80 MHz and 800 MHz, the separation distance for 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.

FCC Statement

FCC Warning:

FCC ID : 2ADXK-6621

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

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.

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.

The device has been evaluated to meet general RF exposure requirement. The device can be used in portable exposure condition without restriction,

Shenzhen Viatom Technology Co., Ltd. 4E, Building 3, Tingwei Industrial Park, No.6 Liufang Road, Block 67, Xin’an Street, Baoan District, Shenzhen, 518101, Guangdong, China

Med Net EC-REP GmbH
Bork Strasse 10, 48163 Muenster, Germany
Tel: +49 251 32266-0
Fax:  +49 251 32266-22
Email: contact@mednet-ecrep.com

MediMap Ltd
2 The Drift, Thurston, Suffolk IP31 3RT, United KingdomTel: +49 251 32266-0
Fax: +49 251 32266-22
Email: contact@mednet-ecrep.com

PN：255-00233-00 Version: G Apr, 2022
Contents of this manual are subject to changes without priornotice.
©Copyright 2014-2017 Shenzhen Viatom Techno logy Co., Ltd. All rights reserved.

Read User Manual Online (PDF format)

Read User Manual Online (PDF format)  >>

Download This Manual (PDF format)

Download this manual  >>