Pylo PY-802-LTE LTE Blood Pressure Monitor User Manual

**Pylo PY-802-LTE LTE Blood Pressure Monitor User Manual

**

Thank you for choosing Pylo Health!
This manual outlines how to use your Pylo blood pressure monitor safely and correctly. Please be sure to read it thoroughly and keep it for future reference.

INTRODUCTION

General Description

Thank you for selecting the Pylo PY-802-LTE arm type blood pressure monitor.
The monitor features blood pressure measurement, pulse rate measurement and digital result storage. Readings taken by the PY-802-LTE are equivalent to those obtained by a trained observer using the cu and stethoscope auscultation method. This manual contains important safety and care information, and provides step by step instructions for using the product.

Please read this manual thoroughly before using the product.
Features:

• 78*92mm Digital LCD display
• Measuring during inflation technology
• LTE-M wireless communication

Indications for Use

The Pylo PY-802-LTE is a digital blood pressure monitor intended for use in measuring blood pressure and heartbeat rate on users with an arm circumference ranging from 22cm to 42cm (about 8¾˝-16½˝).
It is intended for adult indoor use only.

Contraindications

1. The device should not be used by any person who is suspected to be or is pregnant unless directed to by their physician.
2. This device contains magnets as well as components and radios that emit electromagnetic fields which may interfere with medical devices, such as pacemakers and defribalators.

Consult your physician and medical device manufacturer for information specific to your medical device and whether you need to maintain a safe distance from electromagnetic fields produced by this device and other devices that utilize a cellular network connection.

Measurement Principle

This product uses the Oscillometric Measuring Method to detect blood pressure.
Before every measurement, the unit establishes a “zero point” equivalent to the atmospheric pressure prior to inflating the cu. Meanwhile, the unit detects pressure oscillation generated by beat-to-beat pulsatile, which is used to determine the systolic pressure and diastolic pressure as well as pulse rate.

Safety Information

The signs below might be in the user manual, labeling or other components.
They are the requirement of standard and using.

| Symbol for “THE OPERATION GUIDE MUST BE READ”| | Symbol for “TYPE BF APPLIED PARTS”
---|---|---|---
| Symbol for “MANUFACTURER”|         | Symbol for “ENVIRONMENT PROTECTION – Electrical waste products should not be disposed of with household waste. Please recycle where facilities exist. Check with your local authority or retailer for recycling advice”
| Symbol for “SERIAL NUMBER”
| Symbol for “DIRECT CURRENT”
| Symbol for “RECYCLE”| | Symbol for “MANUFACTURE DATE”
****| Caution: These notes must be observed to prevent any damage to the device.| |

CAUTION

• This device is intended for adult use in homes only.

• The device is not suitable for use on neonatal patients, pregnant women,patients with implanted, electronical devices, patients with pre-eclampsia, premature ventricular beats, atrial fibrillation, peripheral, arterial disease and patients undergoing intravascular therapy or arterio-venous shunt or people who received a mastectomy. Please consult your doctor prior to using the unit if you suer from illnesses.

• The device is not suitable for measuring the blood pressure of children. Ask your doctor before using it on older children.

• The device is not intended for patient transport outside a healthcare facility.

• The device is not intended for public use.

• This device is intended for no-invasive measuring and monitoring of arterial blood pressure.
  It is not intended for use on extremities other than the arm or for functions other than obtaining a blood pressure measurement.

• Do not confuse self-monitoring with self-diagnosis. This unit allows you to monitor your blood pressure.Do not begin or end medical treatment without asking a physician for treatment advice.

• If you are taking medication,consult your physician to determine the most appropriate time to measure your blood pressure. Never change a prescribed medication without consulting your physician.

• Do not take any therapeutic measures on the basis of a self measurement. Never alter the dose of a medicine prescribed by a doctor. Consult your doctor if you have any question about your blood pressure.

• When the device is used to measure patients who have common arrhythmias such as atrial or ventricular premature beats or atrial fibrillation, the best result may occur with deviation.
  Please consult your physician about the result.

• Don’t kink the connection tube during use, otherwise, the cu pressure may continuously increase which can prevent blood flow and result in harmful injury to the PATIENT.

• When using this device, please pay attention to the following situation which may interrupt blood flow and influence blood circulation of the patient, thus cause harmful injury to the patient: connection tubing kinking too frequent and consecutive multiple measurements; the application of the cu and its pressurization on any arm where intravascular access or therapy, or an arterio-venous (A-V) shunt, is present; inflating the cu on the side of a mastectomy.

• Warning: Do not apply the cu over a wound; otherwise it can cause further injury.

• Do not inflate the cu on the same limb which other monitoring ME equipment is applied around simultaneously, because this could cause temporary loss of function of those simultaneously-used monitoring ME equipment.

• On the rare occasion of a fault causing the cu to remain fully inflated during measurement, open the cu immediately. Prolonged high pressure (cu pressure > 300mmHg or constant pressure ? 15mmHg for more than 3 minutes) applied to the arm may lead to an ecchymosis.

• Please check that operation of the device does not result in prolonged impairment of patient blood circulation.

• When measurement, please avoid compression or restriction of the connection tubing.

• The device cannot be used with HF surgical equipment at the same time.

CAUTION

• The ACCOMPANYING DOCUMENT shall disclose that the SPHYGMOMANOMETER was clinically investigated according to the requirements of ISO 81060-2:2013.

• To verify the calibration of the AUTOMATED SPHYGMOMANOMETER, please contact the manufacturer.

• This device is contraindicated for any female who may be suspected of, or is pregnant. Besides providing inaccurate readings, the eects of this device on the fetus are unknown.

• Too frequent and consecutive measurements could cause disturbances in blood circulation and injuries.

• This unit is not suitable for continuous monitoring during medical emergencies or operations. Otherwise, the patient’s arm and fingers will become anaesthetic, swollen and even purple due to a lack of blood.

• When not in use, store the device in a dry room and protect it against extreme moisture, heat, lint, dust and direct sunlight. Never place any heavy objects on the storage case.

• This device may be used only for the purpose described in this booklet. The manufacturer cannot be held liable for damage caused by incorrect application.

• This device comprises sensitive components and must be treated with caution. Observe the storage and operating conditions described in this booklet.

• The equipment is not AP/APG equipment and not suitable for use in the presence of a flammable anesthetic mixture with air of with oxygen or nitrous oxide.

• Warning: No servicing/maintenance while the ME equipment is in use.

• The patient is an intended operator.

• The patient can measure, and charge power under normal circumstances and maintain the device and its accessories according to the user manual.

• To avoid measurement errors, please avoid the condition of strong electromagnetic field radiated interference signal or electrical fast transient/burst signal.

• The blood pressure monitor, and the cu are suitable for use within the patient environment.
  If you are allergic to polyester, nylon or plastic, please don’t use this device.

• During use, the patient will be in contact with the cu. The materials of the cu have been tested and found to comply with requirements of ISO 10993-5:2009 and ISO 10993-10:2010.
  It will not cause any potential sensation or irritation reaction.

• \Adaptor is specified as a part of ME EQUIPMENT.

• If you experience discomfort during a measurement, such as pain in the arm or other complaints, press any button to release the air immediately from the cu. Loosen the cu and remove it from your arm.

• If the cu pressure reaches 40 kPa (300 mmHg), the unit will automatically deflate. Should the cu not deflate when pressure reaches 40 kPa (300 mmHg), detach the cu from the arm and press any button to stop inflation.

• Before use, make sure the device functions safely and is in proper working condition. Check the device, do not use the device if it is damaged in any way. The continuous use of a damaged unit may cause injury, improper results, or serious danger.

• Do not wash the cu in a washing machine or dishwasher!

CAUTION

• The service life of the cu may vary by the frequency of washing, skin condition, and storage state. The typical service life is 10000 times.

• It is recommended that the performance should be checked every 2 years and a²er maintenance and repair, by retesting at least the requirements in limits of the error of the cu pressure indication and air leakage (testing at least at 50mmHg and 200mmHg).

• Please dispose of ACCESSORIES, detachable parts, and the ME EQUIPMENT according to the local guidelines.

• Manufacturer will make available on request circuit diagrams, component part lists, descriptions, calibration instructions,etc., to assist to service personnel in parts repair.

• The plug/adapter plug pins insulate the device from the main supply. Do not position the device in a position where it is diicult to disconnect from the supply mains to safely terminate operation of ME equipment.

• The operator shall not touch output of batteries /adapter and the patient simultaneously.

• Cleaning : Dust environment may aect the performance of the unit. Please use the so² cloth to clean the whole unit before and a²er use. Don’t use any abrasive or volatile cleaners.

• The device doesn’t need to be calibrated within two years of reliable service.

• If you have any problems with this device, such as setting up, maintaining or using, please contact the SERVICE PERSONNEL of Pylo. Don’t open or repair the device by yourself in the event of malfunctions. The device must only be serviced, repaired and opened by individuals at authorized sales/service centers.

• Please report to Pylo if any unexpected operation or events occur.

• Keep the unit out of reach of infants, young children or pets to avoid inhalation or swallowing of small parts. It is dangerous or even fatal.

• Be careful to strangulation due to cables and hoses, particularly due to excessive length.

• At least 30 min required for ME equipment to warm from the minimum storage temperature between uses until it is ready for intended use. At least 30 min required for ME equipment to cool from the maximum storage temperature between uses until it is ready for intended use.

• This equipment needs to be installed and put into service in accordance with the information provided in the ACCOMPANYING DOCUMENTS;

• Wireless communications equipment such as wireless home network devices, mobile phones, cordless telephones and their base stations, walkie-talkies can aect this equipment and should be kept at least a distance d away from the equipment. The distance d is calculated by the MANUFACTURER from the 80MHz to 5.8 GHz column of Table 4 and Table 9 of IEC 60601-1-2:2014, as appropriate.

• Please use ACCESSORIES and detachable parts specified/ authorised by MANUFACTURER.
  Otherwise, it may cause damage to the unit or danger to the user/patients.

• There is no luer lock connectors are used in the construction of tubing, there is a possibility that they might be inadvertently connected to intravascular fluid systems, allowing air to be pumped into a blood vessel.

• Please use the device under the environment which is provided in the user manual.
  Otherwise, the performance and lifetime of the device will be impacted and reduced.

LCD Display Signal

SYMBOL

| DESCRIPTION|

EXPLANATION

---|---|---
SYS| Systolic blood pressure| High pressure result
**DIA**  | Diastolic blood pressure| Low pressure result
Pulse/min| Pulse| Pulse/minute
| Current Time| Time (year: month: day: hour: minute)
| Heartbeat| Heartbeat detection during measurement
mmHg| mmHg| Measurement Unit of the blood pressure
| Battery Indicator| Indicate the current battery
| Irregular heartbeat| Irregular heartbeat
| Data transmission indication| Indicates that the data is being sent. oH will show on screen to indicate success.
| Shocking reminder| Sudden movement will result in inaccurate readings
****| Signal indication| Indicates the signal situation in the communication process.

Components of the Device

Component list of pressure measuring system:

1. Cu
2. Air pipe
3. PCBA
4. Pump

Included Parts List

1. Cellular Blood Pressure Monitor (PY-802-LTE)

2. Cu (22~42cm) (Type BF applied part)

3. User manual

4. Four (4) AA batteries

BEFORE YOU START

The Choice of Power Supply

1. Battery powered mode: 6VDC 4*AA batteries
2. C adaptor powered mode: 6V ****1A (not included)
   (Please only use a manufacturer authorized AC adapter.) See picture on right hand side for power port location.

CAUTION
In order to get the best eect and protect your monitor, please use the the right batteries and special power adapter which complies with local safety standard.

Installing and Replacing the Batteries
If this is your first time using the device:

1. Slide open the battery door on the back of the device.
2. Install the batteries provided with the device. Follow the diagram inside the battery compartment for correct placeme—the springs should align with the negative sign on the batteries.
3. Slide the battery door closed.

Replace the batteries whenever the following occurs:

• The icon displays
• The display dims
• The display does not light up

CAUTION

• Do not use new and used batteries together.

• Do not use dierent types of batteries together.

• Do not dispose the batteries in fire. Batteries may explode or leak.

• Remove batteries if the device is not likely to be used for some time.

• Used batteries are harmful to the environment.
  Do not dispose with daily garbage.

• Remove the old batteries from the device following your local recycling guidelines.

Tip:
When you insert or replace batteries into the device, the symbol and  will be shown on the LCD. This indicates that the device is searching and pairing with a mobile network. You can long press “ START/STOP ” button to end pairing and use the device. If you manually cancel pairing, the device may take longer to send a measurement a²er use..
When pairing is successful, the symbol is shown on the display. You can then utilize the device as normal by pressing “START”.

MEASUREMENT

Tie the Cuff

1. Plug the connector into the ‘Cu Port’ as labeled on the device.
   

2. Expose your upper arm by removing or adjusting clothing and jewelry. Make sure blood flow is not constricted by a rolled up sleeve.

3. Open the cu and loosen fully.

4. Orient the cu so that the tube exits towards the hand.

5. Place your arm through the cu loop, with your palm facing up.
   

6. Position the cu’s edge about an inch (2–3 cm) above the elbow.

7. Align the Ф marker (located to the right of the tube exit) with the center of your arm.

8. Tighten the cu evenly around your arm by pulling on the end—make sure the Ф marker stays aligned with the center of your arm.

9. Wrap the end of the cu over your arm to secure it in place. Don’t make it too tight—allow a finger to fit between the cu and your arm.

10. If possible, relax and rest for at least 5 minutes before taking a measurement.
    

11. Lay your arm on a table with your palm facing up.
    The cu should be at the same height as your heart.
    Sit up straight and rest your feet flat on the ground. Make sure the tube is not kinked or pinched.

Taking a Measurement

1. When the monitor is o, press the “ START/STOP ” button to turn on the monitor. The cu will begin to inflate and the measurement will be taken and saved.

LCD display

Adjust the zero

Inflating and measuring

Display and save the results

2. Once measurement is taken, the device will connect to the network and start transmission.
   The symbol will blink while the device is transmitting.

3. If the data is successfully transmitted, the symbol will disappear and the LCD will display OH before the device turning off.

If the data transmission fails, an error message will be shown (E6 as an example) on the display for several seconds then the device will turn off.

In the case of a data transmission failure (E5 or E6), up to 60 measurements are saved on the device and will be sent when a successful connection is achieved.

Tip:
You can press “ START/STOP ” button at any time to stop measuring during the process of measurement.

INFORMATION FOR USER

Tips for Measurement

Measurements may be inaccurate if taken in the following circumstances:

• Within an hour a²er dinner or drinking

• A²er drinking tea, coee or using tobacco products.

• Within 20 minutes a²er taking a bath

• While talking, gesturing or while in a loud environment.

• In a very cold environment
  

• When you have to go to the bathroom
  

Maintenance
In order to get the best performance, please follow the instructions below.

• Store device in a dry place away from direct sunlight.

• Keep away from water. If splashed, immediately dry with a clean towel.
  

• Avoid shaking or dropping the device.

• Store device in a place that avoids quick changes in temperature.
  

• When cleaning device, use a lightly moist cloth without soap or detergent.

• Do not wash or immerse the cu in water.

What are systolic pressure and diastolic pressure?

• When ventricles contract and pump blood out of the heart, the blood pressure reaches its maximum value in the cycle, which is called systolic pressure. When the ventricles relax, the blood pressure reaches its minimum value in the cycle, which is called diastolic pressure.
  

What is the standard blood pressure classification?
The chart on the right is the standard blood pressure classification published by American Heart Association (AHA).

This chart reflects blood pressure categories defined by American Heart Association.

Blood Pressure Category| Systolic mmHg upper#)| | Diastolic mmHg (lower#)
Normal| less than 120| and| less than 80
Prehypertension| 120-129| and| less than 80
High Blood Pressure (Hypertension) Stage 1| 130-139| or| 80-89
High Blood Pressure (Hypertension) Stage 1| 140 or higher| or| 90 or higher
Hypertensive Crisis (Consult your doctor immediately)| Higher than 180| and /or| Higher than 120

CAUTION
Please consult a physician if your measuring result falls outside the range. Please note that only a physician can tell whether your blood pressure value has reached a dangerous point.
Irregular Heartbeat Detection
An irregular heartbeat is detected when a heartbeat rhythm varies while the device is measuring systolic pressure and diastolic pressure. During each measurement, blood pressure monitor will keep a record of all the pulse intervals and calculate the average value of them. If there are two or more pulse intervals, the dierence between each interval and the average is more than the average value of ±25% , or there are four or more pulse intervals, the dierence between each interval and the average is more than the average value of ±15%, then the irregular heartbeat symbol will appear on the display with the measurement result.
CAUTION
The appearance of the IHB icon indicates that a pulse irregularity consistent with an irregular heartbeat was detected during measurement. Usually this is NOT a cause for concern. However, if the symbol appears o²en, we recommend you seek medical advice. Please note that the device does not replace a cardiac examination, but serves to detect pulse irregularities at an early stage.
Why does my blood pressure fluctuate throughout the day?

1. Individual blood pressure varies throughout the day. It is also aected by the way you tie your cu and your measurement position. It is important to take measurements in the same conditions.
2. If the person takes medicine, the pressure may vary even more.
3. Wait at least 3 minutes between measurements

What you need to pay attention to when you measure your blood pressure at home:

• If the cu is tied properly.
• If the cu is too tight or too loose.
• If the cu is tied on the upper arm.
• If you feel anxious.
• Taking 2-3 deep breaths before beginning will be better for measuring.

Advice:
Relax yourself for 4-5 minutes prior to taking a measurement.

Why do I get a di erent blood pressure at home compared to the hospital?
The blood pressure is dierent even throughout the day due to weather, emotion, exercise etc.
Also, there is a phenomenon called the “white coat” eect, which means blood pressure usually increases when measured in clinical settings.
Is the result the same if measuring on di erent arms?
It is acceptable to use either arm but results might dier between arms for some people. It is suggested that you measure on the same arm every time.

TROUBLESHOOTING

This section includes a list of error messages and frequently asked questions for problems you may encounter with your blood pressure monitor. If the device is not operating as you think it should, check here before arranging for servicing.

then measure again.
E3 shows| The measurement process does not detect the pulse signal.| Loosen the clothing on the arm and then measure again
E4 shows| The treatment of the measurement failed.| Relax for a moment and then measure again.
E5 shows| Failed to communicate with the server| Contact customer service
E6 shows| Radio communication failure| Contact customer service
EExx,shows on the display.| A calibration error occurred.| Retake the measurement.
If the problem persists, contact the retailer or our customer service department for further assistance.
Refer to the warranty for contact information and return instructions
Warning message| ‘out’ shows| Out of measurement range| Relax for a moment. Refasten the cuff and then measure again. If the problem persists, contact your physician.

SPECIFICATIONS

Power supply| Battery powered mode: 6VDC 4×AA batteries AC adaptor powered mode: 6V 1A (not included) (Please only use the recommended AC adaptor model).
---|---
Display mode| Digital LCD V.A.78mm*92mm
Measurement mode| Oscillography testing mode
Measurement range| Rated cuff pressure: 0mmHg~299mmHg(0kPa ~ 39.9kPa) Measurement pressure:

SYS: 60mmHg~230mmHg (8.0kPa~30.7kPa) DIA: 40mmHg~130mmHg (5.3kPa~17.3kPa)
Pulse value: (40-199)beat/minute

Accuracy| Pressure: 5ºC-40ºCwithin±3mmHg(0.4kPa)  Pulse value:±5%
Normal working condition| A temperature range of : +5°C to +40°CA relative humidity range of 15% to 90%,non-condensing, but not requiring a water vapor partial pressure greater than 50 hPaAn atmospheric pressure range of : 700 hPa to 1060 hPa
Storage &transportation condition| Temperature:- 20°C to +60°CA relative humidity range of ≤ 93%, non-condensing, at a water vapour pressure up to 50hPa
Measurement perimeter of the upper arm| About 22cm~42cm
Weight| Approx.393g(Excluding the batteries)
External dimensions| Approx.154.3mm121.5mm68.1mm
Attachment| 4×AA batteries,user manual
Mode of operation| Continuous operation
Degree of protection| Type BF applied part
Protection against ingress of water| IP21 It means the device could protected against solid foreign objects of 12.5mm and greater, and protect against vertically falling water drops.
Device Classification| Battery Powered Mode: Internally Powered ME Equipment AC Adaptor Powered Mode: Class II ME Equipment
Software Version| A01

Authorized Component
If plug in power functionality is desired, only use a Pylo authorized AC adapter (not included).

Adaptor:
Type: BLJ06L060100P-U
Input: 100-240V 50-60Hz,0.2Amax
Output: 6V 1000mA

Contact Pylo Health
For more information about our products, please visit www.pylo.com. You can get customer service, usual problems and customer download, Pylo will serve you anytime.

Contact Information: Pylo Health 28632 Roadside Drive Suite 215 Agoura Hills, CA 91301  info@pylo.com | 818-600-7162

FCC Statement
contains FCC ID: XMR2020BG95M2
This device complies with Part 15 of the FCC Rules. Operation is subject to the 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.

Caution: The user is cautioned that changes or modifications not expressly approved by the party responsible for compliance could void the user’s authority to operate the equipment.

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 o 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 dierent from that to which the receiver is connected.
• Consult the dealer or an experienced radio/TV technician for help.

FCC Radiation Exposure Statement:
This equipment complies with FCC radiation exposure limits set forth for an uncontrolled environment. This transmitter must not be co-located or operating in conjunction with any other antenna or transmitter.

EMC GUIDANCE

Complied Standards List

Guidance and manufacturer’s declaration – electromagnetic Immunity

|
---|---
Immunity Test| IEC 60601-1-2 Test level| Compliance level|
Electrostatic discharge (ESD)

IEC 61000-4-2

| ±8 kV contact

±2 kV, ±4kV, ±8 kV, ±15 kV air

| ±8 kV contact

±2 kV, ±4kV, ±8 kV,

±15 kV air

|
Electrical fast transient/ burst

IEC 61000-4-4

| ±2 kV for power supply lines

±1 kV signal input/output 100 kHz repetition frequency

| ±2 kV for power supply lines

±1 kV signal input/output 100 kHz repetition frequency

|
Surge IEC61000-4-5| ±0.5 kV, ±1 kV differential mode

±0.5 kV, ±1 kV,±2 kV common mode

| ±0.5 kV, ±1 kV differential mode

±0.5 kV, ±1 kV,±2 kV common mode

|
Voltage dips, short interruptions and voltage variations on power supply input lines

IEC 61000-4-11

| 0 % UT; 0,5 cycle. At 0°, 45°, 90°, 135°,

180°, 225°, 270° and 315°.0 % UT;

1 cycle and 70 % UT; 25/30 cycles; Single phase: at 0°.0 % UT; 250/300 cycle

| 0 % UT; 0,5 cycle. At 0°, 45°, 90°, 135°,

180°, 225°, 270° and 315°. 0 % UT;

1 cycle and 70 % UT; 25/30 cycles; Single phase: at 0°. 0 % UT; 250/300 cycle

|
Power frequency magnetic field IEC 61000-4-8| 30 A/m

50Hz/60Hz

| 30 A/m

50Hz/60Hz

|
Conduced RF IEC61000-4-6| 3 V

0,15 MHz – 80 MHz

6 V in ISM and amateur radio bands between 0,15 MHz and 80 MHz

80 % AM at 1 kHz

| 3 V

0,15 MHz – 80 MHz

6 V in ISM and amateur radio bands between 0,15 MHz and 80 MHz

80 % AM at 1 kHz

|
Radiated RF IEC61000-4-3| 10 V/m

80 MHz – 2,7 GHz

80 % AM at 1 kHz

| 10 V/m

80 MHz – 2,7 GHz

80 % AM at 1 kHz

|
NOTE UT is the a.c. mains voltage prior to application of the test level.|
Emissions| Compliance|
RF emissions CISPR 11| Group 1|
RF emissions CISPR 11| Class [ B ]|
Harmonic emissions IEC 61000-3-2| Class A|
Voltage fluctuations/ flicker emissions

IEC 61000-3-3

| Comply|
Radiated RF

IEC61000-4-3

(Test

specifications

for

ENCLOSURE

PORT

IMMUNITY to

RF wireless

commu-

nications

equipment)

| Test

Frequency

(MHz)

| Band

(MHz)

| Service| Modulation| Modulation

(W)

| Distance (m)

0.3

| IMMUNITY

TEST

LEVEL

(V/m)

|

 |  |  |  |  |  |
385| 380-

390

| TETRA

400

| Pulse

modulation

b) 18Hz

| 1.8| 27|
 |  |  |
450| 430-

470

| GMRS 460,

FRS 460

|  |  |  |  |
FM c) ±

5kHz

deviation

1kHz sine

| 2| 0.3| 28|
 |
 |  |
710| 704-

787

| LTE Band

13, 17

| Pulse

modulation

b) 217Hz

| 0.2| 0.3| 9|
745
780
810| 800-

960

| GSM

800/900,

TETRA 800,

iDEN 820,

CDMA 850,

LTE Band 5

| Pulse

modulation

b) 18Hz

| 2| 0.3| 28|
870
930
1720| 1700-| GSM 1800;| Pulse| 2| 0.3| 28|
1990| CDMA| modulation|  |
1845
 | 1900;| b) 217Hz|  |
 | GSM 1900;

DECT;

|  |  |
1970
 |  | LTE|  |  |
 |  | Band 1,|  |  |
 |  | 3, 4,25;|  |  |
 |  | UMTS|  |  |
2450| 2400-

2570

| Bluetooth, WLAN,

802.11

b/g/n,

RFID

2450, LTE

Band 7

| Pulse modulation

217 Hz

| 2| 0.3| 28|
5240| 5100-| WLAN

802.11

a/n

| Pulse

modulation 217 Hz

| 0.2| 0.3| 9|
5800
5500
5785|  |

References

• Pylo Health – Connected Health Made Easy

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