INN-015 - Pressure gauge Innoliving - Free user manual and instructions

USER MANUAL INN-015 Innoliving

Simple gray rectangular bar with vertical lines at both ends, no text or symbols present

INN-015 MISURATORE DI PRESSIONE DIGITALE DA POLSO

|

MANUALE D'ISTRUZIONE

Simple line drawing of a cylindrical device with attached wires and a curved arrow indicating direction (no text or symbols)

Diagram showing two steps of battery charging process: one with battery and cable, the other with battery and cable.

1

NOTA:

Line drawing of a human forearm with a hand pointing to the wrist area, showing a curved arrow indicating motion (no text or symbols)

✗ Too Low ✗ Too High OK

Thank you for purchasing the upper arm digital pressure monitor INN-015.

For a proper use of the product, please read the following instructions carefully before use and consult your physician if you have any queries about your blood pressure.

This fully automatic tool uses the oscillometric non-invasive method, which detects blood pressure and heart rate through the brachial artery, the result is shown on the display. Without the use of a stethoscope, it is still possible to obtain a blood pressure reading in an easy and fast way.

HOW TO USE

This device is intended for use by professional medical personnel and home users. It was designed to measure the systolic and diastolic pressure of the blood of an adult individual using a non-invasive technique, by means of an inflatable cuff worn in the upper arm.

WARNING/CAUTION: Indicates a dangerous situation which, if not could result in death or serious injury.

WARNING:

• Consult your physician before starting to measure your blood pressure.
• Like any oscillometric blood pressure measurement, some medical conditions can affect the measurement accuracy, among others:
• Kidney problems
• Disorder of the cardiac rhythm
• Very low blood pressure
• Very low blood perfusion

GB

• Patients in shocks
• Diabetes
• Vessel anomalies
• People with electrical implants such as a cardiac pacemaker
• Women who are pregnant
• Patient who are pre-eclamptic
• Patient motion during measurement

These conditions can lead to incorrect readings. This represents a risk for your health, since values may be interpreted incorrectly. Always consult your physician to evaluate your state of health in a suitable way.

IMPORTANT SAFETY INSTRUCTIONS

- This product is not intended to provide a medical diagnosis. Measurement results are for reference only. Self-diagnosis and treatment, e.g. regarding medication, using measured results represents risk

for your health. Always consult with a licensed physician for determination of appropriate medication and

dosage thereof. Follow the instructions of your physician or licensed healthcare provider.

- Please, consider that tolerances in measurements are admitted. See "TECHNICAL SPECIFICATIONS".

• Measure the pressure with any cuff repeatedly can cause:

- A nerve compression with temporary wrist/ hand paralysis

- The release of an arterial or venous thrombus, which can cause a life threatening situation.

Please contact your physician about the specific risks of cuff pressure in your specific case.

GB

• The "irregular heartbeat" function does not replace a cardiac examination, but can help detect a potential irregularity of the heartbeat. Always consult your doctor to evaluate your state of health.
• The "irregular heartbeat" function is not designed for diagnosing or treating an arrhythmic disorder. Arrhythmia can only be ascertained by a licensed physician.
• The "WHO BLOOD PRESSURE CLASSIFICATION" chart is not intended to replace a medical diagnosis. This chart is only for reference for different classifications of blood pressure.
• If you notice abnormal or suspicious variations in blood pressure measurements, consult your physician immediately.
• Women who underwent a breast or axillaries lymph node removal operation should consult a physician or licensed healthcare provider before starting blood pressure measurements.
• This device must be used in accordance to the specified ambient conditions, otherwise the accuracy of readings might be affected. See "TECHNICAL SPECIFICATION" for details.
• Do not wrap the cuff around body parts other than your upper left arm. Misuse represents a risk to your health.
• This product is not intended for use by or on children, infants or on persons who cannot express their consent, e.g. persons with mental disorders or similar. Consult your physician for alternative methods of measuring a child's blood pressure.
• Packaging materials are a deadly hazard for children and can cause suffocation. Remove all packaging materials immediately and keep them away from children at all times.
• This product contains small parts that may present a choking hazard to children. Keep the unit and all parts out of reach of children.

GB

• Proper cuff size is important for accurate measurements. Only use the device on adults who have the right upper arm circumference for this instrument. See section "Technical Specifications" for suitable arm circumferences.
• Electromagnetic interference: Avoid strong electrical or electromagnetic fields in the direct vicinity of the device (e.g. mobile telephones, microwave ovens) while it is in operation, as inaccurate measurements may result. To prevent such interference, use the unit at a sufficient distance from such devices or turn the devices off.
• Batteries should not be charged or reactivated by any other means. The batteries may explode.
• Keep the batteries away from fire as there is a risk of ignition or explosion.
• In case battery fluid leaks and come into contact with your eyes or skin, do not rub and immediately rinse with plenty of clean water and seek medical advice..
• Do not use the equipment where flammable gas (e.g. anaesthetics gas, oxygen or hydrogen) or flammable liquid (e.g. alcohol) are present.
• Do not use any cuffs and accessories other than those recommended by the manufacturer for use with this product. Cuffs and accessories not approved for use with this device may cause damage to your health and to the product.
• The tubing presents a strangulation hazard. Keep this product away from children and those who require close supervision, e.g. people with mental disorders.

CAUTION

- The device should not be used when your arm has been wounded/injured or when a catheter has been inserted. Such use may result in injury.

• Remove any kind of upper arm jewelry or similar before taking a measurement. This could cause bruises.
• Do not place the arm cuff over heavy clothing (e.g. a jacket or sweater sleeve) as the blood pressure monitor will not be able to take a proper measurement and there is an elevated danger of acquiring hematoma or skin marks during the course of the measurement.
• In case the cuff does not stop inflating, interrupt the measurement by pressing the ON/OFF button and open the cuff at once.
• If a battery has leaked do not touch the battery fluid. Avoid skin contact (e.g. put on protective gloves) and clean the battery compartment with a dry cloth.
• Do not disassemble the unit, it may result in injuries.
• When applying the arm cuff, make sure there are no wrinkles in the cuff. This could cause bruises.
• Blood pressure measurements can lead to temporary marks on the skin at the site of the cuff placement. This is especially the case in high repetition rates, in hypertonic patients and in patients with weak heart rates. In rare cases a mark may persist for a couple of days. Please contact your physician about these specific risks of cuff pressure in your specific case.

MAINTENANCE

- The blood pressure monitor is composed by precision electronic components, the accuracy of readings and the instrument's operating life depend on a careful maintenance and care of the product. Protect the unit against hard knocks (e.g. dropping the unit), moisture, water, dirt, dust, chemicals, extreme hot or cold temperatures, major temperature fluctuations, direct exposure to sunlight and heat sources which are too

GB

close (e.g. stoves, heating radiators). This may damage the unit. The device must be stored in the specified ambient conditions. Please see section "Technical Specification" for details.

• The device is designed and manufactured for a long service life. However it is generally recommended to have the monitor inspection every 2 years to ensure proper functioning and accuracy.
• Never immerse and/or spill water or any other liquid onto the monitor or any components, otherwise liquid may enter it and cause damages.
• Never use rechargeable batteries. This may damage the unit.
• Replace all batteries at the same time and use batteries of the same type. Do not mix old and new batteries.
• Never try to repair, open and/or disassemble the unit or adjust it yourself. This may cause damage to the unit and impair functions. If you cannot fix the problem using the "TROUBLESHOOTING" instructions, contact the authorized after sales service.
• Do not drop or insert any object into any openings or hoses. This may damage the unit.
• Do not press the buttons with excessive force or with pointed objects.
• Clean your device and cuff carefully with a soft damp cloth and dry it immediately with a soft dry cloth. Do not press.
• Do not use any aggressive solvents, cleaning agents, detergents or any other strong chemicals (e.g. thinner, alcohol, benzene) to clean the device.
• When storing the device, make sure that no heavy objects are placed on top of it.
• Do not fold the cuff and tubing tightly. The cuff tube should not have any sharp kinks and keep it away from sharp edges.
• Leaking batteries may damage the unit. If you do not intend to use the unit for long periods, remove the batteries from the battery compartment before storing the device

PRODUCT DESCRIPTION AND DISPLAY READING

Display Time Memory User Cuff Start/Stop Battery Cover

GB

Average of previous measurement memory Date Time User 1 User 2 30/88 30/88 30/88 AM PM 1 AVG 2:88 Systolic Pressure Grave Hypertension Moderate Hypertension Mild Hypertension High Hypertension Normal Optimal Heartbeat indicator Battery indicator Irregular heartbeat indicator Pulse rate Release air

INSERT/CHANGE THE BATTERIES

1. Remove the battery cover on the bottom of the unit as shown in the figure below.

2. Remove the old batteries and insert new ones. Use LR03 or AAA alkaline batteries and use only batteries of the same type.

3. Make sure that the battery polarity (+) and (-) correspond to those indicated in the battery compartment.

4. Replace the battery cover

GB

NOTE:

• Insert the batteries as shown in the battery compartment. If not, the device will not work or even be damaged.
• The icon [7] indicates battery power is enough.
• When battery power becomes weak, the icon [☐] and "E6" appear in the display, replace all batteries with new ones. Do not mix old and new batteries.
• Never use rechargeable batteries. This may damage the unit.
• Battery life may vary with ambient temperature and may be shorter at low temperature.

Memory function:

• Normal measurement with salvage values of user [1] or [2] :
• Press the button with the symbol of the user to select user [1] or [2]. The measurement values are stored in the user selected.
  • Data Storage: to consult the data stored
• Select user [1] or [2] by pressing the button with user symbol. To consult the memories press M.

HOW TO SET THE CLOCK

24h co is

1

3

3

3

3

When new batteries are installed

1. "24h" will flash on display automatically.
2. Press M to select 24h or 12h.
3. Press [⑨] button to confirm and "YEAR" will appear on the display.
4. Press M to select current YEAR.
5. Press [💡] button to confirm and "MONTH" will appear on the display.
6. Press M to select current Month.
7. Press [icon] button to confirm and "DAY" will appear on the display.
8. Press M to select current day.
9. Press [💡] button to confirm and "HOUR" will appear on the display.
10. Press M to select current hour.
11. Press [💡] button to confirm and "MINUTE" will appear on the display.
12. Press M to select current minute.
13. Press [💡] to confirm and switch the device off.

GB

AT ANY TIME YOU CAN SET THE DATE AND TIME:

1. Press the button [💡], to display date and time. Press and hold button [💡] for 3 seconds and "24h" will flash to indicate that you are in the settings section, follow the procedure as explained above.

HOW TO APPLY THE CUFF

1. Bare your left wrist, making sure that the circulation in the arm is not restricted by any cloth etc. that are too tight. Position the cuff on the inside of your wrist.

Line drawing of a human arm with a curved arrow indicating motion (no text or symbols)

1. Fasten the cuff with the velcro, fastening so that te upper edge of the monitor is positioned approximately 1 cm below the ball of your thumb.

1cm

1. The cuff has to be fitted tightly around the wrist but should not constrict it.

BEFORE MEASURING BLOOD PRESSURE

1. Apply the arm cuff following the instruction.
2. It is important to rest at least for 5 minutes before each measurement. Otherwise there may be erroneous results.
3. Sit down in a comfortable position, do not cross your legs, your feet should be fit on the floor and your back should be supported by a chair. At the same time your arm should be supported on a flat surface which the cuff is on a level with your heart.
4. Relax your arm and turn your palm upward.
5. Relax, keep still and do not talk during the measurement in order not to distort the result.

NOTE:

• This instrument is intended for use by adult only. Do not use this device on or children, toddlers and infants.
• For reliable monitoring and reference of blood pressure, it is recommended to do the measurement daily at the same time.
• In order to obtain a correct measuring of blood pressure, do not eat, drink alcohol and beverages with caffeine, smoke, exercise or bath for at least 30 minutes before taking a measurement since your blood pressure varies from time to time depending on what you have eaten, drunk and what you have done.

GB

•To minimize measurement variations due to physical activity, relax for five to ten minutes before taking a measurement. If you are excited by emotional stress or muscular movement, the measurement result given out may be inaccurate. Stress raises blood pressure.
- You should not be physically tired or exhausted while taking measurement.
- Perform measurements in a quiet and relaxed environment at room temperature.
- Remain relax, still and do not talk during measurement since the accuracy of any blood pressure
measurement with this device can be affected by those multitude of causes.
• Always wait at least 5 minutes between measurements to allow the blood circulation in your arm to return normal. You may need to increase the wait time depending on your individual physiological characteristic.
- If the device detect an abnormal condition, measurement stops and an error code will appear on the display. See "TROUBLESHOOTING" for more details.
- This device focus its measurements on your heartbeat. If you have a very weak or an irregular heartbeat, the device may have difficulty in determining your blood pressure. (An irregular heartbeat is defined as a heartbeat that varies by 25% from the average of all heartbeats during measurement.)
- Do not apply any kind of pressure on the hose during measurement, e.g. laying your arms or any other object on the hose. This could cause incorrect measurements

MEASURE YOUR BLOOD PRESSURE

23/2 1930 0 23/2 1930 62 23/2 1930 160 23/2 1930 120 83 86

1. Follow the instruction to make yourself ready.
2. Press [①] to start measurement.
3. The cuff starts to inflate. It is normal for the cuff to feel very tight. A pressure bar indicator is displayed during measurement. See "PRESSURE BAR INDICATOR" for more details
4. Once the pulse is detected, the symbol ♥ will flash according to your pulse beat.
5. When the measurement is complete, the systolic and diastolic pressure and pulse rate are displayed and stored. At the same time, the cuff expels the remaining air and deflates completely
6. Press [①] to switch the device off.

NOTE:

You can stop inflation by pressing M button at any time

GB

PRESSURE BAR INDICATOR

The standards for assessing high blood pressure, regardless of age, have been established by the WHO (World Health Organization - WHO), as shown in the chart below:

Reference Material: Journal of Hypertension 1999, Vol 17 No.2

WHO CLASSIFICATION INDICATOR

Each of the segments of the bar indicator corresponds to the WHO blood pressure classification.

Grave Hypertension Moderate Hypertension Mild Hypertension Normally High Normal Optimal

GB

SEE AVERAGE AND PREVIOUS MEASUREMENT DATA

This device can store the measurement readings for each user. Every time you complete the measurement, the device automatically stores the measurement result.

1. To get the average measurement data of the last 3 measurements, press to select user 1 or 2.
2. Press M to see the average measurement data.
3. Press again M to see the previous measurements.
4. Press Ⓐ to switch the device off.

DELETE MEASUREMENT DATA

This device has two data erasure methods

(A) Delete a single measurement

1. Select the recording you want to delete
2. Press and hold [+/M] until you will see "CL" and "-" on the display.
3. Press [💡] to confirm and the display will show "CL" e "00"

(B) To delete all previous measurements

1. Press [+M] to see the average of the previous measurement
2. Press and hold [+/M] until "CL" and "--" Will apprar on the display
3. Press [💡] to confirm and the display will show "CL" and "00"

24h 20:15 2.1 000 6/3 3:38 6/3 000 6/3 000

IRREGULAR HEARTBEAT

This blood pressure monitor provides a blood pressure and pulse rate measurement even when an irregular

heartbeat occurs. An irregular heartbeat is defined as a heartbeat that that varies by 25% from the average of all heartbeats during the blood pressure measurement. It is important that you are relaxed, remain still and do not talk during measurements.

NOTE:

• It is advisable to contact your physician if you see this [♥] indicator frequently.
• The "irregular heartbeat" function does not replace a cardiac examination, but it may help to detect potential heart rate irregularities at an early stage. Always consult your physician to determine what will be suitable for you.
• The "irregular heartbeat" function is not designed for diagnosing or treating an arrhythmic disorder. Arrhythmia can only be determined by a licensed physician.

BLOOD PRESSURE

What is Blood Pressure?

Blood pressure is the force exerted by blood against the walls of the arteries. Systolic pressure occurs when the heart contracts. Diastolic pressure occurs when the heart expands. Blood pressure is measured in millimeters of mercury (mmHg). One's natural blood pressure is represented by the fundamental pressure, which is first measured in the morning while one is still at rest and before eating.

GB

What is hypertension and how is it controlled?

Hypertension is an abnormally high arterial blood pressure. If left unattended, hypertension can cause many health problems including stroke and heart attack. Hypertension can be controlled by altering one's lifestyle, avoiding stress, and with medication under a doctor's supervision. To prevent hypertension or to keep it under control:

• Do not smoke
  • Exercise regularly
• Reduce salt and fat intake
  • Have regular physical checkups
• Maintain proper weight

Why measure blood pressure at home?

Blood pressure measured at a clinic or doctor's office may cause apprehension or fear and can produce an elevated reading, 25 to 30mmHg higher than that measured at home. Home measurement reduces the effects of outside influences on blood pressure readings, supplements the doctor's readings and provides a more accurate, complete blood pressure history.

TROUBLESHOOTING

Nothing appears in the display, even when the power is turned on.	Batteries are drained Repiece all Batteries with new ones
	Battery polarities are not in the correct position.	Re-install the batteries with their negative and positive ends matching their indicated in the battery compartment. larità indicate.
ERROR code 1 (E1) appears on the display	The cuff position is not fastened properly	Apply the cuff correctly
	The cuff position is not correct	Sit comfortably and still. Ensure that the cuff is the same level as the heart

GB

ERROR code 2 (E2) appears on the display	You moved your arm or body during measurement	Make sure you remain very still and quiet during the measurement
ERROR code 3 (E3) The cuff	may not be applied correctly	Check whether tube connection of the cuff is secured to the unit properly
ERROR code 4 (E4)	The unit does not measure	If you have a very weak or irregular heartbeat, the device may have difficultly in determining your blood pressure
	There is a measuring error $it comfortably and still.Fasten the cuff again carefully
ERROR code 5 (E5) Cuff over	inflated The measurement range	is over 300 mmHg.It is recommended to see doctor as soon as possible.
ERROR code 6 (E6) Low battery Replace Batteries
The cuff keeps reinflating Circuit blocked Remove and reinsert the batteriesand then proceed to take measurement again.

GB

TECHNICAL SPECIFICATION

Display: LCD
Range di misurazione	Systolic Pressure: 50-250 mmHg;Diastolic Pressure: 30-200 mmHg
Pulse rate 40-180 beats / min
Accuracy	Pressure: +/-3 mmHg Pulse: +/-5%
Resolution	Pressure: 1 mmHg Pulse: 1 battito/minuto
Measuring Method Non-invasive, Oscillometric method
Power supply 2 x 1.5V AAA batterie s
Operating Temperature / Humidity +5°C a	+40°C, 15-93% RH max
Storage Temperature / Humidity 25°C a	+70°C, up tp 93% RH max
atmospheric pressure 700hPa to 1060hPa
External dimension About 84 x 77 x 15mm
Wrist circumference 13.5 - 23cm
Accessories	Cuff, Instruction Manual, Batteries, Storage Pouch
Classification Application part Type BF BF

SYMBOL

Symbol	Meaning
	Lot number
	Type BF: Device, cuff and tubing are designed to provide special protection against electrical shocks
DIA	Diastolic Blood Pressure in mmHg
PUL Beats
	EC Directive Medical Device Label
	Caution
	WEEE Label
	Read carefully the user manual
IP22 Protection Level

GB

NOTICE : Operation mode : Continuous

INFORMATION TO USERS according to Legislative Decree No. 49 of March 14, 2014 "2012/19/UE Implementation of the Directive on Waste Electrical and Electronic Equipment (WEEE)"

The crossed-out dustbin symbol indicates that the product at the end of its life must be collected separately from other waste. The user should, therefore, take the equipment with the essential components at the end of its useful life to the separate collection center of electronic and electrical waste, or return it to the retailer when purchasing new equipment of equivalent type, in ratio of one to one, or one to zero for devices with larger side less than 25 CM. The separate collection for the decommissioned equipment for recycling, treatment and environmentally compatible disposal contributes to avoid possible negative effects on the environment and human health and promotes recycling of the materials. Improper disposal of the product by the user entails the application of administrative sanctions according to Legislative Decree No. 49 of 14 March 2014

The batteries used in this device must be disposed of in the special bins at the end of their life. Please inform yourself about the local rules on separate collection batteries. The correct disposal of batteries helps preventing potentially negative consequences on the environment.

EMC GUIDANCE

Guidance and manufacturer's declarations – electromagnetic emissions

INN-015 requires special precautions regarding EMC and must be installed and put into service according to the EMC information contained in this user manual;

Portable and mobile radiocommunication equipment may affect the operation of INN-015;

The appliance or system must not be used near other appliances and, if it is necessary to use it near other appliances, the electro-medical device must be observed to check normal functioning in the configuration in which it is used.

The electro-medical device has been tested and found to comply with the emission and immunity limits of electromedical equipment according to IEC60601-1-2: 2014. These limits are designed to provide adequate protection against harmful interference in a typical medical installation. However, there is no guarantee that interference will not occur in a particular installation. If the electro-medical device, interacting with another device, causes or receives detectable interference, the user is invited to limit interference by adopting one or more of the following measures:

1. reorient or relocate the receiving device;
2. increase the distance between the appliances;
3. contact the manufacturer or local technician for assistance.

GB

Guidance and declaration of manufacturer – electromagnetic emmissions
INN-015 is intended to be used in the electromagnetic environment specified below. The customer or user of device must assure it's used in this environment.
Emissions tests Compliance Electromagnetic environment
Emissions at RF CISPR 11 Group 1		INN-015 uses RF energy only for its internal operation. As a result, RF emissions are very low and are unlikely to cause any interference in nearby electronic devices
CISPR 11 emissions Class B INN-015 is suitable for use in		all environments, including domestic and those directly connected o a public low-voltage power supply, that supplies buildings used for domestic purposes.
IEC 61000-3-2 harmonic emissions	Not applicable
Voltage fluctuations emissions/flicker IEC 61000-3-3	Not applicable

Guidance and declaration of manufacturer – electromagnetic immunity
IINN-015 is intended to be used in the electromagnetic environment specified below. The customer of user of INN-015 must assure it's used in this environment
Immunity test IEC	60601 test level Compliance level Electromagnetic environment
Electrostatic discharge (ESD) IEC 61000-4-2	+- 8 kV contact +- 8 kV contact		Floors must be made of wood, concrete or ceramic tiles. If the floors are covered with synthetic material, the relative humidity should be at least 30%
	+- 2; 4; 8; 15 kV air	+- 2; 4; 8; 15 kV air
Campo magnetico ad alta frequenza (50/60Hz) IEC 61000-4-8	30 A/m 30 A/m		Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment.

GB

Guidance and declaration of manufacturer – electromagnetic immunity
INN-015 is intended to be used in the electromagnetic environment specified below. The customer of user of INN-015 must assure it's used in this environment Portable and mobile RF communications equipment should be used no closer to any part of the blood pressure monitor including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter
Immunity test IEC 60601 test level Compliance			level	Recommended separation distance d:
RF IrradiateIEC 61000-4-3	3 V/m e 10 V/mda 80 MHz a 2,7 GHz		3 V/m e 10V/m	d = 30 cm
IEC 61000-4-3Proximity fieldimmunity fromwireless RFcommunicationdevices	TETRA 400380 – 390 MHz	27 V/m 27 V/m		d = 30 cm
	GMRS 460FRS 460430 – 170 MHz	28 V/m 28 V/m
	LTE Band 13, 17704 – 787 MHz	9 V/m 9 V/m
	GSM 800/900, TETRA800, iDEN 820, CDMA850, LTE Band 5800 960 MHz	28 V/m 28 V/m

GB

IEC 61000-4-3 Proximity field immunity from wireless RF communication devices	GSM 1800; CDMA 1900; GSM 1900; DECT; LTE Band 5 1700 – 1990 MHz	28 V/m 28 V/m	d= 30 cm
	Bluetooth, WLAN, 802.11 b/g/n, RIFD 2450, LTE Band 70 2400 – 2570 MHz	28 V/m 28 V/m
	WLAN 802.11 a/n 5100 – 5800 MHz	9 V/m 9 V/m

GB

REMARKS

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 hwristful 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 hwristful interference to radio communications. However, there is no guarantee that interference will not occur in a particular installation. If this equipment does cause hwristful 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 technician for help.

WARNING

- To comply with the limits of the Class B digital device, pursuant to Part 15 of the FCC Rules, this device is

comply with Class B limits. All peripherals must be shielded and grounded. Operation with non-certified

peripherals or non-shielded cables may results in interference to radio or reception.

- Any changes or modifications not expressly approved by the grantee of this device could void the user's authority to operate the device.

Pure horizontal bar with vertical lines and a small square marker at the bottom (no text or symbols)

innoliving

Innoliving Spa Via Merloni, 2/B 60131 Ancona Italy Tel [phone] www.innoliving.it

MADE IN CHINA

CE 1936

Rev.05_07.2021