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Gima S.p.A.
Via Marconi, 1 - 20060 Gessate (MI) Italy
gima@gimaitaly.com - export@gimaitaly.com
PROFESSIONAL MEDICAL PRODUCTS
www.gimaitaly.com
WRIST AUTOMATIC
BLOOD PRESSURE MONITOR
Operation Guide
ATTENTION:
The operators must carefully read
and completely understand the present manual
before using the product.
SPECIFICATIONS
1. Product name: Blood Pressure Monitor
2. Model: KD-735
3. Classication: Internally powered, Type BF applied part, IP22, No AP or APG,
Continuous operation.
4. Machine size: Approx. 85mm x 64.5mm x28mm
(3 11/32” x 2 17/32” x 1 3/32”)
5. Cuff circumference:14cm - 19.5cm (5 1/2” - 7 11/16”)
6. Weight: Approx. 110g (3 7/8 oz.) (exclude batteries)
7. Measuring method: Oscillometric method, automatic ination and measurement
8. Memory volume: 2x 60 times with time and date stamp
9. Power source: batteries: 2 ×1.5V SIZE AAA
10. Measurement range:
Cuff pressure: 0-300 mmHg
Systolic: 60-260 mmHg
Diastolic: 40-199 mmHg
Pulse rate: 40-180 beats/minute
11. Accuracy:
Pressure: ±3mmHg
Pulse rate: Less than 60: ±3bpm
More than 60 (incl.): ±5%
12. Environmental temperature for operation: 5°C~40°C (41°F~104°F)
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SETUP AND OPERATING PROCEDURES
1. Battery loading
a. Open battery cover at the back of the monitor.
b. Load two “AAA” size batteries. Please pay attention to polarity.
c. Close the battery cover.
When LCD shows battery symbol , replace all batteries
with new ones.
Rechargeable batteries are not suitable for this monitor.
Remove the batteries if the monitor will not be used for a
month or more to avoid relevant damage of battery leakage.
Avoid the battery uid to get in your eyes. If it
should get in your eyes, immediately rinse with
plenty of clean water and contact a physician.
The negative terminal of the battery needs to be compressed into the battery compartment properly after horizontal compression of the negative
electrode. The battery is in contact with the spring.
Make sure the battery cover is intact and not damaged before installing
the battery
The monitor, the batteries and the cuff, must be disposed of according to
local regulations at the end of their usage.
Battery
INDEX
IMPORTANT INFORMATION ...........................................................................3
CONTENTS AND DISPLAY INDICATORS .......................................................4
INTENDED USE ............................................................................................... 5
PACKAGE CONTENTS ...................................................................................5
CONTRAINDICATION ......................................................................................5
PRODUCT DESCRIPTION...............................................................................6
SPECIFICATIONS ............................................................................................7
NOTICE ...........................................................................................................8
SETUP AND OPERATING PROCEDURES ....................................................13
1. Battery loading .......................................................................................... 13
2. Clock and date adjustment ....................................................................... 14
3. Connecting the cuff to the monitor ...........................................................15
4. Applying the cuff .......................................................................................15
5. Body posture during measurement ...........................................................16
6. Taking your blood pressure reading ..........................................................17
7. Displaying stored results ...........................................................................18
8. Deleting measurements from the memory ................................................20
9. Assessing high blood pressure for adults .................................................20
10. Technical alarm description ..................................................................... 21
11. Troubleshooting (1) .................................................................................. 22
12. Troubleshooting (2) .................................................................................. 23
MAINTENANCE ............................................................................................. 25
EXPLANATION OF SYMBOLS ON UNIT .......................................................27
ELECTROMAGNETIC COMPATIBILITY INFORMATION ............................... 29
WARRANTY INFORMATION ......................................................................... 33
IMPORTANT INFORMATION
Normal blood pressure uctuation
All physical activity, excitement, stress, eating, drinking, smoking, body posture
and many other activities or factors (including taking a blood pressure measurement) will inuence blood pressure value. Because of this, it is mostly unusual to
obtain identical multiple blood pressure readings.
Blood pressure uctuates continually ----- day and night. The highest value usually appears in the daytime and lowest one usually at midnight. Typically, the
value begins to increase at around 3:00AM, and reaches to highest level in the
daytime while most people are awake and active.
Considering the above information, it is recommended that you measure your
blood pressure at approximately the same time each day.
Too frequent measurements may cause injury due to blood ow interference,
please always relax a minimum of 1 to 1.5 minutes between measurements to allow the blood circulation in your arm to recover. It is rare that you obtain identical
blood pressure readings each time.
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13. Environmental humidity for operation: ≤90%RH
14. Environmental temperature for storage and transport:
-20°C~55°C (-4°F~131°F)
15. Environmental humidity for storage and transport: ≤90% RH
16. Environmental pressure: 80kPa-105kPa
17. Battery life: Approx 270 times
18. All components belonging to the pressure measuring system, including accessories: Pump,Valve, LCD, Cuff, Sensor
Note: These specications are subject to change without notice.
NOTICE
1. Read all of the information in the operation guide and any other literature in
the box before operating the unit.
2. Stay still, calm and rest for 5 minutes before blood pressure measurement.
3. The cuff should be placed at the same level as your heart.
4. During measurement, neither speak nor move your body and arm.
5. Measuring on same wrist for each measurement.
6. Please always relax at least 1 or 1.5 minutes between measurements to allow
the blood circulation in your arm to recover. Prolonged over-ination (cuff
pressure exceed 300 mmHg or maintained above 15 mmHg for longer than
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3 minutes) of the bladder may cause ecchymoma of your wrist.
7. Consult your physician if you have any doubt about below cases:
1) The application of the cuff over a wound or inammation diseases;
2) The application of the cuff on any limb where intravascular access
or therapy, or an arterio-venous (A-V) shunt, is present;
3) The application of the cuff on the arm on the side of a mastectomy;
4) Simultaneously used with other monitoring medical equipments
on the same limb;
5) Need to check the blood circulation of the user.
8. This Electronic Sphygmomanometers is designed for adults and
should never be used on infants or young children. Consult your physician or other health care professionals before use on older children.
9. Do not use this unit in a moving vehicle, This may result in erroneous measurement.
10. Blood pressure measurements determined by this monitor are equivalent to
those obtained by a trained observer using the cuff/stethoscope auscultation
method, within the limits prescribed by the American National Standard Institute, Electronic or automated sphygmomanometers.
11. Information regarding potential electromagnetic or other interference between the blood pressure monitor and other devices together with advice regarding avoidance of such interference please see part ELECTROMAGNETIC COMPATIBILITY INFORMATION. It is suggested that the blood pressure
monitor be kept at least 30 cm away from other wireless devices, such as
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2. Clock and date adjustment
a. Once you install the battery or turn off the monitor, it will enter Clock Mode,
and LCD will display time and date by turns. See picture 2&2-1.
Picture 2 Picture 2-1 Picture 2-2
b. While the monitor is in Clock Mode, pressing both the “START” and “MEM”
button simultaneously, a beep is heard and the month will blink at rst.
See picture 2-2. Press the button “START” repeatedly, the day, hour and min-
ute will blink in turn. While the number is blinking, press the button “MEM” to
increase the number. Keep on pressing the button “MEM”, the number will
increase fast.
c. You can turn off the monitor by pressing “START” button when the minute is
blinking, then the time and date is conrmed.
d. The monitor will turn off automatically after 1 minute of no operation, with the
time and date unchanged.
e. Once you change the batteries, you should readjust the time and date.
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3. Connecting the cuff to the monitor
The cuff is attached to the monitor when it
is packaged. Should the cuff become unattached, align the two plugs and four brackets
of the cuff with the plug sockets and bracket
sockets of the monitor and press the cuff to
the monitor until the plugs and brackets are
securely attached.
4. Applying the cuff
a. Place the cuff around a bare wrist 1-2cm above the
wrist joint on the palm side of the wrist.
b. While seated, place the arm with the cuffed wrist in
front of your body on a desk or table with the palm
up.
If the cuff is correctly placed, you can read the LCD
display.
c. The cuff must be neither too tight nor too loose.
d. You can also take a measurement on your right
wrist as the picture
CONTENTS AND DISPLAY INDICATORS
LCD Display
Blood pressure level
Classication
indicator
Cuff
Memory indicator Date/Time display
Low battery indicator
Blood pressure level
Classication indicator
Irregular heartbeat symbol
Ready to initiate indicator
Note: The pictures in the manual are for reference only.
MEM botton
START botton
Systolic pressure
Diastolic pressure
Pulse rate display
(alternating)
INTENDED USE
Fully Automatic Electronic Blood Pressure Monitor is for use by medical
professionals or at home and is a non-invasive blood pressure measurement
system intended to measure the diastolic and systolic blood pressures and pulse
rate of an adult individual by using a non-invasive technique in which
an inatable cuff is wrapped around the wrist. The cuff circumference is limited
to 14cm-19.5cm (approx. 5 1/2”-7 11/16”).
PACKAGE CONTENTS
• 1 Blood Pressure Monitor With Attached Wrist Cuff
• 1 Operation Guide
• 1 Plastic Bag
CONTRAINDICATION
It is inappropriate for people with serious arrhythmia to use
this Electronic Sphygmomanometer.
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WLAN unit, microwave oven, etc. It can’t be used near active HF SURGICAL
EQUIPMENT and the RF shielded room of an ME SYSTEM for magneticresonance imaging, where the intensity of EM DISTURBANCES is high.
12. If Irregular Heartbeat (IHB) brought by common arrhythmias is detected in the
procedure of blood pressure measurement, a signal of `( )´
Under this condition, the Electronic Sphygmomanometers can keep function, but the results may not be accurate, it’s suggested that you consult with
your physician for accurate assessment.
There are 2 conditions under which the signal of IHB will be displayed:
1) The coefcient of variation (CV) of pulse period >25%.
2) The difference of adjacent pulse period≥0.14s, and the number of such
pulse takes more than 53 percentage of the total number of pulse.
13. Please do not use the cuff other than supplied by the manufacturer, otherwise it may bring biocompatible hazard and might result in measurement
error.
14. The monitor might not meet its performance specications or cause
safety hazard if stored or used outside the specied temperature and
humidity ranges in specications.
15. Please do not share the cuff with other infective person to avoid
cross-infection.
16. 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.
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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
17. 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.
18. Measurements are not possible in patients with a high frequency of arrhythmias.
19. The device is not intended for use on neonates, children or pregnant women.
(Clinical testing has not been conducted on neonates, children or pregnant
women.)
will be displayed.
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Note:
1. Please refer to the cuff circumference range in “SPECIFICATIONS” to make
sure that the appropriate cuff is used.
2. Measuring on same wrist each time.
3. Do not move your arm, body, or the monitor during measurement.
4. Stay quiet, calm for 5 minutes before blood pressure measurement.
5. Please keep the cuff clean. Clean the cuff by wet soft cloth and mild detergent
if the cuff becomes dirty. Do not remove the cuff from the monitor. Clean the
cuff after the usage of every 200 times is recommended.
6. Do not place the cuff around your wrist if the wrist has any inammation, acute
diseases, infections skin wounds.
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5. Body posture during measurement
Sitting Comfortably Measurement
a. Be seated with your feet at on the oor, and don’t cross
your legs.
b. Place palm upside in front of you on a at surface such
as a desk or table.
c. The middle of the cuff should be at the level of the right
atrium of the heart.
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6. Taking your blood pressure reading
a. After applying the cuff and your body is in a comfortable position, press the
“START” button. A beep is heard and all display characters are shown for selftest. See picture 6. Please contact the service center if segment is missing.
Picture 6 Picture 6-1 Picture 6-2 Picture 6-3
b. Then the monitor starts to seek zero pressure. See picture 6-1.
c. The monitor inates the cuff until sufcient pressure has built up for a meas-
urement. Then the monitor slowly releases air from the cuff and carries out the
measurement. Finally the blood pressure and pulse rate will be calculated and
displayed on the LCD screen separately. Irregular heartbeat symbol (if any)
will blink. See picture 6-2&6-3. The result will be automatically stored in the
memory bank.
d. After measurement, the monitor will turn off automatically after 1 minute of
PRODUCT DESCRIPTION
Based on Oscillometric methodology and silicon integrated pressure sensor,
blood pressure and pulse rate can be measured automatically and non-invasively. The LCD display will show blood pressure and pulse rate. The most recent 60 measurements can be stored in the memory with date and time stamp.
The Electronic Sphygmomanometers corresponds to the below standards:
IEC 60601-1Edition 3.1 2012-08/EN 60601-1:2006/A1:2013 (Medical electrical
equipment -- Part 1: General requirements for basic safety and essential performance), IEC60601-1-2:2014/EN 60601-1-2:2015 (Medical electrical equipment
-- Part 1-2: General requirements for basic safety and essential performance
- Collateral standard: Electromagnetic compatibility - Requirements and tests),
IEC80601-2-30:2009+AMD1:2013/EN 80601-2-30:2010/A1:2015 (Medical electrical equipment –Part 2-30: Particular requirements for the basic safety and
essential performance of automated non-invasive sphygmomanometers) EN
1060-1: 1995 + A2: 2009 (Non-invasive sphygmomanometers - Part 1: General
requirements), EN 1060-3: 1997 + A2: 2009 (Non-invasive sphygmomanometers - Part 3: Supplementary requirements for electro-mechanical blood pressure
measuring systems);ISO81060-2 : 2013(Non-Invasive Sphygmomanometers Part 2: Clinical Validation Of Automated Measurement Type).
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20. Motion, trembling, shivering may affect the measurement reading.
21. The device would not apply to the patients with poor peripheral circulation,
noticeably low blood pressure, or low body temperature (there will be low
blood ow to the measurement position).
22. The device would not apply to the patients who use an articial heart and
lung (there will be no pulse)
23. Consult your physician before using the device for any of the following conditions: common arrhythmias such as atrial or ventricular premature beats or
atrial brillation, arterial sclerosis, poor perfusion, diabetes, pre-eclampsia,
renal diseases.
24. The patient is an intended operator.
25. Attention that changes or modication not expressly approved by the party
responsible for compliance could void the user’s authority to operate the
equipment.
26. Swallowing batteries and/or battery uid can be extremely dangerous. Keep
the batteries and the unit out of the reach of children and disabled persons.
27. If you are allergic to plastic/rubber, please don’t use this device.
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no operation. Alternatively, you can press the “START” button to turn off the
monitor manually.
e. During measurement, you can press the “START” button to turn off the moni-
tor manually.
Note: Please consult a health care professional for interpretation of pressure measurements.
7. Displaying stored results
a. After measurement, you can review the results in the memory bank by press-
ing the “MEM” button. Alternatively, you can press “MEM” button in Clock
Mode to display the stored results. If it no result stored, LCD will show dashes
as picture 7, while press the button “MEM” or “START”, machine will turn off.
If there are results in the
memory bank, the LCD will
display the amount of the
results in the memory bank.
See picture 7-1.
Picture 7 Picture 7-1 Picture 7-2
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Picture 7-3 Picture 7-4 Picture 7-5
b. And then, the most recent result will be displayed with date and time stamp.
See picture7-2. Followed by, the blood pressure and pulse rate will be shown
separately. Irregular heartbeat symbol (if any) will blink. See picture7-3&7-4.
Press “MEM” button again to review the next result. See picture7-5. In this
way, repeatedly pressing the MEM button displays the respective results
measured previously.
c. When displaying the stored results, the monitor will turn off automatically after
1 minute of no operation. You can also press the button “START” to turn off
the monitor manually.
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MAINTENANCE
1. Do not drop this monitor or subject it to strong impact.
2. Avoid high temperature and solarization. Do not immerse the monitor
in water as this will result in damage to the monitor.
3. If this monitor is stored near freezing, allow it to acclimate to room
temperature before use.
4. Do not attempt to disassemble this monitor.
5. If you do not use the monitor for a long time, please remove the batteries.
6. It is recommended the performance should be checked every 2 years or after
repair. Please contact the service center.
7. Clean the monitor with a dry, soft cloth or a soft cloth squeezed well after
moistened with water, diluted disinfectant alcohol, or diluted detergent.
8. No component can be maintained by user in the monitor. The circuit
diagrams, component part lists, descriptions, calibration instructions, or other
information which will assist the user’s appropriately qualied technical
personnel to repair those parts of equipment which are designated repairably
can be supplied.
9. The monitor can maintain the safety and performance characteristics for a
minimum of 10,000 measurements or three years, and the cuff integrity is
maintained after 1,000 open–close cycles of the closure.
10. It is recommended the cuff should be disinfected 2 times every week if needed (For example, in hospital or in clinique). Wipe the inner side (the side con-
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Table 3
Proximity elds from RF wireless communications equipment
Test frequency
(MHz)
Band (MHz) Immunity test levels
Professional healthcare facility
environment
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385 380-390 Pulse modulation 18Hz, 27V/m
450 430-470 FM, ±5kHz deviation, 1kHz sine,
28V/m
710 704-787 Pulse modulation 217Hz, 9V/m
745
780
810 800-960 Pulse modulation 18Hz, 28V/m
870
930
8. Deleting measurements from the memory
When any result is displaying, keeping on pressing button “MEM” for three seconds, all results in the current memory bank will be deleted after three “beep”.
LCD will show picture 8, Press the button “MEM” or “START”, the monitor will
turn off.
Picture 8
9. Assessing high blood pressure for adults
The following guidelines for assessing high blood pressure (without regard
to age or gender) have been established by the World Health Organization
(WHO). Please note that other factors (e.g. diabetes, obesity, smoking, etc.) need
to be taken into consideration. Consult with your physician for accurate assessment, and never change your treatment by yourself.
Classication of blood pressure for adults
Sistolic
(mmHg)
SBP
BLOOD PRESSURE
Severe Hypertension
160
Moderate Hypertension
150
Mild Hypertension
140
High-normal BP
130
Normal BP
120
80 85 90 100 110
10. TECHNICAL ALARM DESCRIPTION
The monitor will show ‘HI’ or ‘Lo’ as technical alarm on LCD with no delay if
the determined blood pressure (systolic or diastolic) is outside the rated range
specied in part SPECIFICATIONS. In this case, you should consult a physician
or check if your operation violated the instructions.
The technical alarm condition (outside the rated range) is present in the factory
Diastolic
(mmHg)
CLASSIFICATION
Optimal
Normal
High-Normal
Grade 1 Hypertension
Grade 2 Hypertension
Grade 3 Hypertension
WHO/ISH Denitions and classication of blood pressure levels
120-129
130-139
140-159
160-179
mmHg
<120
≥180
DBP
mmHg
<80
80-84
85-89
90-99
100-109
≥110
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tacts skin) of the cuff by a soft cloth squeezed after moistened with Ethyl
alcohol (75-90%), then dry the cuff by airing.
11. The monitor requires 6 hours to warm from the minimum storage temperature
between uses until the monitor is ready for its INTENDED USE when the
ambient temperature is 20 °C.
12. The monitor requires 6 hours to cool from the maximum storage temperature
between uses until the monitor is ready for its INTENDED USE when the
ambient temperature is 20 °C
13. Not servicing/maintenance while the monitor is in use.
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1720 1700-1990 Pulse modulation 217Hz, 28V/m
1845
1970
2450 2400-2570 Pulse modulation 217Hz, 28V/m
5240 5100-5800 Pulse modulation 217Hz, 9V/m
5500
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EXPLANATION OF SYMBOLS ON UNIT
Follow instructions for use
Caution: read instructions (warnings) carefully
Type BF applied part
WEEE disposal
Medical Device complies with Directive 93/42/EEC
Manufacturer
Date of manufacture
Authorized representative in the European community
5785
Disposal: The product must not be disposed of along with other domestic waste. The users must dispose of this equipment by bringing it to a
specic recycling point for electric and electronic equipment. For further
information on recycling points contact the local authorities, the local
recycling center or the shop where the product was purchased. If the
equipment is not disposed of correctly, nes or penalties may be applied
in accordance with the national legislation and regulations.
GIMA WARRANTY CONDITIONS
Congratulations for purchasing a GIMA product. This product meets high qualitative standards both as regards the material and the production.
The warranty is valid for 12 months from the date of supply of GIMA.
During the period of validity of the warranty, GIMA will repair and/or replace free
of charge all the defected parts due to production reasons.
Labor costs and personnel traveling expenses and packaging not included.
All components subject to wear are not included in the warranty.
The repair or replacement performed during the warranty period shall not extend
the warranty. The warranty is void in the following cases: repairs performed by
unauthorized personnel or with non-original spare parts, defects caused by negligence or incorrect use. GIMA cannot be held responsible for malfunctioning on
electronic devices or software due to outside agents such as: voltage changes,
electro-magnetic elds, radio interferences, etc.
The warranty is void if the above regulations are not observed and if the serial
code (if available) has been removed, cancelled or changed.
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and cannot be adjusted or inactivated. This alarm condition is assigned as low
priority according to IEC 60601-1-8.
The technical alarm is non-latching and need no reset. The signal displayed on
LCD will disappear automatically after about 8 seconds.
11. Troubleshooting (1)
PROBLEM POSSIBLE CAUSE SOLUTION
LCD Display shows
abnormal result
The cuff position was
not correct or it was not
properly tightened
Body posture was not
correct during testing
Speaking, arm or body
movement, angry, excited
or nervous during testing
Irregular heartbeat
(arrhythmia)
Apply the cuff correctly
and try again
Review the “BODY POSTURE
DURING MEASUREMENT”
sections of the instructions
and re-test
Re-test when calm and
without speaking or moving
during the test
It is inappropriate for people
with serious arrhythmia
to use this Electronic
Sphygmomanometer
12. Troubleshooting (2)
PROBLEM POSSIBLE CAUSE SOLUTION
LCD shows low
battery symbol
LCD shows “Er 0” Pressure system is unsta-
LCD shows “Er 1” Fail to detect systolic
LCD shows “Er 2” Fail to detect diastolic
LCD shows “Er 3” Pneumatic system
LCD shows “Er 4 Pneumatic system leak-
Low Battery Change the batteries
ble before measurement
pressure
pressure
blocked or cuff is too tight
during ination
age or cuff is too loose
during ination
Don’t move and try again.
Apply the cuff correctly
and try again
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Serial number
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The defected products must be returned only to the dealer the product was purchased from. Products sent to GIMA will be rejected.
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IP22 Covering Protection rate
Keep in a cool, dry place
Keep away from sunlight
Product code
Lot number
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ELECTROMAGNETIC COMPATIBILITY INFORMATION
Table 1
Emission
Phenomenon Compliance Electromagnetic
RF emissions CISPR 11 Group 1,
Harmonic distortion IEC 61000-3-2
Voltage uctuations
and icker
Class B
Class A
IEC 61000-3-3
Compliance
environment
Home healthcare
environment
Home healthcare
environment
Home healthcare
environment
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PROBLEM POSSIBLE CAUSE SOLUTION
LCD shows “Er 5” Cuff pressure above
LCD shows “Er 6” More than 3 minutes
LCD shows “Er 7” EEPROM accessing error
LCD shows “Er 8” Device parameter
LCD shows “Er A” Pressure sensor
No response when
you press button
or load battery
300 mmHg
with cuff pressure above
15 mmHg
checking error
parameter error
Incorrect operation
or strong electromagnetic
interference
Measure again after ve
minutes. If the monitor is still
abnormal, please contact the
local distributor or the factory
Take out batteries for ve
minutes, and then reinstall
all batteries
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30
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Table 2
Enclosure Port
Phenomenon Basic EMC
standard
Electrostatic Discharge IEC 61000-4-2 ±8 kV contact
Radiated RF EM eld IEC 61000-4-3 10V/m
Proximity elds from RF
wireless communications
equipment
Rated power frequency
magnetic elds
IEC 61000-4-3 Refer to table 3
IEC 61000-4-8 30A/m
Immunity test levels
Home Healthcare
Environment
±2kV, ±4kV, ±8kV, ±15kV
air
80MHz-2.7GHz
80% AM at 1kHz
50Hz or 60Hz
32918 / KD-735
ANDON HEALTH CO., LTD.
No. 3 JinPing Street, Ya An Road,
Nankai District,
Tianjin 300190, China
Made in China
Imported and distributed by:
Gima S.p.A. - Via Marconi, 1
20060 - Gessate (MI) Italy
iHealthLabs Europe SAS
36 Rue de Ponthieu,
M32918-GB-Rev.2-10.19
75008, Paris, France
IP22
0197
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