iBloodPressure LD-575 Upper Arm Automatic Cellular Blood Pressure Monitor Instruction Manual
- June 16, 2024
- iBloodPressure
Table of Contents
- PARTS AND CONPONENTS
- GENERAL
- IMPORTANT SAFETY INSTRUCTIONS
- BATTERY INSTALLATION
- USING AN AC ADAPTER
- UISING THE DEVICE
- CORRECT POSTURE
- APPLYING THE CUFF
- TAKING A MEASUREMENT
- IRREGULAR HEARTBEAT DETECTOR
- WHO CLASSIFICATION INDICATION
- ERROR AND LOW BATTERY INFORMATION
- TROUBLESHOOTING
- CARE, STORING, REPAIRAND RECYCLING
- SECIFICATIONS
- MANUFACTURER’S DECLARATION
- Use of this equipment adjacent to or stacked with other equipment should be
- QUALITY GUARANTEE
- REQUIRING RECORD
- PERIODIC SAFETY CHECKS
- Documents / Resources
UPPER ARM AUTOMATIC
CELLULAR BLOOD PRESSURE MONITOR
INSTRUCTION MANUAL
Model: LD-575
PARTS AND CONPONENTS
- Main Body
- LCD Display
- Air Connector
- Tube Plug
- Air Hose
- Cuff
- D-ring
- Batteries
SYMBOLS
Symbols | Meaning |
---|---|
Manufacturer | |
Authorized Representative i the European community | |
**** | The device, accessories and the packaging have to be disposed correctly |
at the end of the usage. Please follow Local Ordinances or Regulations for
disposal.
| Keep dry
| Attention, consult accompanying documents
| Type BF Applied Part
| Stand by
GENERAL
This instruction manual is intended to assist the user with safe and efficient
operation of the automatic digital blood pressure monitor (hereinafter:
device) model iBloodPressure. The device must be used in accordance with the
procedures described in this manual. It is important to read and understand
the entire manual, especially the section < IMPORTANT SAFETY INSTRUCTIONS >.
This device s intended for the non-invasive measurement of systolic and
diastolic arterial blood pressure and pulse rate in adults and children 15
years old and above.
CAUTION:
- Do not use this device on infants or persons who cannot express their intentions.
- The device is not suitable for measuring the blood pressure of children under 15 years of age.
- People who suffer from arrhythmia, cardiovascular problems or who have had a stroke should consult their doctor before using the device.
PRINCIPLE OF OPERATION
This device adopts the oscillometric technology with Fuzzy Algorithm to
measure the arterial blood pressure and pulse rate. The cuffis wrapped around
the arm and automatically inflated by the air pump. The sensor of the device
catches weak fluctuation of the pressure in the cuff produced by extension and
contraction of the artery of the arm in response to each heartbeat. The
amplitude of the pressure waves is measured, converted to millimeters of the
mercury, and is displayed by a digital value.
ATTENTION: This device can not provide reasonable accuracy if used or
stored in the temperature, humidity or altitude beyond the range stated in the
section
NEW TECHNOLOGIES USED
Fuzzy Algorithm is the processing algorithm, taking into account the specialty
of individual heartbeats, which provides higher accuracy of measurement.
Software version: V1.1
IMPORTANT SAFETY INSTRUCTIONS
It is necessary to know that arterial blood pressure is subjected to
fluctuations. The level of the arterial blood pressure depends on many
factors. Generally arterial blood pressure is lower in summer and higher in
winter. Arterial blood pressure changes with atmospheric pressure and is
affected considerably by many factors, medications, drinking, and smoking can
greatly affect the level of an individual’s blood pressure. Blood pressure
does vary with age
Please read the instruction manual carefully before using this device,
especially
- Consult your physician before use if you have an electrical implant.
- I you had a mastectomy do not use this blood pressure monitor on the arm on the side of the mastectomy.
- Pregnant women should only measure their own blood pressure in consultation with their doctor, since the readings may be affected by pregnancy.
- Do not service or maintain the cuff while in use.
- Do not use this blood pressure monitor on any arm where intravascular access or therapy (such as an intravenous drip or a blood transfusion), or an arteriovenous shunt (A-V shunt) is present. The temporary interference to blood flow by the blood pressure measurement could result n injury.
- Do not use the device with other medical electrical (ME) equipment simultaneously.
- Do not use the device in the area the HF surgical equipment, MRI, or CT scanner &xists, or in the oxygen rich envirorment.
- Do not use a mobile phone or other devices that emit electromagnetic fields, near the device. This may result in incorrect operation of the device.
- Never use any accessories or parts from other manufacturers. Using such accessories or parts could cause a hazardous situation for the user or damage to the device.
- Do not modify this equipment without authorization of the manufacturer.
- The batteries used in this device may present a fire or chemical bum hazard if mistreated. Do not disassemble, heat or incinerate.
- Keep equipment away from fire and heat sources to prevent fire or explosion
- Please keep the unit out of reach of infants, children under 15 or pets, since inhalation or swallowing of small parts can be dangerous or even fatal
- The continuous cuff pressure may cause harmful injury if the tubing has kinks.
- Do not use an extension cord with this device.
- Keep out of reach of children under 15.
- Do not put the air tube around your neck – this may result in suffocation!
- Adevice should never be left unattended when plugged in.
- Do not reach for a corded device that has fallen into water. Unplug immediately.
- It is quite normal that two measurements taken in quick succession may produce significantly different results, because too frequent and consecutive measurements could cause disturbances in blood circulation and injuries.
Cautions
- Use this device under the right environmental conditions s indicated in this user manual. If not, this could affect the performance, lifetime of the device and measurement results.
- Only use this device for its intended purpose as described in this user manual.
- Do not confuse self-monitoring with self-diagnosis. This device allows you to monitor your blood pressure. Do not begin or end medical treatment based on the measurement results. Always consult your physician for treatment advice.
- Do not take any therapeutic measures on the basis of a self-measurement.
- Never change prescribed medication without consulting your physician. Consult your physician if you have any questions about your blood pressure.
- If you are taking medication, consult your physician to determine the most appropriate time to measure your blood pressure.
- Consult the physician if measurement errors oceur in children or persons with arhythmia.
- The pulse display is not suitable for monitoring the frequency of cardiac pacemakers.
- Common arhythmias (such as atrial or ventricular premature beals or atrial fibrillation) and peripheral artery disease / arteriosclerosis can affect the accuracy of this blood pressure monitor. Please consult your physician on how to best use this blood pressure monitor if you suffer from any of these conditions. Blood pressure measurement is not suitable in cases of serious arteriosclerosis (hardening of the arteries)
- Always check the device and cuff before you use it. Do not use the device or cuff if one of them is damaged, because this may cause injury.
- This device is not intended for use on extremities other than the arm or for functions other than obtaining a blood pressure measurement.
- Do not attach the cuff on the same arm on which other monitoring medical electrical equipment is attached simultaneously, because this could cause temporary loss of function of those simultaneously-used monitoring medical electrical equipment
- Never attach the cuff on injured skin, an injured arm or an arm under medical treatment as this can cause further injury.
- Do not forcibly crease the arm cuff or the air tube excessively.
- Do not press the air tube while taking a measurement.
- Do not use the device in the case of existing polyester or nylon material allergies.
- This device is not suiitable for continuous monitoring during medical emergencies or operations.
- This device cannot be used with HF (High Frequency) surgical equipment at the same time.
- This device is not washable. Never immerse the device in water and do not rinse it under the tap.
- This device should be kept dry to prevent moisture buildup.
- The equipment is not AP/APG equipment and is ot suitable for use in the presence of a flammable anesthetic mixture with air, with oxygen or nitrous.
- To avoid measurement errors, do not use the device near strong electromagnetic fields, radiated interference signal or electrical fast transientiburst signal. For example magnets, radio transmitters, microwave ovens.
- If this device was stored in cold temperatures, let it sit at room temperature for at least 1 hour.
- Repeated measurements with an interval of 3 minutes are recommended, o you can calculate the average to get a more accurate measurement. An interval of 3 minutes can also ensure that the operation of the device does not result in prolonged impairment of the circulation of the blood.
- Atherosclerosis patients may require longer intervals (10-15minutes) as elasticity of patients blood vessels decreases significantly with the disease.10-15 minute intervals are also recommended for patients who have been living with diabetes for along period of time.
- Dispose of the device, components and optional accessories according to applicable local regulations. Unlawful disposal may cause environmental pollution.
CLASSIFICATION
- ME EQUIPMENT not intended for use in an oxygen rich environment or in the presence of flammable mixers.
- Intemally powered equipment (without adapter), Class II equipment (with adapter).
- Type BF applied part, recognize the cuff as applied part.
BATTERY INSTALLATION
- 0pen the battery cover and install four “AA’ type batteries into the battery compartment as indicated. Make sure that the polarity is correct;
- Close the battery compartment cover.
- Replace the batteries when the replacement indication “appears in the gisplay or nothing happens after the &” button is pressed;
- Use AA alkaline batteries, do not use rechargeable batteries;
- Only the same type of batteries should be used together;
- Replace all batteries simultaneously;
- If the device is to be unused for a long time, please take out the batteries;
- Don’tleave the worn batteries in the device.
USING AN AC ADAPTER
Besides batteries you can use an AC adapter as the power supply. The AC
adapter is optional for this device and is sold separately.
The AC adapter is specified as a part of the blood pressure monitor.
Insert the AC adapter cord into the jack on the right side of the monitor
- Insert the AC adapter plug into the outiet,
- To remove the AC adapter, disconnect the adapter plug from the AC outlet first and then disconnect the cord from the monitor’s jack.
Caution
- When using optional AC adapter, the AC adapter must comply with the requirements of standard IEC60601-1
- To avoid possible damage of the monitor, use only the exclusive AC adapter that can be purchased from authorized dealers. Other adapters may damage the blood pressure monitor.
- The AC adapter is used as an isolating means, the AC adapter plug shall insert into the outlet nearby the operator, making it easy to disconnect the device from the outlet
- If you have been using the device for a long time, let the adapter cool before moving the plug to prevent burn
- Plug the AC adapter into the appropriate voitage outiet. Do not use in a multi-outiet plug.
- Do not position the blood pressure monitor so that is difficult to disconnect the adapter.
Note: The monitor is designed not to draw power from the batteries when the
AC adapter is in use.
Optional AC adapter technical features:
Model:YS5M-0600600
Input:100-240V 50/60Hz
Output voltage: 6V:5%
Output current: 600 mA
UISING THE DEVICE
The iBloodPressure digital blood pressure monitors have builtin SIM cards that can transmit data to your care team.
-
After the device is powered on, it will enter the automatic time update function first as shown in Fig 1
-
After the time is updated, the standby screen is displayed as shown in Fig 2
-
If you don’t want to update the time, press the button to exit and enter standby mode or turn off the device.
Caution:
- Please keep quiet for 5-10 minutes and avoid eating, drinking, alcohol, smoking, exercising and bathing before taking a measurement. All these factors may influence the measurement result.
- Remove any garment that fits closely to your upper arm
- Always measure on the same arm (normally left).
- Measurements should be taken regularly at the same time of each day, as blood pressure varies throughout the day.
- Any effort to support the arm during measurement may increase the measured blood pressure.
- Make sure you are in a comfortable, relaxed position with uncrossed legs, feet. – flat on the floor, back and arm supported, middle of the cuff at the level of the right atrium of the heart and do not move or constrict your muscles or talk during measurement.
- Use a cushion to support your arm if necessary. Maintain this position for the entire measurement.
- If the arm artery lies lower or higher than the heart, a false reading may be obtained
- Aloose or open cuff may cause false readings.
- With repeated measurements, blood accumulates in the arm which can lead to false readings.
- Consecutive blood pressure measurements should be repeated after a 3 minute pause or after the arm has been held up in order to allow the accumulated blood to flow away.
CORRECT POSTURE
-
Sit at a table and let the table support your arm as you take the measurement.
-
Sit upright with your back straight
-
Make sure that the cuff on the upper arm and is at approximately the same level as the heart.
-
Make sure your feet are flat on the ground and are not crossed
-
You may lie on your back and take a measurement Look at the celling, keep calm, and don’t move your neck or body during the measurement
APPLYING THE CUFF
-
Insert the edge of the cuff approximately 5 centimeters into the D-ring as shown.
-
Put the cuff on the left upper arm with the tube pointing to the direction of palm. If measuring on your left am s difficult, you can use your right am for measurement. In this case, it is necessary to know that the readings may differ about 5-10 mmHg between your left arm and right arm.
-
Wrap the cuff around your upper arm with the lower edge of the cuff approximately 1 inch above the elbow. The mark
must be over the artery of the am. -
Press the ouff to make sure that it is attached securely. The cuff should not be too tight or loose. The cuff should be tight while still being able to easily it two fingers between the cuff and your am.
-
The mark
on the cuff must point to area . This means the cuff size is correct. If mark points o the area beyond area , please consult your care team on whether you need another size cuff. This device is supplied with the standard cuff range between 8.66-12.60 inch. -
Sometimes it is difficult to make the cuff lay flat depending on the shape of the user’s upper arm, the cone-shape assembly of cuf s also acceptable.
-
If your clothes restrict the blood circulation of your upper arm, or you roll your sleeve p 50 as to result in such restriction, please take off your shirt to get an accurate measurement if necessary.
Caution:
If you experience discomfort during a measurement, such as pain in the upper
arm or other complaints, press the * & button to release the air immediately
from the cuff. Loosen the cuff and remove it from your arm.
TAKING A MEASUREMENT
-
Insert the tube plug into the air connector. Before the measurement, take 3-5 deep breaths and relax your body. Don’t talk or move your arm;
-
Press the ‘( ****) bution, and all symbols will appear on the Fa=gz g display in 2 seconds as shown in Fig 2. The cuff will begin p to inflate with the display showing the reading of the pressure as show in Fig 3;
-
The pressure in the cuff will increase to working pressure. Then the pump stops and pressure falls quickly.during which the user’s blood pressure and pulse will be calculated as shown in Fig 4;
-
After the measurement, the systolic pressure, diastolic pressure, and pulse rate wil show in the display as shown in Fig 5. At the same time, the * Sending” icon is displayed, indicating that data is being uploaded;
-
The time of measurement will also be displayed. The time is automatically synchronized during data upload.
-
When the Sending Done ” icon is displayed as shown in Fig 6, the data transmission is successful. When the Sending Failed icon is displayed as shown in Fig 7, the data transmission has failed.
-
If you don’t want to transmit data, press the bution * ( ***) to tum off the device. Please rest for at least 3 minutes for another measurement. If the power supply is not switched off and the device remains unused for 3 minutes, the device will be switched off automatically.
Caution:
‘The measurement results are saved only when the transmission fails or the
data is forced to be transmitted. After the measurement data is transmitted,
the machine will automatically detect the stored memory data. If there is any
memory data that has not been transmitted, it will send the data that has not
been transmitted first.
RAPID DEFLATION DURING MEASUREMENT
If you do ot feel well during measurement or want to stop the measurement for
some reason, you can press the “( ****)” button. The device will quickly
release the air in cuff and the device will be returned to standby mode.
IRREGULAR HEARTBEAT DETECTOR
The iBloodPressure digital blood pressure monitor provides a blood pressure
and pulse rate measurement even when an imegular heartbeat occurs. When the
device detects the irregular heartbeat or any excessive body movement during
measurement, the icon will display in the LCD as shown in Fig 8. It is
important that you are relaxed, remain still and do not talk during
measurement.
Notice: We recommend contacting your physician if you see this indicator
frequently.
WHO CLASSIFICATION INDICATION
Standards for assessment of high or low blood pressure, regardiess of age,
have been established by World Health Organization (WHO) as show in the chart
as below: The chart displays classifications, based on current data,
corresponding to the WHO classifications.
For example, if your blood pressure is 145mmHg (systolic pressure), 88mmHg
(diastolic pressure), according to the World Health Organization standard,
your blood pressure level is Mild Hypertension.
Note: If the systolic blood pressure and the diastolic blood pressure
fall into different categories, the higher value should be taken for
classification.
ERROR AND LOW BATTERY INFORMATION
INDICATION | POSSIBLE REASON | CORRECTION METHODS |
---|---|---|
The cuff is put on incorrectly or the tube plug is inserted too loosely. |
Movement of arm/hand talking during measurement.
The cuff is not inflated to
necessary pressure.| Make sure that cuff is put on correctly and the tube plug
is inserted tightly and repeat the measurement.
Repeat the measurement while closely following the recommendations outlined in
this manual.
| The batteries are weak| Replace all 4 batteries with new ones.
TROUBLESHOOTING
SYMPTOM | CHECK POINT | REMEDY |
---|---|---|
No display when the device is powered on. | The batteries have run down. The |
polarity of the batteries is wrong. The contact of the battery compartment is
polluted.| Replace all the batteries with new ones.
Install the batteries correctly. Clean the battery terminals with dry cloth.
Inflation stops and reinflates later.| The automatic inflation feature for
ensuring correct measurement. Did you talk or move your arm (or hand) during
measurement?| Keep quiet and silent during the measurement.
The reading is extremely low or high.| Is the cuff at the same level as the
heart?
Is the cuff wrapped correctly? Did you strain your arm during measurement?
Did you talk or move your arm
(or hand) during measurement?| Make sure that your posture is right.
Wrap the cuff correctly.
Relax during measurement. Keep quiet and silent during the measurement.
Pulse rate is too low or too high.| Did you talk or move your arm (or hand)
during measurement? Did you make measurement right after exercise?| Keep quiet
and silent
during the measurement. Take measurement again after resting for more than 5
minutes.
The batteries run out quickly.| Faulty batteries are used.| Use alkaline
batteries of known manufacturers.
CARE, STORING, REPAIRAND RECYCLING
-
It’s necessary to protect this device against high moisture, direct sunlight, shock, solvent, alcohol and gasoline.
-
Remove the batteries if the device is being stored for a long time, and keep the batteries far away from children.
-
Keep the cuff away from sharp objects and don’t extend or twist the cuff
-
This device is not washable. Never immerse the device in water and do not finse it under the tap.
-
Do not clean or perform maintenance on the device when itis in use with a patient.
-
The cuff is sensitive and must be handled with care. You can clean the cuff with a damp cloth for daily maintenance. To avoid cross infection when sharing the cuff, you can sterilize the fabric cover of the cuff with cotton balls moistened by 3% solution of hydrogen dioxide. After prolonged use there will be a partial discoloration on the fabric of the cuff. Do not launder or iron the cuff as well as ironing with a hot flatiron.
WARNING: Under no circumstances may you wash the inner bladder! -
Since neither the device nor batteries are household waste, follow your local recycling rules and dispose of them at an appropriate collection site.
-
Do not open the device, or delicate electrical components such s an intricate air unit could be damaged. If you can not fix the problem using the troubleshooting instructions, please request service from your dealer.
WARNING: Do not repair the device without manufacturer’s authorization.
Do not carry out maintenance when using the device.
Caution:
Generally, we recommend the device should be inspected every 2 years and
utilize the manometer mode to verify the accuracy of the manometer at least at
50mmHg and 200mmHg after maintenance and repair. Please contact your dealer
for maintenance.
SECIFICATIONS
Model | iBloodPressure (LD-575) |
---|---|
-Size | 13404-x98(W) k57(N)mm |
Weight | Approximately 236g without batteries |
Measuring method | Oscillometry |
Measuring range | 40 to 180mmHg(DIA.dlastolic pressure) 60 to |
260mrnHg(SYS,systolic pressure) 40 to 160 bears/minute (PUL,pulse
Measuring accuracy| t 3 mmHg for static pressure
t 5% of the reading for the pulse rate
Inflation| Automatic by the pump
Rapid deflation| Automatic electronic valve
Batteries| Optional component. 4″AA’t 1.5V
Adapter| Optional component, 6V, 600mA
Operation temperature and humidity, air pressure| +10 C to + 40 C , 85% and
below 800hPa to 1060hPa
Transport and storage temperature and humidity, air pressure| -20 C to + 50 C
• 85% and below 500hPa to 1060hPa
Upper arm circumference| Applicable for arm circumference 8.66-12.60 inch.
(standard cuff)
Complete kit| Main body, cuff, 4 kAA batteries
(optional), adapter (optional), gift box, instruction manual
Overvoltage category| Category II
HONSUN (NANTONG) Co,, Ltd.
Address:No.8 Tongxing Road Economic & Technological Development
Area 226009 Nantong City PEOPLE’S REPUBLIC OF CHINA
SHANGHAI INTERNATIONAL HOLDING CORP. GMBH (EUROPE)
Address: Eiffestrasse 80, 20537 Hamburg GERMANY
MANUFACTURER’S DECLARATION
Compliance information for each EMC test
Electromagnetic Emission(Home Healthcare Environment)
Emission test(IEC60601-1 -2:2014)| Compliance
Conducted and radiated RF emissions| CLSPR 11 Group 1 Class B
Harmonic emissions IEC 61000-3-2| Class A
Voltage fluctuationsiflicicer emissions IEC 61000-3-3| Complies
Compliance information for each EMC test
Declaration-Electromagnetic Immunity(Home Healthcare Environment)
Immunity test| IEC 60601 test level| Compliance level
Conducted RF IEC 61000.44| 3V
150 kHz to 80 MHz
6V in ISM and amateur radio bands between 0.15MHz and 80MHz| 3V
150 kl-lz to 80 MHz
6V in ISM and amateur radio bands between 0.15MHz and 80MHz
Radiated RF IEC 61000-4-3| 10 V/m
80 MHz to 2.7 GHz
also meet the requirement of table 9 of 60601-1-2:2014| 10 V/m
80 MHz to 2.7 GHz
also meet the requirement of table 9 of 60601-1-2:2014
Electrostatic discharge (ESD)
IEC 61000-4-2| 38 kV contact
*2 kV,±4 kV,38 kV,315 kV air| 38 kV contact
32 0434 kV,±8 kV,315 IN air
Electrical fast transient/burst IEC 61000-4-4| ±2 kV for power supply lines|
±2 kV for power supply lines
Surge IEC 61000-4-5| 30.5 kV,2 1 IN line(s) to lines| 30.5 liV,t 1 kV line(s)
to lines
Compliance information for each EMC test
Declaration-Electromagnetic | Immunity(Horre | Healthcare Environment) |
---|---|---|
Immunity test | IEC 60601 test level | Compliance level |
Voltage dips, short
interruptions and voltage
variations on
power supply
input lines IEC
61000-4-11| 0% UT, 0.5 Cycle at 00.450.90°.
135°,180°. 225°, 270°, 315° 0% UT.1 Cycle and 70% UT. 2.5✓30 cycles
stole phase:at 0°
0% UT,250/300 cycles| 0% UT. 0.5 Cycle at 0°.45°.90°,
135°,180°, 225°, 270°, 315° 0% UT, 1 Cycle and 70% Ur, 25 cycles
sigle phase:at 0°
0% UT,250cycles
Power frequency (50/60Hz) magnetic field IEC 610004-8| 30 Arm| 30 A/m
NOTE: The EUT is the a.c. mains voltage prior to application of the test
level.
“The following phenomenon is stil fulfl the requirement of basic safety and
essential performance.
UT:230V ~/50Hz The pressure of the EUT is eviation the normal value but the value is stil more than 10psi when flow is 4.5limin.
+UT:230V ~/50Hz The EUT stop working when adding 0%UT but the EUT can restore its normal mode automatically.
Use of this equipment adjacent to or stacked with other equipment should be
‘avioded because it could result in improper operation. If such use is
necessary, this equipment and the other equipment should be observed to verify
that they are operating normally.
Portable RF communications equipment(including peripherals such as antenna
cables and external antennas) should be used no closer than 30cm(12 inches to
any part of this devie, inluding cables specificed by the manufacturer.
Otherwise, degradation of the performance of this equipment could result *
Under the test condition specified in immunity, the product can provide the
basic safety and essential performance.
Ifthe essential performanceis-lostor degraded,additional measures are
necessary,such as reorienting or relocating the device.
QUALITY GUARANTEE
MODEL|
---|---
Warranty period| Two years from purchasing date
Purchasing date|
Purchasing shop| Name:| Telephone:
Address:
Customer| Name:| Telephone:
Address:
- Warranty for this automatic digital blood pressure monitor is 24 months from the date of purchase. The 24 months warranty excludes the monitor cuff.
- The warranty obligations are prescribed for by warranty certficate for buyer.
- The addresses of organizations for guaranteed maintenance are present in the warranty certficate.
WARNING
Do not modify this equipment without authorization of the manufacturer. All
major maintenance on the device must be performed by an authorized service
center or distributor. No use-serviceable parts inside, before servicing to
authorized representative or manufacturer.
DECLARATION:
When technical information for user or service personnel requirements is not
in the scope of confidentiality of the Company, the Company committed to
provide information disclosure in accordance with procedure, including circuit
diagrams and parts lists, and other related type technology information that
do not involve commercial secrets may be disclosed. Access to information
channels and procedures, please contact your dealer or manufacturer.
REQUIRING RECORD
Date | TROUBLE | SERVICE MAN |
---|---|---|
Guarantee
Regulation| 1.During warranty period the repair could be made at any BPM
repair department.
2.The following things void the warranty:
(1)Operating BPM differently from procedures or Instructions of the manual.
(2)The body is damaged intentionally.
(3)Self-repairing or modifying the monitor construction in any way.
(4)Breakdown due to corrosion of battery leakage.
(5)Problem which occurs under natural calamity and other force majeu res.
PERIODIC SAFETY CHECKS
If you use the device with a power adapter, preventive inspection and maintenance should be performed including the frequency of such maintenance.
- Every time before use, please check the adapter. If damaged, do not use.
- Please clean the prongs of adapter plug at least once a year. Too much dust on plug may cause the fire.
The manufacturer reserves the right to make technical changes without notice
in the interest of progress.
Prior notices will not be given in case of any amendments within this manual.
The mentioned trademarks and names are owned by the corresponding ccompanies.
MADE IN CHINA
P575/2207/01
Documents / Resources
|
iBloodPressure LD-575 Upper Arm Automatic Cellular Blood Pressure
Monitor
[pdf] Instruction Manual
LD-575 Upper Arm Automatic Cellular Blood Pressure Monitor, LD-575, Upper Arm
Automatic Cellular Blood Pressure Monitor, Arm Automatic Cellular Blood
Pressure Monitor, Automatic Cellular Blood Pressure Monitor, Cellular Blood
Pressure Monitor, Blood Pressure Monitor, Pressure Monitor, Monitor
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