Arm Blood Pressure Monitor Instruction Manual Model: AES-U393 Version:1.
Table of Contents 1. Introduction ..................................................................................................................................... 3 2. Indications for Use ........................................................................................................................... 3 3. Product information ........................................................................................................................ 3 4. Classification ......................
1. Introduction Thank you for purchasing the Arm Blood Pressure Monitor. The blood pressure monitor uses the oscillometric method of blood pressure measurement. This means the monitor detects your blood’s movement through your brachial artery and converts the movements into a digital reading. An oscillometric monitor does not need a stethoscope so the monitor is simple to use.
. Classification (1) Internally powered equipment; (2) Type BF applied part; (3) IP classification: IP21; (4) Disinfection of 70% medical alcohol; (5) Not Category AP / APG equipment; (6) Mode of operation: continuous operation. 5. Safety Information 5.1 General usage Do not adjust medication based on measurement values from this blood pressure monitor. Take medication as prescribed by your physician.
The user must check that the equipment functions safely and see that it is in proper working condition before being used. If this equipment is modified, appropriate inspection and testing must be conducted to ensure continued safe use of the equipment. The patient can use and maintain the device as an operator. Please do not continue to use the cuff if you are allergic to it.
Indicates temperature limits within which the transport package shall be stored and handled. Lot number Product number The device should not be used after the end of the shown or the day Manufacturer Authorized Representative in the European Community CE mark: indicates that the device complies with the EU 2017/745 IP21 Protected against solid foreign objects of 12.5mm Protection against vertically falling water drops. Medical Device Non-ionizing electromagnetic radiation. 7.
8. Display 9. Battery Installation 1. Remove the battery cover by pushing it in the direction of the arrow. 2. Install 4×AAA batteries and make sure the poles are in the right direction. 3. Replace the battery cover. Note: When the symbol of low battery “ ” is flashing, please replace new batteries immediately. After that, the date and time need to be reset. If the blood pressure monitor will not be used for a long time, please remove the batteries. Do not mix different type of batteries.
To ensure the battery performance, please stored the device (battery) in the dry and cool indoor environment. Please stop using when you find the battery was bulging or leaks, replace new batteries immediately. 10. Setting the User, Voice and Unit Turn off the unit. Step1: press and hold the SET button for about 3 seconds, when the User ID symbol which is on the top of the screen is flashing, means enter the user setting mode.
the same level as your heart. Please sit down and be quiet, do not talk and move your body during the measurement. Patients with arrhythmia and atherosclerosis should not measure by themselves if there is no medical staff there. Avoid any electromagnetic interference or noise interference during measurement. Keep a record of your blood pressure and pulse readings for your physician. A single measurement does not provide an accurate indication of your true blood pressure.
13. Correct Measurement Posture 1. Correct posture: sit on a chair as shown in the figure below with your feet flat on the floor. Place your arm on the table so the cuff is level with your heart. Relax yourself for the measurement. 2. Keep quiet during the measurement. Do not shake, talk or eat to avoid inaccuracy. 3. Since blood pressure can vary from time to time throughout the day, please take measurements at the same time every day to ensure reliability. 14. Taking A Measurement 1.
15. Viewing Memory Values The monitor automatically stores up to 90 sets of measurement values for each user. Turn off the unit. Step1: press the MEM button, average of the last three sets of measurement values displays first on the screen. Step2: press the MEM button to view each measurement value. 16. Deleting Memory Values In shutdown mode, press and hold the MEM button, after about 3 seconds press the SET button at the same time, “ ” appears on the display, means all the memories have been deleted.
Use a soft moistened cloth and soap to clean the arm cuff, do not wash it in water. Never immerse the monitor or any of the components in water. 18.2 Maintaining the monitor and cuff Keep the monitor and cuff in the storage box when not in use. Do not forcefully bend the arm cuff or air tube. Do not fold tightly. Do not press the START/STOP button before wear the cuff properly. Do not disassemble or attempt to refit the unit or components.
Measurement range Measurement accuracy Memories recall Dimensions Weight Power supply Type-C power supply Switch off Included in delivery Cuff size is suitable for arm size Product life Battery life Adapter Diastolic: 30-200mmHg Systolic: 60-255mmHg Pules: 40-199 pulses/min Pressure: ±3mmHg (±0.4kPa) Pules: ±5% of reading 90 measurement recalls each user 150mm×85mm×41mm About 182g (without batteries) DC 6.
23.Disposal This marking shown on the product or its literature, indicates that it should not be disposed with other household wastes at the end of its working life. To prevent possible harm to the environment or human health from uncontrolled waste disposal, please separate this from other types of wastes and recycle it responsibly to promote the sustainable reuse of material resources.
Table 1 Guidance and manufacturer’s declaration - electromagnetic emissions Emissions test Compliance RF emissions Group 1 CISPR 11 RF emissions Class B CISPR 11 Class A Harmonic emissions IEC 61000-3-2 Applied Voltage fluctuations/ flicker emissions IEC 61000-3-3 Table 2 Guidance and manufacturer’s declaration - electromagnetic Immunity Immunity Test IEC 60601-1-2 Compliance level Test level Electrostatic discharge (ESD) ±8 kV contact ±8 kV contact IEC 61000-4-2 ±2 kV, ±4 kV, ±8 kV, ±15 kV
Single phase: at 0 Single phase: at 0 0% 300 cycle 0% 300 cycle Power frequency magnetic field 30 A/m 30 A/m IEC 61000-4-8 50Hz/60Hz 50Hz/60Hz Conduced RF 150KHz to 80MHz： 150KHz to 80MHz： IEC61000-4-6 3Vrms 3Vrms 6Vrms (in ISM and amateur 6Vrms (in ISM and amateur radio bands) radio bands) 80% Am at 1kHz 80% Am at 1kHz Radiated RF 10 V/m 10 V/m IEC61000-4-3 80 MHz – 2,7 GHz 80 MHz – 2,7 GHz 80 % AM at 1 kHz 80 % AM at 1 kHz NOTE UT is the a.c.
iDEN 820, CDMA 850, LTE Band 5 1720 1 700 – GSM 1800; Pulse 1845 1 990 CDMA modulation 1900; 217 Hz 1970 2 0.3 28 2 0.3 28 0,2 0.3 9 GSM 1900; DECT; LTE Band 1, 3, 4, 25; UMTS 2450 2 400 – Bluetooth, Pulse 2 570 WLAN, modulation 802.11 217 Hz b/g/n, RFID 2450, LTE Band 7 5240 5 100 – WLAN Pulse 5500 5 800 802.11 modulation a/n 217 Hz 5785 25.FCC Warning This device complies with part 15 of the FCC Rules.
-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. FCC RF Radiation Exposure Statement: 1. This Transmitter must not be co-located or operating in conjunction with any other antenna or transmitter. 2. This equipment complies with RF radiation exposure limits set forth for an uncontrolled environment. The device has been evaluated to meet general RF exposure requirement.
