Omron HBP-1120 Instruction Manual
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Omron HBP-1120 Instruction Manual

Professional blood pressure monitor
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Professional Blood Pressure Monitor
• Instruction Manual
• Mode d'emploi
• Gebrauchsanweisung
• Manuale di istruzioni
• Manual de instrucciones
• Gebruiksaanwijzing
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Thank you for purchasing this OMRON Professional Blood Pressure Monitor.
Read this manual to ensure the safe and accurate use of the monitor.
HBP-1120
Issue Date/Date de publication/Ausgabedatum/
Data di pubblicazione/Fecha de publicación/
IM-HBP-1120-E-05-07/2022
2829457-8D
: 2022-08-30
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  • Page 1 • Manuale di istruzioni • Manual de instrucciones • Gebruiksaanwijzing • Thank you for purchasing this OMRON Professional Blood Pressure Monitor. Read this manual to ensure the safe and accurate use of the monitor. IM-HBP-1120-E-05-07/2022 2829457-8D Issue Date/Date de publication/Ausgabedatum/ Data di pubblicazione/Fecha de publicación/...

  • Page 2: Table Of Contents

    Table of Contents Introduction Intended Use ..................1 Exemptions ....................2 Notes on Safety ..................3 Using the Unit Components of the Product ..............9 Options ....................9 Features of the Product ............... 10 Features / Functions of Unit ..............11 Installing the Batteries ................ 13 Connecting the AC Adapter ..............

  • Page 3: Introduction Intended Use

    Introduction Intended Use Medical Purpose The device is a digital monitor intended for use in measuring blood pressure and pulse rate in adult and pediatric patient population with arm circumference ranging from 12 cm to 50 cm (from 5 inches to 20 inches). Intended User This device should be used by a medical professional.

  • Page 4: Exemptions

    OMRON will not bear any responsibilities on the following matters. 1. When a problem or damage occurs caused by the maintenance and/or repair conducted by a person other than OMRON or the dealer specified by OMRON 2. The problem or damage of OMRON product caused by the product of other manufacturer not delivered by OMRON 3.

  • Page 5: Notes On Safety

    • Do not use the cuff or AC adapter to lift the unit, it can also cause the unit to malfunction. • If the unit has broken down, contact your OMRON retail dealer or distributor. • Do not use in combination with a hyperbaric oxygen therapy device, or in an environment where combustible gas may be generated.
  • Page 6 • For the AC adapter connected to the unit, supplies, and optional devices, use only the standard accessories or OMRON-specified products. This may damage and/or may be hazardous to the device. • Do not use in a location with moisture, or a location where water may splash on the unit.
  • Page 7 Caution • Before using the unit, verify that none of the following apply to the - Poor peripheral circulation, noticeably low blood pressure, or low body temperature (there will be low blood flow to the measurement position) - The patient uses an artificial heart and lung (there will be no pulse) - The patient has a mastectomy or lymph node clearance - The patient has an aneurysm - The patient has frequent arrhythmia...
  • Page 8 Maintenance and inspection Warning • To use the unit safely and correctly, always inspect the unit when starting work. • Unauthorized modification is prohibited by law. Do not attempt to disassemble or modify the unit. Dry cell battery Warning • If battery fluid comes in contact with the eye, immediately flush with copious amounts of water.
  • Page 9 • Do not use the cuff if it is damaged or has holes. • Only an OMRON GS CUFF2 can be used with this device. The use of any other cuff may result in incorrect measurement.
  • Page 10 Note: Setup • Read and understand the manual for each optional accessory. This manual does not contain cautionary information for optional accessories. • Exercise caution with the cables and arrange so that the patient does not become entangled or bound. Before use / during use - No smoke, abnormal odor, or abnormal noise is emitted.

  • Page 11: Using The Unit Components Of The Product

    * UK 3-pin plug AC Adapter AC Adapter UK HHP-BFH01 (9546044-0) HXA-GCFM-PBE HXA-GCFS-PBE HXA-GCFSS-PBE (9546008-3) (9546007-5) (9546021-0) Caution • Only an OMRON GS CUFF2 can be used with this device. The use of any other cuff may result in incorrect measurement.

  • Page 12: Features Of The Product

    Features of the Product The blood pressure accuracy of the HBP-1120 is clinically proven. Easy to use, the HBP-1120 is intended for use by medical professionals. device indicates that “zero setting” was successful. alcohol. stops deflation for 5 seconds. pulse that may be caused by heart disease or other serious health...

  • Page 13: Features / Functions Of Unit

    Features / Functions of Unit Front and bottom of unit [Power ON/OFF] Turns the power ON/OFF. button [Auscultation] Press to enter “Auscultation Mode” button (page 19). Press to start blood pressure measurement. [START/STOP] While the cuff is inflating, hold down to button continuously inflate (page 18).
  • Page 14 LCD Display Displays systolic blood pressure. Displays diastolic blood pressure. PULSE Displays the pulse rate. Lights up in the measurement result display if the pulse wave interval was irregular Irregular pulse wave icon or there was body movement during measurement. Auscultation icon Lights up when “Auscultation Mode”...

  • Page 15: Installing The Batteries

    Installing the Batteries Warning • If battery fluid comes in contact with the eye, immediately flush with copious amounts of water. Do not rub. Seek medical attention immediately. • Do not throw into flame, disassemble, or heat. • Do not attempt to disassemble or modify the battery. •...

  • Page 16: Cuff Selection And Connection

    Cuff Selection and Connection Warning • If a cuff is used on a patient with an infection, treat the cuff as medical waste, or disinfect before reuse. Caution • Do not use the cuff if it is damaged or has holes. •...

  • Page 17: Applying The Cuff To The Patient

    Applying the Cuff to the Patient The device can be used on either the right or left arm. Wrap the cuff on a bare arm or over thin clothing. Thick clothing or a rolled up sleeve will cause inaccurate blood pressure measurements.
  • Page 18 Caution • Make sure the cuff is wrapped in the correct arm position and is at the same height as the heart. NOTE: • If measurement is difficult due to arrhythmia, use a different blood pressure measurement method. • If the patient has acute inflammation, a pyogenic ailment, or an external wound at the location where the cuff is to be wrapped, follow the instructions of the doctor.

  • Page 19: Zero Indicator Function

    Zero Indicator Function Before each measurement, this device indicates that “zero setting” was successful. setting” starts. When completed, appears. setting” takes place from the ready screen (which shows “0”). When completed, appears.

  • Page 20: Measurement In "Normal Mode

    Measurement in “Normal Mode” 1. Press the [START/STOP] button. Blood pressure measurement is performed once. 2. The measurement results are displayed. If a measurement value is outside the corresponding range below, the value will flash. If the cuff is not sufficiently inflated, it can be inflated manually. During inflation, hold down the [START/STOP] button to inflate continuously.

  • Page 21: Measurement In "Auscultation Mode

    Caution • The accuracy of a flashing measurement value that is outside the measurement range is not guaranteed. Always check the patient’s condition before deciding what steps to take. NOTE: • If inflation is insufficient, inflation may restart automatically while measurement is in progress.

  • Page 22: Stopping The Measurement

    Inflation starts. When the cuff is sufficiently inflated, deflation automatically starts. 4. At the SYS point that you determine by auscultation, press the [Auscultation] button. The first time you press the [Auscultation] button, the SYS value appears. 5. At the DIA point that you determine by auscultation, press the [Auscultation] button.

  • Page 23: Non-Invasive Pressure Measurement Principles

    Oscillometric method The beat in the pulsation generated by the contraction of the heart is captured as the pressure inside the cuff to measure the blood pressure. If the cuff wrapped around the upper arm is pressurized sufficiently, the blood flow stops, but the beat of the pulsation is present and the pressure inside the cuff receives this and oscillates.

  • Page 24: Maintenance

    Maintenance Maintenance Inspection and Safety Management The HBP-1120 must be maintained to ensure functionality and to secure the safety of patients and operators. Daily checks and maintenance should be performed by the operator.In addition, qualified personnel are necessary to maintain the performance and the safety, and to conduct periodic inspections.

  • Page 25: Check Before Use

    • The device is not making any unusual noises. • Press each button and check that it works. • Make sure that a suitable OMRON GS CUFF2 is attached (one that fits the circumference of the patient’s arm). • The cuff tube is firmly connected.

  • Page 26: Checking Pressure Accuracy

    Checking Pressure Accuracy You can check the pressure accuracy of the device. [Power ON/OFF] [START/STOP] button button [Auscultation] button 1. Make sure the power is on. “Zero setting” is performed. When “zero setting” is finished, the pressure accuracy verification screen appears. the pressure accuracy check.

  • Page 27: Troubleshooting

    AC adapter, remove the batteries, and contact your OMRON retail dealer or distributor. The unit display does not operate Cause / solution Stop using the unit and contact your OMRON retail dealer or distributor. The unit becomes hot Cause Solution...
  • Page 28 Measurement was not possible Cause / solution Check the patient by palpation or other method. After checking the patient, check the error code and see “List of Error Codes” (page 28) for Non Invasive Blood Pressure (NIBP) measurement. Cause / solution The causes below are possible.
  • Page 29 Cause Solution Deflates quickly Check for a loose cuff connection. Measure circumference of patient’s Incorrect cuff size used. arm and ensure correct sized cuff is used. Ensure cuff is applied to a bare Cuff wrapped over thick clothing. arm, or very thin clothing. Ensure patient is seated, feet flat Patient not seated properly.

  • Page 30: List Of Error Codes

    Description Points to check code The cuff tube is not connected Firmly connect the cuff tube. Replace with an OMRON GS Air is leaking from the cuff. CUFF2 that does not leak. Did not inflate properly because Have the patient not move...
  • Page 31 “Auscultation Mode” reaches the desired value. If this occurs during measurement, repeat measurement.If this occurs Over-inflation occurs when not performing measurement, contact your OMRON retail dealer or distributor. Replace with new batteries. The batteries are depleted. (page 13)

  • Page 32: Disposal

    Disposal As there is a risk of environmental pollution, follow your applicable national and local legal regulations regarding disposal or recycling of this equipment and batteries. The main constituents of each part are listed in the table below. As there is a risk of infection, do not recycle patient attachments such as cuffs, but dispose of them as instructed by your facility’s procedures and applicable regulations.
  • Page 33 Specifications Technical Specifications: HBP-1120 Main unit Product category Electronic Sphygmomanometers Product Automatic Upper Arm description Blood Pressure Monitor Model (code) HBP-1120 (HBP-1120-E) Measurement NIBP, PR Parameter Dimension Weight Display 7 segment LCD Protection Class 2 (AC adapter) Class Internal powered equipment (when operating with battery only)
  • Page 34 Operating Conditions Storage and transportation Measurement Oscillometric technology Measurement Dynamic Linear Deflation method method Pressure 0 to 300 mmHg display range Pressure display Within ±3 mmHg accuracy NIBP SYS 60 to 250 mmHg measurement DIA 40 to 200 mmHg range PULSE 40 to 200 /min Maximum mean error within ±5 mmHg NIBP accuracy...
  • Page 35 Manufacturer’s quality Metrology symbol control mark Symbol of Eurasian Date of manufacture Conformity Serial number Clinically validated Technology by OMRON LOT number Healthcare in Japan Unique device OFF/ON for a part of equipment Medical Device Direct current Need for the user to follow...
  • Page 36 Symbols description To indicate generally elevated, potentially hazardous, levels of non- ionizing radiation, or to indicate equipment or Indication of connector systems e.g. in the medical polarity electrical area that include RF transmitters or that intentionally apply RF electromagnetic energy for diagnosis or treatment.
  • Page 37 - During measurement, portable RF communications device (including peripherals such as antenna cables and external antennas) should be used no closer than 30 cm to any part of the monitor, including cables specified by OMRON. Otherwise, degradation of the performance of the monitor could result.

  • Page 38: Manufacturer's Declaration

    Manufacturer’s Declaration The HBP-1120 is intended for use in the electromagnetic environment specified below. The customer or the user of the HBP-1120 should assure that it is used in such an environment. Emission Test Compliance The HBP-1120 uses RF energy only for internal functions.
  • Page 39 25/30 cycles 25/30 cycles on power supply during power mains input lines interruptions, it is IEC 61000-4-11 recommended that the HBP-1120 be powered 0 % U 0 % U from an uninterruptible 250/300 cycles 250/300 cycles power supply or batteries.
  • Page 40 AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. strength in the location in which the HBP-1120 is used exceeds the applicable RF compliance level above, the HBP-1120 should be observed to verify normal operation.
  • Page 41 Test specifications for ENCLOSURE PORT IMMUNITY to RF Test Band Service Modulation Maximum Distance IMMUNITY frequency (MHz) power TEST LEVEL (MHz) (V/m) 380 to TETRA 400 Pulse modulation 18 Hz 430 to GMRS 460, FRS 460 ± 5 kHz deviation 1 kHz sine 704 to LTE Band 13,...
  • Page 44 Manufacturer OMRON HEALTHCARE Co., Ltd. 53, Kunotsubo, Terado-cho, Muko, KYOTO, 617-0002 JAPAN OMRON HEALTHCARE EUROPE B.V. Scorpius 33, 2132 LR Hoofddorp, THE NETHERLANDS www.omron-healthcare.com Importer in EU OMRON DALIAN Co., Ltd. No. 3, Song Jiang Road, Production facility Economic and Technical Development Zone,...

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