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13 

PM-1794-01-06/2018 

 

  

Cautions 

• Do not install the unit in the following locations: 
- Locations with dust, salt, or sulfur. 
- Locations directly exposed to sunlight for extended periods of time (in particular, do 
not leave in direct sunlight or near a source of ultraviolet light for extended periods, 
as ultraviolet light will cause deterioration of the LCD). 
- Locations subject to vibration or shock. 
- Near heaters. 
• Do not use in a location with noise-emitting equipment such as a room with MRI, 
CT, X-ray or HF surgical equipment or an operating room. Noise from the equipment 
may interfere with the operation of the unit. 

 

Before use / during use  

 
Warnings 

• The unit complies with the EMC (Electro Magnetic Compatibility) standard 
(IEC60601-1-2). As such, it can be used simultaneously with multiple medical 
instruments. However, if instruments that generate noise such as an electric scalpel 
or a microwave therapy device are near the unit, check the operation of the unit 
during and after use of these instruments. 
• If an error occurs or a measurement result is questionable, check the vital signs of 
the patient by auscultation or palpation. Avoid relying solely on the measurement 
results of the unit when judging the patient's condition. 
• Only trained healthcare providers should use this device. Do not allow patients to 
operate this device. 
• Properly connect the connectors and AC adapter cable. 
• Do not place objects or liquids on top of this unit. 
• Check the following before using the unit: 
- Make sure the AC adapter cable is not damaged (wires are not exposed or broken), 
and the connections are firm. 
• 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. 
• This unit is intended for use in physicians' office, hospitals, clinics and other medical 
facilities. 
• Do not use the unit if it emits smoke, an abnormal odor, or abnormal noise. 
• Do not bring cellular telephones or transceivers into the room where the unit is 
installed or being used. 
• Do not connect multiple monitors to the same patient. 
• Do not connect the unit to a power outlet that is controlled by a wall switch. 

 

Cautions 

• Before using the unit, verify that none of the following apply to the patient: 
- Poor peripheral circulation, noticeably low blood pressure, or low body temperature 
(there will be low blood flow to the measurement position) 

Summary of Contents for HBP-1120

Page 1: ...1 0 23 55 44 701 www omron healthcare com BANKERS BANK OF TOKYO MITUSBISHI HOLLAND N V ACC NR 063 56 15 320 IBAN NL95BOTK0635615320 SWIFT BOTKNL2X CHAMBER OF COMMERCE NR 342 10306 BTW VAT NR NL8132 86...

Page 2: ...el code HBP 1120 HBP 1120 E LEGAL MANUFACTURER OMRON HEALTHCARE Co Ltd 53 Kunotsubo Terado cho Muko KYOTO 617 0002 Japan PRODUCION FACILITY OMRON DALIAN Co Ltd No 3 Song Jiang Road Economic and Techni...

Page 3: ...HXA GCFXL PBE AC Adapter HHP CM01 HHP CM01 E AC Adapter UK HHP BFH01 HHP BFH01 E General description OMRON s HBP 1120 HBP 1120 E blood pressure monitor is a professional medical device meant for meas...

Page 4: ...for use This device is a digital monitor intended for use in measuring blood pressure and pulse rate in adult patient population Measurement Parameter Non Invasive Blood Pressure Pulse rate Features...

Page 5: ...a bare arm or over thin clothing 3 Select the mode of application Normal Mode Auscultation Mode 4 Press start 5 Note the blood pressure and pulse rate in the patients documents Review the Instruction...

Page 6: ...104 F Humidity range 15 to 85 RH not condensed Atmospheric pressure 700 to 1060hPa Storage and transportation Temperature range 20 to 60 C 4 to 140 F Humidity range 10 to 95 RH not condensed Atmosphe...

Page 7: ...rdboard Instruction Manual Paper Materials used for accessories Cuff Item Material Outside cloth Nylon Polyester Inner cloth Polyester Air bag Flexible urethane sheet Velcro tape hook Nylon Velcro tap...

Page 8: ...8 PM 1794 01 06 2018 Title page of Instruction Manual...

Page 9: ...9 PM 1794 01 06 2018 Unfolded package design of main device and accessories Main device Information in white square on package artwork...

Page 10: ...10 PM 1794 01 06 2018 AC adapter HHP CM01 AC Adapter with UK plug HHP BFH01...

Page 11: ...EN 1060 3 1997 A2 2009 EN 60601 1 2006 A1 2013 EN 60601 1 6 2010 A1 2015 EN 80601 2 30 2010 A1 2015 EN 62304 2006 A1 2015 EN 62366 2008 A1 2015 EN ISO 10993 1 2009 AC 2010 EN ISO 10993 5 2009 EN ISO...

Page 12: ...oxygen therapy device or in an environment where combustible gas may be generated Do not use in combination with magnetic resonance imaging MRI equipment If MRI is to be performed remove cuff connect...

Page 13: ...he measurement results of the unit when judging the patient s condition Only trained healthcare providers should use this device Do not allow patients to operate this device Properly connect the conne...

Page 14: ...en cleaning the unit turn off the power and disconnect the AC adapter from the unit After cleaning the unit make sure it is completely dry before connecting to a power outlet Do not spray pour or spil...

Page 15: ...on wrap the cuff as indicated in the cautionary points in this manual Do not connect the NIBP cuff or cuff joint to a luer lock adapter Do not bend cuff tube during inflation and deflation particularl...

Page 16: ...easurement Disposal As there is a risk of environmental pollution follow your applicable national and local legal regulations regarding disposal or recycling of this equipment The main constituents of...

Page 17: ...utor Servicing 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 q...

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