nubeca BW2110 Instruction Manual Download Page 9

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Warranty Information

Periodical check:

Sensitive measuring devices must be checked from time to time for accuracy 

and leakage, we therefore recommend that the performance should be checked 

every 2 years and after maintenance and repair.
Please contact the local distributor for details. 

The unit satisfies the requirements of EN60601-1

 Medical electrical 

equipment Part 1: General requirements for basic safety and essential 
performance; EN60601-1-2: Medical electrical equipment Part 1-2:General 
requirements for basic safety and essential performance – Collateral standard: 
Electromagnetic compatibility – Requirements and tests; 
EN1060-1:Non-invasive sphygmomanometers – Part 1: General requirements;
EN1060-3: Non-invasive sphygmomanometers – Part 3: Supplementary 
requirements for electro-mechanical blood pressure measuring system.

EN1060-4

Non-invasive sphygmomanometers – Part 4: Test procedures 

to determine the overall system accuracy of automated non-invasive 
sphygmomanometers.

Warning: Do not use luer lock connector in the  construction of tubing. There
Is a possibility that they might be inadvertently connected to intravascular fluid 
systems, allowing air to be pumped into a blood vessel.

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Warranty Information

It can’t be used while the wrist (arm) has bleeding or wound to avoid the blood 
flowing from the wound in pressurizing.
It can’t be used while the wrist (arm) has bleeding or wound to avoid the blood 
flowing from the wound in pressurizing.

WARNING: No modification of this equipment is allowed.

Clean the cuff with a soft dry cloth.

Applied parts contains cuff.
The device

accessories and the packaging have to be disposed of waste 

correctly at the end of the usage. Please follow Local Ordinances or 
Regulations for disposal.

Protection Class: Internally powered equipment 
Applied Part Type: Type B
Moisture Protection: IPX0, continue operation

Manufacturer will make available on request circuit diagrams, component 

part lists etc for the service personnel in parts repair.

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Guidance and manufacture’s declaration – electromagnetic emission

Emission test

RF emission

Harmonic

Voltage

Group 1

Class B

Not applicable

Not applicable

The Digital Blood Pressure Monitor use RF energy only for 

its internal function. Therefore, its RF emissions are very low 

and are not likely to cause any interference in nearby 

electronic equipment.

The Digital Blood Pressure Monitor is suitable for use in all 

establishments other than domestic and those directly 

connected to the public low-voltage power supply network 

that supplies buildings used for domestic purposes.

CISPR 11

RF emissions

emissions

fluctuations/ 

flicker emissions

IEC 61000-3-3

IEC 61000-3-2

CISPR 11

Compliance

Electromagnetic environment – guidance

The Digital Blood Pressure Monitor is intended for use in the electromagnetic environment 

specified below. The customer of the user of the Digital Blood Pressure Monitor should 

assure that it is used in such an environment.

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Warranty Information

                              Guidance and manufacture’s declaration

Caution: this machine should not be used adjacent to or stacked with other 
equipment and that if adjacent or stacked use is necessary, this machine 
should be observed to verify normal operation in the configuration in which it 
will be used.
*MEDICAL ELECTRICAL EQUIPMENT needs special precautions regarding 
EMC and needs to be installed and put into service according to the EMC 
information provided in the ACCOMPANYING DOCUMENTS.
*Portable and mobile RF communications equipment can affect MEDICAL 
ELECTRICAL EQUIPMENT.
* Do not use a mobile phone or other devices that emit electromagnetic fields, 
near the unit. This may result in incorrect operation of the unit.
Caution: This unit has been thoroughly tested and inspected to assure proper 
performance and operation!
WARNING:
The use of ACCESSORIES, transducers and cables other than those specified, 
with the exception of transducers and cables sold by the MANUFACTURER of 
the COMPRESSOR NEBULIZER as replacement parts for internal 
components, may result in increased EMISSIONS or decreased IMMUNITY of 
the ME EQUIPMENT or ME SYSTEM.

Warranty Information

Summary of Contents for BW2110

Page 1: ...ttery lnstallation Replacement 8 9 Adjusting Settings 10 Proper Way of Measurement 11 Take a Measurement 12 13 Use the Memory Function To read the average value 14 To read the measurement value 15 To...

Page 2: ...RER SERIAL NUMBER The marking of electrical and electronics devices according to Directive 2002 96 EC The device accessories and the packaging have to be disposed of waste correctly at the end of the...

Page 3: ...ol smoking exercising and bathing for 30 minutes before taking a measurement 2 Stress raises blood pressure Avoid taking measurements during stressful times 3 The cuff can be applied to your left or r...

Page 4: ...Then press the MEM up button to change the current unit Press the START STOP button to save the current setting and turn off 11 Proper Way of Measurement 1 Wrap the cuff tightly around your wrist by...

Page 5: ...and pulse rate in the memory after completing a measurement every time It can automatically store 60 sets of measurement values The oldest record is deleted to save the latest measurement value when...

Page 6: ...on s systolic and diastolic pressures fall into different categories the higher category should apply WHO 80 85 90 100 110 Diastolic Blood Pressur mmHg 120 130 140 160 180 Systolic Blood Pressure mmHg...

Page 7: ...rs on the display screen No power Causes and Solutions Problem Eliminate Fault Replace both of the worn batteries with two new ones 23 Care and Maintenance Care Avoid subjecting the monitor to strong...

Page 8: ...operations A transportation fee or freight fee that may be incurred will be the owner s responsibility Any defect resulting from natural causes e g flood hurricane etc is not within this guarantee Thi...

Page 9: ...vice personnel in parts repair 32 Guidance and manufacture s declaration electromagnetic emission Emission test RF emission Harmonic Voltage Group 1 Class B Not applicable Not applicable The Digital B...

Page 10: ...r in the vicinity of equipment marked with the following symbol NOTE 1 At 80 MHz and 800 MHz the higher frequency range applies NOTE 2 These guidelines may not apply in all situations Electromagnetic...

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