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INTRODUCTION

INTRODUCTION

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CAUTION

CAUTION

* This device is intended for adult use in homes only. 

* The device is not suitable for use on neonatal patients, pregnant women,patients with 

implanted, electronical devices, patients with pre-eclampsia, premature ventricular beats, 

atrial fibrillation, peripheral, arterial disease and patients undergoing intravascular therapy or 

arterio-venous shunt or people who received a mastectomy. Please consult your doctor prior 

to using the unit if you suffer from illnesses.

* The device is not suitable for measuring the blood pressure of children. Ask your doctor 

before using it on older children.

* The device is not intended for patient transport outside a healthcare facility.

* The device is not intended for public use.

* This device is intended for no-invasive measuring and monitoring of arterial blood 

pressure.It is not intended for use on extremities other than the arm or for functions other 

than obtaining a blood pressure measurement.

* Do not confuse self-monitoring with self-diagnosis. This unit allows you to monitor your 

blood pressure.Do not begin or end medical treatment without asking a physician for 

treatment advice.

* If you are taking medication,consult your physician to determine the most appropriate time 

to measure your blood pressure. Never change a prescribed medication without consulting 

your physician.

* Do not take any therapeutic measures on the basis of a self measurement. Never alter the 

dose of a medicine prescribed by a doctor. Consult your doctor if you have any question 

about your blood pressure.

* When the device is used to measure patients who have common arrhythmias such as 

atrial or ventricular premature beats or atrial fibrillation, the best result may occur with 

deviation. Please consult your physician about the result.

* Don't kink the connection tube during use, otherwise, the cuff pressure may continuously 

increase which can prevent blood flow and result in harmful injury to the PATIENT.

* When using this device, please pay attention to the following situation which may interrupt 

blood flow and influence blood circulation of the patient, thus cause harmful injury to the 

patient: connection tubing kinking too frequent and consecutive multiple measurements; the 

application of the cuff and its pressurization on any arm where intravascular access or 

therapy, or an arterio-venous (A-V) shunt, is present; inflating the cuff on the side of a 

mastectomy.

* Warning: Do not apply the cuff over a wound;otherwise it can cause further injury.

*Do not inflate the cuff on the same limb which other monitoring ME equipment is applied 

around simultaneously, because this could cause temporary loss of function of those 

simultaneously-used monitoring ME equipment.

*On the rare occasion of a fault causing the cuff to remain fully inflated during measurement, 

open the cuff immediately. Prolonged high pressure (cuff pressure 

 300mmHg or constant 

pressure 

 15mmHg for more than 3 minutes) applied to the arm may lead to an 

ecchymosis.

*Please check that operation of the device does not result in prolonged impairment of 

patient blood circulation.

* When measurement, please avoid compression or restriction of the connection tubing.

* The device cannot be used with HF surgical equipment at the same time.

* The ACCOMPANYING DOCUMENT shall disclose that the SPHYGMOMANOMETER 

was clinically investigated according to the requirements of ISO 81060-2:2013.

* To verify the calibration of the AUTOMATED SPHYGMOMANOMETER, please contact 

the manufacturer.

* This device is contraindicated for any female who may be suspected of, or is pregnant. 

Besides providing inaccurate readings, the effects of this device on the fetus are unknown.

* Too frequent and consecutive measurements could cause disturbances in blood 

circulation and injuries.

* This unit is not suitable for continuous monitoring during medical emergencies or 

operations.Otherwise, the patient’s arm and fingers will become anaesthetic, swollen and 

even purple due to a lack of blood.

* When not in use, store the device with the adapter in a dry room and protect it against 

extreme moisture, heat, lint, dust and direct sunlight. Never place any heavy objects on the 

storage case.

* This device may be used only for the purpose described in this booklet. The manufacturer 

cannot be held liable for damage caused by incorrect application.

*This device comprises sensitive components and must be treated with caution. Observe 

the storage and operating conditions described in this booklet.

* The equipment is not AP/APG equipment and not suitable for use in the presence of a 

flammable anesthetic mixture with air of with oxygen or nitrous oxide.

* Warning: No servicing/maintenance while the ME equipment is in use.

* The patient is an intended operator.

* The patient can measure, transmit data and change batteries under normal circumstances 

and maintain the device and its accessories according to the user manual.

* To avoid measurement errors, please avoid the condition of strong electromagnetic field 

radiated interference signal or electrical fast transient/burst signal.

* The blood pressure monitor, its adaptor, and the cuff are suitable for use within the patient 

environment. If you are allergic to polyester, nylon or plastic, please don't use this device. 

* During use, the patient will be in contact with the cuff. The materials of the cuff have been 

tested and found to comply with requirements of ISO 10993-5:2009 and ISO 

10993-10:2010. It will not cause any potential sensation or irritation reaction.

* Adaptor is specified as a part of ME EQUIPMENT.

* If you experience discomfort during a measurement, such as pain in the arm or other 

complaints, press the START/STOP button to release the air immediately from the cuff. 

Loosen the cuff and remove it from your arm.

* If the cuff pressure reaches 40 kPa (300 mmHg), the unit will automatically deflate. 

Should the cuff not deflate when pressure reaches 40 kPa (300 mmHg), detach the cuff 

from the arm and press the START/STOP button to stop inflation.

* Before use, make sure the device functions safely and is in proper working condition. 

Check the device, do not use the device if it is damaged in any way. The continuous use of 

a damaged unit may cause injury, improper results, or serious danger.

* Do not wash the cuff in a washing machine or dishwasher!

Summary of Contents for TMB-1872-B

Page 1: ...e Monitor TMB 1872 B Please read the user manual carefully and thoroughtly so as to ensure the safe usage of this product Keep the manual well for further reference in case you have problems Guangdong...

Page 2: ...he Records INFORMATION FOR USER 21 Tips for measurement Maintenances ABOUT BLOOD PRESSURE 23 What are systolic pressure and diastolic pressure What is the standard blood pressure classification Irregu...

Page 3: ...rinciple Contraindications 1 The device should not be used by any person who may be suspected of or is pregnant 2 The device is not suitable for use on patients with implanted electrical devices such...

Page 4: ...oes not result in prolonged impairment of patient blood circulation When measurement please avoid compression or restriction of the connection tubing The device cannot be used with HF surgical equipme...

Page 5: ...neously Cleaning Dust environment may affect the performance of the unit Please use the soft cloth to clean the whole unit before and after use Don t use any abrasive or volatile cleaners The device d...

Page 6: ...ies 2 Installing and Replacing the Batteries CAUTION CAUTION Replace the batteries whenever the below happens The shows The display is dim The display does not light up Do not use new and used batteri...

Page 7: ...hen press SET button for 3 seconds to enter the mode for year setting 3 When you get the right year press SET button to set down and turn to next step 4 Repeat steps 2 and 3 to set the MONTH and DAY 5...

Page 8: ...connect with your smartphone on the app to continute the pair up Bluetooth Module No LS8261 RF Frequency Range 2400 MHz to 2483 5 MHz Output Power Range 8dBm Supply Voltage 1 9 3 6 V Transmitting Dist...

Page 9: ...asurements at approximately the same time on the same arm or as directed by a physician 5 6 Take the measurement in a silent room The cuff should maintain at the same level as the right atrium of the...

Page 10: ...mbol will not blink then the device will turn off 1 When the monitor is off press Start Stop button to turn on the monitor and it will finish the whole measurement Adjust the zero LCD display Inflatin...

Page 11: ...ed from the list The corresponding time is 10 38 The corresponding date is 2019 year July 1st CAUTION The date and time of the record will be shown alternately The current No is No 1 three records in...

Page 12: ...smoking When talking or moving your fingers When you want to discharge urine 1 Hold pressing MEM button for 3 seconds when the monitor is in the memory recall mode the flash display dEL ALL User ID w...

Page 13: ...usable cuff with water and never immerse the cuff in water An irregular heartbeat is detected when a heartbeat rhythm varies while the device is measuring systolic pressure and diastolic pressure Duri...

Page 14: ...his section includes a list of error messages and frequently asked questions for problems you may encounter with your blood pressure monitor If the products not operating as you think it should check...

Page 15: ...protection Protection against ingress of water Software Version A01 Pressure 5 C 40 C within 3mmHg 0 4kPa Pulse value 5 Device Classification Battery Powered Mode Internally Powered ME Equipment AC Ad...

Page 16: ...Biological evaluation of medical devices Part 10 Tests for irritation and skin sensitization EN ISO 15223 1 2016 ISO 15223 1 2016 Medical devices Symbols to be used with medical device labels labellin...

Page 17: ...hat supplies buildings used for domestic purposes Guidance and manufacturer s declaration electromagnetic immunity Immunity test 8 kV contact 15 kV air 8 kV contact 15 kV air 2 kV power supply lines l...

Page 18: ...te for the frequency of the transmitter Recommended separation distances d 0 35 d 1 2 10V m 80 Am at 1kHz 80 MHz to 800 MHz d 1 2 800 MHz to 2 7 GHz d 2 3 where P is the maximum output power rating of...

Page 19: ...960 GSM 800 900 TETRA 800 iDEN 820 CDMA 850 LTE Band 5 Pulse modulation b 18Hz 2 0 3 28 1720 1845 1970 1700 1990 GSM 1800 CDMA 1900 GSM 1900 DECT LTE Band 1 3 4 25 UMTS Pulse modulation b 217Hz 2 0 3...

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