OU9TMB1491-BBlood Pressure Monitor

version:1.0 User Manual Blood Pressure Monitor TMB-1491-BT Arm Type Thank you very much for selecting TRANSTEK Blood Pressure MonitorTMB-1491-BT.Please do read the user manual carefully and thoroughtly so as t o ensure the safe usage of this product, and keep the manual well f or further reference in case you have problems. Guangdong Transtek Medical Electronics Co., Ltd. Zone A, No.105 ,Dongli Road, Torch Development District, Zhongshan,528437,Guangdong,China  Table of Contents CATALOGUE CATALOGUE INTRODUCTION....................................... ................................................... .........................2 General DescriptionIndications for UseSafety InformationLCD Display SignalMonitor Components BEFORE YOU START........................................ ................................................... ................6 The Choice of Power SupplyInstalling and Replacing the BatteriesMeasurement PrincipleSetting Date, Time and Measurement UnitSelect the UserPair-up the Blood Pressure Monitor with Your Device MEASUREMENT............................................... ................................................... .................13 Tie the CuffStart the Measurement DATA MANAGEMENT....................................... ................................................... ................16 Recall the RecordsDelete the Records INFORMATION FOR USER................................. ................................................... ............18 Tips for measurementMaintenances ABOUT BLOOD PRESSURE...................................... ................................................... .....20 What are systolic pressure and diastolic pressure?What is the standard blood pressure classification?Why does my blood pressure fluctuate throughout the day?Why do I get a different blood pressure at home compared to t he hospital? Is the result the same if measuring on the right arm? TROUBLESHOOTING....................................... ................................................... ..............22 SPECIFICATIONS........................................ ................................................... ...................23 AUTHORIZED COMPONENT .................................. ................................................... ......24 CONTACT INFORMATION................................ ................................................... ..............24 COMPLIED STANDARDS LIST.................................. ................................................... .....25 FCC STATEMENT.......................................... ................................................... ..................26 EMC GUIDANCE......................................... ................................................... ....................27   INTRODUCTION INTRODUCTION Safety Information The signs below might be in the user manual, labeling or o ther component. They are the requirement of standard and using. Symbol for “THE OPERATION GUIDE MUST BE READ” Symbol for “MANUFACTURER”Symbol for “SERIAL NUMBER” Symbol for “TYPE BF APPLIED PARTS” Symbol for “DIRECT CURRENT” Symbol for “ENVIRONMENT PROTECTION - Electrical waste products should not be disposed of with household waste. Please recycle where facilities exist. Check with your local authority or retailer for recycling advice” Symbol for “MANUFACTURE DATE” Thank you for selecting TRANSTEK arm type blood pressure Monitor (TMB-1491-BT). The monitor features blood pressure measurem ent, pulse rate measurement and the result storage. The design prov ides you with two years of reliable service. Readings taken by the TMB-1491-BT are equivalent to those o btained by a trained observer using the cuff and stethoscope ausculta tion method. This manual contains important safety and care information , and provides step by step instructions for using the product. Read the manual thoroughly before using the product. Features: Maximum 60 records General Description For indoor use only F1 7$9ĭ &&& Symbol for “Class II Equipment” 3rd technonoly: Measuring during inflation (The updated technology in the world) 60mm×40.5 mm Digital LCD display The Bluetooth Combination Mark Symbol for “Including RFtransmitter” This device is intended for adult use only.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 funct ions 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 consu lting your Physician. When the device was used to measure patients who have common arrh ythmias such as atrial or ventricular premature beats or atrial fibrillation, the best resu lt may occur with deviation. Please consult your physician about the result.If the cuff pressure exceeds 40 kPa (300 mmHg), the unit will aut omatically deflate. Should the cuff not deflate when pressures exceeds 40 kPa (300 mmHg), detach the cuff f rom the arm and press the START/STOP button to stop inflation.The equipment is not AP/APG equipment and not suitable fo r use in the presence of a flammable anesthetic mixture with air of with oxygen or nitrous oxide.The operator shall not touch output of batteries/AC adapt or and the patient simultaneously. To avoid measurement errors, please avoid the condition of strong electromagnetic field radiated interference signal or electrical fast transient/burst signal.The user must check that the equipment functions safely and see that it is in proper working condition before being used.This device is contraindicated for any female who may be suspected of, or is pregnant. Besides providing in…

Text truncated - open the document above for the full version.

External Photo of TMB-1491-BT

Dimension：49.70X19.70mm,Thickness：0.2mm label TMB-1491-BT Colour：black text with silver background Material：adhesive label with water proof TMB-1491-BT Model IP Classification:IP21 Rating: 4×AAA alkaline batteries, 6V AC adaptor powered mode: 6V 1A (Can be supplied by AC adaptor model KH0601000UW!) FCC ID: OU9TMB1491-B FCC STATEMENT: This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions:(1) this device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation. 2015-07 Guangdong Transtek Medical Electronics Co., Ltd. Zone A, No.105 ,Dongli Road, Torch Development District, Zhongshan,528437,Guangdong,China TMB-1491-BT Model IP Classification:IP21 SN Rating: 4×AAA alkaline batteries, 6V AC adaptor powered mode: 6V 1A (Can be supplied by AC adaptor model KH0601000UW!) FCC ID: OU9TMB1491-B FCC STATEMENT: This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions:(1) this device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation. 2015-07 Guangdong Transtek Medical Electronics Co., Ltd. Zone A, No.105 ,Dongli Road, Torch Development District, Zhongshan,528437,Guangdong,China SN

Internal Photo of TMB-1491-BT

TÜV SÜD Certification and Testing (China) Co., Ltd. Shenzhen Branch Building 12&13, Zhiheng Wisdomland Business Park, Nantou Checkpoint Road 2, Nanshan District, Shenzhen City, 518052, P. R. China Tel. +86 755 8828 6998, Fax: +86 755 8828 5299 RF exposure Estimation 1. Introduction The EUT is Blood Pressure Monitor, which contain Bluetooth function inside. 2. Limit and Guidelines on Exposure to Electromagnetic Fields According to§15.247(e)(i) and §1.1307(b)(1), systems operating under the provisions of this section shall be operated in a manner that ensure that the public is not exposed to radio frequency energy level in excess of the Commission’s guideline. According to KDB 447498 D01 Mobile Portable RF Exposure v05r01, no SAR required if power is lower than the flowing threshold: The 1-g and 10-g SAR test exclusion thresholds for 100 MHz to 6 GHz at test separation distances ≤ 50 mm are determined by: [(max. power of channel, including tune-up tolerance, mW)/(min. test separation distance, mm)] [√f(GHz)] ≤ 3.0 for 1-g SAR and ≤ 7.5 for 10-g extremity SAR, where • f(GHz) is the RF channel transmit frequency in GHz • Power and distance are rounded to the nearest mW and mm before calculation25 • The result is rounded to one decimal place for comparison • 3.0 and 7.5 are referred to as the numeric thresholds in the step 2 below The test exclusions are applicable only when the minimum test separation distance is ≤ 50 mm and for transmission frequencies between 100 MHz and 6 GHz. When the minimum test separation distance is < 5 mm, a distance of 5 mm according to 5) in section 4.1 is applied to determine SAR test exclusion. 3. Calculation method [(max. power of` channel, including tune-up tolerance, mW)/(min. test separation distance, mm)] ·[√f(GHz)] ≤ 3.0 BT4.0： Conducted Power + tune up tolerance = -0.39dBm=0.9 mW Distance = 5 mm f = 2.402 GHz [0.9/5] * SQRT(2.402) =0.28 0.28 ≤ 3.0 Therefore, excluded from SAR testing. TÜV SÜD Certification and Testing (China) Co., Ltd. Shenzhen Branch eviewed by: Prepared By: Phoebe Hu/EMC Project Manager Felix Li/EMC Project Engineer Date: 2015-11-02 Date: 2015-11-02

Report Number: 68.930.15.037.01 EMC_SZ_FR_21.00 FCC Release 2014-03-20 TÜV SÜD Certification and Testing (China) Co., Ltd. Shenzhen Branch Building 12&13, Zhiheng Wisdomland Business Park, Nantou Checkpoint Road 2, Nanshan District, Shenzhen City, 518052, P. R. China Tel. +86 755 8828 6998, Fax: +86 755 8828 5299 Page 1 of 27 FCC- TEST REPORT Report Number : 68.930.15.037.01 Date of Issue: October 10, 2015 Model : TMB-1491-BT Product Type : Blood Pressure Monitor Applicant : Guangdong Transtek Medical Electronics Co., Ltd Address : Zone A, No. 105 Dongli Road, Torch Development District, 528437 Zhongshan, Guangdong, PEOPLE'S REPUBLIC OF CHINA Production Facility : Guangdong Transtek Medical Electronics Co., Ltd Address : Zone B, No. 105 Dongli Road, Torch Development District, 528437 Zhongshan, Guangdong, PEOPLE'S REPUBLIC OF CHINA Test Result :  Positive  Negative Total pages including Appendices : 27 TÜV SÜD Certification and Testing (China) Co., Ltd. Shenzhen Branch is a subcontractor to TÜV SÜD Product Service GmbH according to the principles outlined in ISO 17025. TÜV SÜD Certification and Testing (China) Co., Ltd. Shenzhen Branch reports apply only to the specific samples tested under stated test conditions. Construction of the actual test samples has been documented. It is the manufacturer's responsibility to assure that additional production units of this model are manufactured with identical electrical and mechanical components. The manufacturer/importer is responsible to the Competent Authorities in Europe for any modifications made to the production units which result in non-compliance to the relevant regulations. TÜV SÜD Certification and Testing (China) Co., Ltd. Shenzhen Branch shall have no liability for any deductions, inferences or generalizations drawn by the client or others from TÜV SÜD Certification and Testing (China) Co., Ltd. Shenzhen Branch issued reports. This report is the confidential property of the client. As a mutual protection to our clients, the public and ourselves, extracts from the test report shall not be reproduced except in full without our written approval. Report Number: 68.930.15.037.01 EMC_SZ_FR_21.00 FCC Release 2014-03-20 TÜV SÜD Certification and Testing (China) Co., Ltd. Shenzhen Branch Building 12&13, Zhiheng Wisdomland Business Park, Nantou Checkpoint Road 2, Nanshan District, Shenzhen City, 518052, P. R. China Tel. +86 755 8828 6998, Fax: +86 755 8828 5299 Page 2 of 27 1 Table of Contents 1 Table of Contents ................................................................................................................................................................ 2 2 Details about the Test Laboratory ..................................................................................................................................... 3 3 Description of the Equipment under Test ........................................................................................................................ 4 4 Summary of Test Standards .............................................................................................................................................. 5 5 Summary of Test Results ................................................................................................................................................... 6 6 General Remarks ................................................................................................................................................................ 7 7 Test Setups .......................................................................................................................................................................... 8 8 Systems test configuration ................................................................................................................................................. 9 9 Technical Requirement ........................................................................................................................................................ 10 9.1 Conducted Emission.................................................................................................................................................... 10 9.2 Conducted peak output power................................................................................................................................ 13 9.3 6dB bandwidth .......................................................................................................................................................... 14 9.4 Power spectral density ............................................................................................................................................. 16 9.5 Spurious RF conducted emissions ........................................................................................................................ 17 9.6 Band edge ................................................................................................................................................................. 21 9.7 Spurious radiated emissions for transmitter ......................................................................................................... 23 10 Test Equipment List ...................................................................................................................................................... 26 11 System Measurement Uncertainty ............................................................................................................................. 27 Report Number: 68.930.15.037.01 EMC_SZ_FR_21.00 FCC Release 2014-03-20 TÜV SÜD Certification and Testing (China) Co., Ltd. Shenzhen Branch Building 12&13, Zhiheng Wisdomland Business Park, Nantou Checkpoint Road 2, Nanshan District, Shenzhen City, 518052, P. R. China Tel. +86 755 8828 6998, Fax: +86 755 8828 5299 Page 3 of 27 2 Details about the Test Laboratory Details about the Test Laboratory Tes…

Text truncated - open the document above for the full version.

Page 1 of 2 Test setup photos Conducted emission (150 kHz-30MHz) Transmitting spurious emission (below 1GHz) Page 2 of 2 Transmitting spurious emission (Above 1GHz)