Transtek Medical Electronics AW8001-LS Bluetooth Module with Body Pressure Monitor as host User Manual tmb 1014 bt
Guangdong Transtek Medical Electronics Co.,Ltd Bluetooth Module with Body Pressure Monitor as host tmb 1014 bt
Contents
User Manual
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| Document ID | 2475357 |
| Application ID | vv5sMLwtwQ+Mt22zJHuSHw== |
| Document Description | User Manual |
| Short Term Confidential | No |
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| Document Type | User Manual |
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| Filesize | 418.01kB (5225146 bits) |
| Date Submitted | 2014-12-17 00:00:00 |
| Date Available | 2014-12-18 00:00:00 |
| Creation Date | 2013-04-08 13:42:57 |
| Producing Software | Adobe PDF library 9.90 |
| Document Lastmod | 2014-12-01 15:21:45 |
| Document Title | tmb-1014-bt说明书 |
| Document Creator | Adobe Illustrator CS5 |
Version:1.0 User Manual Blood Pressure Monitor LS808-B Arm Type Contains FCC ID: OU9AW8001-LS GUANGDONG TRANSTEK MEDICAL ELECTRONICS CO., LTD Zone A, 5/F., Investment Building, No. 12, Huizhan East Rd., Torch Development District, Zhongshan, Guangdong, 528437, China Thank you very much for selecting TRANSTEK Blood Pressure Monitor LS808-B. Please do read the user manual carefully and thoroughly so as to ensure the safe usage of this product, and keep the manual well for your further reference in case you have problems. TABLE OF CONTENTS Table of Contents INTRODUCTION ............................................................. 2 General Description Indications for Use Measurement Principle Safety Information LCD Display Signal Monitor Components BEFORE YOU START ........................................................7 Power Supply and Charge Power Setting the Time,Date and Unit Pair up with Your Device Tie the Cuff MEASUREMENT .............................................................14 Start Measurement Data Management ........................................................... 16 Recall the Records Delete the Records INFORMATION FOR USER .....................................................20 Tips for Measurement Maintenance ABOUT BLOOD PRESSURE....................................................22 What are systolic pressure and diastolic pressure? What is the standard blood pressure classification? Why does my blood pressure fluctuate throughout the day? Why the blood pressure I get from the hospital is different from home? If the result is the same if measuring on the right arm? TROUBLESHOOTING .........................................................24 SPECIFICATIONS ............................................................. 25 ATHORIZED COMPONENT ............................................... 26 CONTACT INFORMATION...................................................... 26 COMPLIED STANDARDS LIST ............................................... 27 FCC STATEMENT ...... ...................................................... 28 EMC GUDIANCE ...... ...................................................... 29 INTRODUCTION INTRODUCTION General Description * Thank you for selecting TRANSTEK Blood pressure Monitor (LS808-B). The monitor features blood pressure measurement, pulse rate measurement and the result storage. The design provides you with two years of lifetime. * This manual contains important safety information and caution, and provides step by step instructions for using the product. * Please do read this user manual carefully and thoroughly before use. FEATURES: 86.1mm×24mm Blue LCD Display with White Backlight Measure-during-inflating Technology Up to 60 pieces of record stored Indications for Use 1.The Transtek Blood Pressure Monitor is digital monitors intended for use in measuring blood pressure and hearbeat rate with arm circumference ranging from 22cm to 42 cm (about 9-17 inches). 2. The monitor detects the appearance of irregular heartbeats during measurement and gives a warning signal with readings. 3. It is intended for adult use in the home/ domestic setting only. Contraindications 1. This device is contraindicated for any person who is connected to a wearable or implantable electronic device or instrument such as a pacemaker or defibrillator. 2. This device is not intended to be a diagnostic device. Contract your physician if hypertensive values are indicated. Measurement Principle This product uses the Oscillometric Measuring Method to detect blood pressure. Before every measurement, the unit establishes a “zero point” equivalent to the atmospheric pressure. Then it starts inflating the cuff. Meanwhile, the unit detects pressure oscillation generated by beat-to-beat pulsatile, which is used to determine the systolic pressure and diastolic pressure as well as pulse rate. The device also compares the longest and the shortest intervals of detected pulse wave to with the average value, and then calculates the standard deviation. The monitor will light up a warning symbol when the calculated standard deviation is larger than or equal to 15. Safety Information The below signs might be in the user manual, labeling or other components. They are the requirement of standard and using. Symbol for “TYPE BF APPLIED PARTS” Symbol for “THE OPERATION GUIDE MUST BE READ” Symbol for “ENVIRONMENT PROTECTION - Wast electrical 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” Symbol for “MANUFACTURER” Symbol for “DIRECT CURRENT” Symbol for “SERIAL NUMBER” The Bluetooth Combination Mark Symbol for “ Class II Equipment” F1 T1A/250V Φ3.6*10CCC Symbol for indoor use only Symbol for “Including RF transmitter” INTRODUCTION CAUTION 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 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 based solely 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. When the device was used to measure patients who have common arrhythmias such as atrial or ventricular premature beats or artrial fibrillation, the best result may occure deviation. Please consult your physician about the result. If the cuff pressure exceeds 40 kPa (300 mmHg), the unit will automatically deflate. Should the cuff not deflate when pressures exceeds 40 kPa (300 mmHg), detach the cuff from the arm and press the START/STOP button to stop inflation. 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. The operator shall not touch output of batteries/adaptor 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 provided inaccurate readings, the affects of this device on the fetus are unknown. Manufacturer will make available on request circuit diagrams, component parts list etc. 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. Please use the device under the environment which was provided in the user manual. Otherwise, the performance and lifetime of the device will been impacted and reduced. During using, the patient will 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 sensization or irritation reaction. The patient is an intended operator. The patient can measure, transmit data and charge battery under normal circumstances and maintain the device and its accessories according to the user manual. The blood pressure monitor, its adaptor, and the cuff are suitable for use within the patient environment. If you are allergic to dacron or plastic, please don’t use this device. Please keep the unit out of reach of infants, children or pets, since inhalation or swallowing of small parts is dangerous or even fata. The adaptor is specified as a part of ME equipment. If Luer lock connectors are used 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. The device is not suitable for public use. The device is not intended for PATIENT transport outside a healthcare facility. This device cannot be used with HF surgical equipment at the same time. Be careful to strangulation due to cables and hoses, particularly due to excessive length. INTRODUCTION LCD Display Signal Systolic Blood Pressure High blood pressure Diastolic Blood Pressure Low blood pressure Pulse beat/minute Low Battery Low battery and please charge the power. Unit Measurement unit of blood pressure IHB Detector Data pending to transmit Data transmitting Irregular Heartbeat Detector Measurement data stored in the device Data transmission succeeds. Memory Query Recalling the history records User ID Start measurement for selected user, and transmit the measuring result Current time Year/Month/Day(Hour:Minute) Shocking reminder Shocking will result in inaccurate Heartbeat Heartbeat Detection during the measurement INTRODUCTION BEFORE YOU START Power Supply and Charge Power Monitor Components DC POWER SOCKET ON/OFF BUTTON 1. The battery of LS808-B is built-in rechargeable li-polymer battery, the battery current is 1000 mAh. 2. Please use the AC adaptor to charge the battery, just like the following picture: SYSTOLIC PRESSURE DIASTOLIC PRESSURE QUERY/UP BUTTON PULSE RATE AC adaptor USER 1/SET BUTTON USER 2/ACTIVATION BUTTON Component list of pressure measuring system 1 PCBA 2 Air pipe 3 Pump 4 Valve 5 Cuff When powering on the monitor, the LCD doesn’t light up. CUFF (Type BF applied part) 2.AC Adaptor ( Model: UE08WCP- 060100SPA) 4. Cuff (22-42cm) (Type BF Applied Part) 3.User Manual displays on the LCD The LCD display dims List 1.Blood Pressure Monitor (LS808-B) Charging the power under following circumstances: (Please use TRANSTEK authorized cuff.) CAUTION 1. The battery of LS808-B is built-in rechargeable li-polymer battery, please do not disassemble it by the unauthorized maintenance personel. 2. Under the normal using, it can charge power about 300 times, if the battery cannot charge the power normally or the blood pressure monitor cannot use normally, please connect with the authorized maintenance personel. If measured three times per day, and the battery is fully charged, it can be used for about 20 days. 3. Storge and use the blood pressure monitor at the cool, dry and ventilated environment. Avoid to approach to the fire and the heat source, or it will cause the battery explode. 4. Only can use the Transtek’s authorized AC Adaptor (Model: UE08WCP-060100SPA) to charge the power. You cannot use the blood pressure monitor during the process of charging. 5. During the process of charging, the blood pressure monitor display When the charging is finished, please pull the plug in time. 6. When charging, shall not touch charging connector and the patient simultaneously. BEFORE YOU START BEFORE YOU START Setting the Time,Date and Unit To ensure the stored measurement result has correct time record, please set time and unit before device is used. (3) Press “User 1” button again to confirm [HOUR]. Then the numeral representing [MINUTE] blinks. Before use,switch the button to the “ON” side to turn on the monitor. Note: If the button is on the “OFF” side, there is no reaction when you press any button. (1) When the monitor is off, press and hold User 1 button for 3s to enter Time Setting Mode. (4) Repeat step 2 and 3 to confirm [MINUTE]. (2) As pictured in the right, the blinking numeral representing [HOUR]. Press “Query” button to change the numeral. Each press will increase the numeral by one in a cycling manner. BEFORE YOU START (5) Repeat step 2 and 3 to confirm[MONTH], [DAY] and [YEAR]. BEFORE YOU START (7) After confirming the measurement unit, the LCD will display “dOnE” and the monitor will shut off. (6) Repeat step 2 and 3 to confirm the measurement unit. 10 11 BEFORE YOU START BEFORE YOU START Pair up the Blood Pressure Monitor with Your Device Tie the Cuff (1) Turn on Bluetooth and the app. Make sure both are on when pair-up is proceeding. (2) When the monitor is off, press and hold the User 2 button to start pair-up. The symbol and the symbol will be shown on the LCD alternatively, indicating pair-up is proceeding. If succeed, symbol If fail, symbol will be shown on the LCD. will be shown on the LCD. (3) The monitor will shut off automatically after pair-up process is complete. Bluetooth Module No. : AW8001 Frequency Range 2.402 - 2.480 GHz Supply Voltage 1.8-3.6 V Output Power Range 0 dBm Transmitting Distance 10 meters CAUTION Interference may occur in the vicinity of equipment marked with the following symbol . And LS808-B may interfering vicinity electrical equipment. Keep the monitor at least 20 centimeters away from the human body (especially the head) when the data transmission is proceeding after measurement. To enable the data transmission function, this product should be paired to Bluetooth 1. Remove all accessories from your left arm. If your physician has diagnosed you with poor circulation in your left arm, use your right arm. 2. Roll or push up your sleeve to expose the skin. 3. Apply the cuff to your left arm with your palm facing up. 4. Position the edge of the cuff about 2-3 cm. 5. Fasten the arm cuff around your arm, leaving no extra room between the cuff and your skin. If the cuff is too loose, the measurement will not be accurate. 6. Correct Posture for Patients with Hypertension, especially for Hypertension patient - Bare your arm or wear tights only when starting measurement. - Sit comfortably with legs uncrossed, feet flat on the floor, back and arm supported. The central of the cuff should maintain at the same level as the right atrium of the heart. Resting for 5 minutes before measuring. Wait at least 3 minutes between measurements. This allows your blood circulation to recover. For a meaningful comparison, try to measure under similar conditions. For example, take daily measurements at approximately the same time, on the same arm, or as directed by a physician. end at 2.4 GHz. How to mitigate possible interference? 1. The range between the device and BT end should be reasonably close, from 1 meter to 10 meters. Please ensure no obstacles between the device and BT end so as to obtain quality connection and to lower the RF output range. 2. To avoid interference, other electronic devices (particularly those with wireless transmission / Transmitter) should be kept at least 1 meter away from the monitor. 12 13 MEASUREMENT MEASUREMENT Inflating and measuring. Start Measurement Display and save the results. The data transmission will proceed. When the monitor is off, press User 1 button to turn on the monitor and it will finish the whole measurement, and then save the measure data for User 1. The same to the User 2. (1) When the monitor is off, press the User 1 button to turn on the monitor. LCD display Adjust to zero. (2) Press User 1 button to power off, otherwise it will turn off with one minute. Tips: A. When finish the whole measurement, press another user button, the blood monitor will begin measuring again. B. Maximum 60 records are both for user 1 and user 2. CAUTION 14 1.With LS808-B successfully pair-up with your iPhone, the measurement data will be automatically transmitted to your mobile via Bluetooth. 2.The symbol will disappear after successful data transmission, and you may check your personal health data stored in your iPhone. 3.If the data transmission fails, the symbol will remain. The pending measurement data will be transmitted to your iPhone when next measurement is complete. 15 DATA MANAGEMENT Recall the Records (1) When the monitor is off, press “Query” button to access the memory. DATA MANAGEMENT (4) When in the memory mode, press the User 1 button to recall the measurement history of User 1, or press the User 2 button to recall the measurement history. (2) The LCD will display the latest measuring result of the user ID which completes the last measurement. The record number, measuring date and measuring time will be displayed alternatively. (5) When no history stored for the specific user in the monitor, press “Query” button and the LCD will display as pictured to the right. (3) Press “Query” button to rotate the history records. CAUTION 16 The most recent record (1) is shown first. Each new measurement is assigned to the first (1) record. All other records are pushed back one digit (e.g., 2 becomes 3, and so on), and the last record (60) is dropped from the list. 17 DATA MANAGEMENT Delete the Records DATA MANAGEMENT (3) The LCD will display “dEL dOnE” and then shut off. (1) When under the query mode, press and hold “Query” button for 3 seconds to clear the memory. (2) When the LCD display “dEL ALL”, press “Query” button to confirm. (4) If you wish to stop clearing the memory, you may press the other button, rather than “Query” button to turn off the monitor, or wait until the monitor shuts off. CAUTION 1. 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: too frequent and consecutive multiple measurements; the application of the CUFF and itspressurization on any arm where intravascular access or therapy, or an arterio-venous (A-V) shunt, is present; Inflating the cuff on the arm on the side of a mastectomy. 2. Do not apply the cuff over a wound, otherwise it can cause further injury. 3. 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. 4. Using it in case to result in prolonged impairment of the circulation of the blood of the PATIENT. 5. Don’t kink the connection tube, otherwise, the cuff pressure may continuously increase which can prevent blood flow and result in harmful injury to the PATIENT. 18 19 INFORMATION FOR USER INFORMATION FOR USER Maintenance To obtain the best performance, please follow below instructions. Tips for Measurement It can cause inaccuracy if the measurement is taken in the following circumstances. Within 1 hour after dinner or drinking Within 20 minutes after taking a bath Put in a dry place and avoid the sunshine Avoid immersing it in the water. Clean it with a dry cloth in case. Avoid shaking and collision. Avoid dusty environment and unstable temperature surrounding Use the slightly damp cloth to remove the dirt. Avoid washing the cuff Immediate measurement after tea, coffee, smoking When talking or moving your fingers CAUTION In a very cold environment 20 When you want to discharge urine Please use ACCESSORIES and detachable partes specified/ authorised by MANUFACTURE. Otherwise, it may cause damage to the unit or danger to the user/patients. The device doesn’t need to be calibrated in two years of reliable service. Please dispose of ACCESSORIES, detachable parts, and the ME EQUIPMENT according to the local guidelines. If you have any problems with this device, such as setting up, maintaining or using, please contact with SERVICE PERSONNEL of Transtek. Don’t open or repair the device by yourself. Please report to Transtek if any unexpected operation or events occur. Please use the soft cloth to clean the whole unit. Don’t use any abrasive or volatile cleaners. 21 ABOUT BLOOD PRESSURE ABOUT BLOOD PRESSURE What are systolic pressure and diastolic pressure? When ventricles contract and pump blood out of the heart, the blood pressure reaches its maximum value in the cycle, which is called systolic pressure. When the ventricles relax, the blood pressure reaches its minimum value in the cycle, which is called diastolic pressure. Systolic Diastolic press relax blood entering vein blood discharging artery What is the standard blood pressure classification? The chart on the right is the standard blood pressure classification published by American Heart Association (AHA). AHA Home Guideline for Upper Limit of Normal BP SYS DIA 135 mm Hg 85 mm Hg This chart reflects blood pressure categories defined by American Heart Association. Blood Pressure Category Normal Systolic mmHg (upper#) Diastolic mmHg (lower#) less than 120 and less than 80 Prehypertension 120-139 or 80-89 High Blood Pressure (Hypertension) Stage 1 140-159 or 90-99 160 or higher or 100 or higher Higher than 180 or High Blood Pressure (Hypertension) Stage 2 Hypertensive Crisis (Emergency care needed) Higher than 110 CAUTION Please consult a physician if your measuring result falls outside the range. Kindly note that only a physician could tell whether your blood pressure value has reached a dangerous point. Irregular Heartbeat Detector This Blood Pressure Monitor is equipped with an intelligent function of Irregular Heartbeat (IHB) Detector. During each measurement, this equipment records the heartbeat intervals and works out the standard deviation. If the calculated value is larger than or equal to 15, this equipment will light up the IHB symbol on the screen when displaying the measuring result. CAUTION 22 The appearance of the IHB icon indicates that a pulse irregularity consistent with an irregular heartbeat was detected during measurement. Usually this is NOT a cause for concern. However, if the symbol appears often, we recommend you seek medical advice. Please note that the device does not replace a cardiac examination, but serves to detect pulse irregularities at an early stage. Why does my blood pressure fluctuate throughout the day? 1. Individual blood pressure varies every in one day, it is also affected by the way you tie your cuff and the your measurement position, so please take the measurement at the same condition. 2. The varies of the pressure is greater if the person take medicine. 3. Waiting at least 3 minutes for another measurement. Why the blood pressure I get from the hospital is different from home? The blood pressure is different even during 24 hour because of the weather, emotion, exercise etc, specially the “white coat” in hospital which makes the results are higher than the ones at home. The attention need to pay when you measure your blood pressure at home: If the cuff is tie properly. If the cuff is too tight or too loose. If the cuff is tied on the upper arm. If you feel anxious pressured. You had better take deep breath 2-3 times before beginning. Advice: adjust yourself for 4-5 minutes until you calm down. If the result is the same if measuring on the right arm? It is ok for both arms, but there will be some different results for different arm, so suggest you measure the same arm every time. 23 TROUBLESHOOTING SPECIFICATIONS This 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 here before arranging for servicing. PROBLEM SYMPTOM REMEDY No power Display will not light up. Power is exhausted. Charge the power Low batteries Display is dim or shows Power is low. Charge the power E1 shows E 3 shows E 10 or E 11 shows Error massage E 20 shows E 21 shows EExx,shows on the display. 24 CHECK THIS Communication error Check if the App is on or not,try data transmission again. The cuff is not secure. Refasten the cuff and relax for a moment and then measure again. The monitor detected motion,talking or the pulse is too poor while measuring. Relax for a moment and then measure again. The measurement Loosen the clothing on process does not detect the arm and then the pulse signal. measure again. The treatment of the measurement failed. A calibration error occurred. Relax for a moment and then measure again. Retake the measurement. If the problem persists, contact the retailer or our customer service department for further assistance.Refer to the warranty for contact information and return instructions. Power supply Display moder Measurement mode Measurement range Accuracy Normal working condition Storage & transportation condition Measurement perimeter of the upper arm Net Weight External dimensions Attachment Mode of operation Degree of protection 3.7V 1000mAH Built-in rechargeable li-polymer battery, 6V 1A AC Adaptor Blue LCD with White Backlight V.A.= 86.1mm(L) x24mm(W) Oscillographic testing mode Rated cuff pressure: 0kPa-40kPa (0mmHg-300mmHg) Measurement pressure: 5.3kPa-30.7kPa (40mmHg-230mmHg) pulse value:(40-199)beat/minute Pressure: 5℃-40℃within±0.4kPa(3mmHg) pulse value:±5% Temperature:5℃ to 40℃ Relative humidity: ≤85%RH Atmospheric pressure: 86kPa to 106kPa Temperature:-20℃ to 60℃ Relative humidity: 10%RH to 93%RH Atmospheric pressure: 50kPa to 106kPa About 22cm-42cm Approx.265 g Approx.130.9mm×73mm×29.4mm AC Adaptor,user manual Continuous operation Type BF applied part Protection against ingress of water IP22, It means the device could protected against solid foreign objects of 12.5 mm and greater, and against vertically falling water drops when ENCLOSURE tilted up to 15° Software version V01 Device classification Battery Powered Mode: Internally Powered ME Equipment AC Adaptor charged Mode: Class II ME Equipment WARNING: No modification of this equipment is allowed. 25 COMPLIED STANDARDS LIST ATHORIZED COMPONENT Athorized Component Please use the TRANSTEK authorized adaptor Complied Standards List Risk management ISO/EN 14971:2012 Medical devices — Application of risk management to medical devices Labeling ISO/EN 15223-1:2012 Medical devices. Symbols to be used with medical device labels, labelling and information to be supplied. General requirements User manual EN 1041: 2008 Medical equipment manufacturers to provide information General Requirements for Safety Adaptor Type: UE08WCP-060100SPA Input: 100-240V 50-60Hz,400mA 1A Output: 6V (Conforms to UL Certification) Contact Information For more information about our products, please visit www.transtek.cn.you can get customer service, usual problems and customer download, transtek will serve you anytime. Manufactured by: GUANGDONG TRANSTEK MEDICAL ELECTRONICS CO., LTD Company: GUANGDONG TRANSTEK MEDICAL ELECTRONICS CO., LTD Address: Zone A, 5/F., Investment Building , No. 12, Huizhan East Rd., Torch Development District, Zhongshan, Guangdong, 528437, China 26 IEC 60601-1: 2005+A1：2012 Medical electrical equipment - Part 1: General requirements for basic safety and essential performance Electromagnetic compatibility IIEC/EN 60601-1-2:2007 Medical electrical equipment Part 1-2: General requirements for basic safety and essential performance - Collateral standard:Electromagnetic compatibility - Requirements and tests Performance requirements IEC 80601-2-30:2009 Medical electrical equipment- Part 2-30: Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers Clinical investigation Software life-cycle processes ISO 81060-2:2009 Non-invasive sphygmomanometers Part 2 : Clinical validation of automated measurement type IEC/EN 62304:2006+AC: 2008 Medical device software - Software life cycle processes 27 FCC STATEMENT EMC GUIDANCE 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. Caution: The user is cautioned that changes or modifications not expressly approved by the party responsible for compliance could void the user's authority to operate the equipment. NOTE: This equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to Part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential installation. This equipment generates, uses and can radiate radio frequency energy and, if not installed and used in accordance with the instructions, may cause harmful interference to radio communications. However, there is no guarantee that interference will not occur in a particular installation. If this equipment does cause harmful interference to radio or television reception, which can be determined by turning the equipment off and on, the user is encouraged to try to correct the interference by one or more of the following measures: -- Reorient or relocate the receiving antenna. -- Increase the separation between the equipment and receiver. -- Connect the equipment into an outlet on a circuit different from that to which the receiver is connected. -- Consult the dealer or an experienced radio/TV technician for help. EMC Guidance 1. The Blood Pressure Monitor needs special precautions regarding EMC and needs to be installed and put into service according to the EMC information provided in the ACCOMPANYING DOCUMENTS 2. Wireless communications equipment such as wireless home network devices, mobile phones, cordless telephones and their base stations, walkie-talkies can affect this equipment and should be kept at least a distance d = 3,3 m away from the equipment. (Note. As indicated in Table 6 of IEC 60601-1-2:2007 for ME EQUIPMENT, a typical cell phone with a maximum output power of 2 W yields d = 3,3 m at an IMMUNITY LEVEL of 3 V/m) FCC Radiation Exposure Statement: This equipment complies with FCC radiation exposure limits set forth for an uncontrolled environment. This transmitter must not be co-located or operating in conjunction with any other antenna or transmitter. 28 29
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xmp.iid:C369CFF3216ADF11B466D7F75EC58098, xmp.iid:C469CFF3216ADF11B466D7F75EC58098, xmp.iid:C569CFF3216ADF11B466D7F75EC58098, xmp.iid:504E54E31E6EDF11A2BDADDD17472490, xmp.iid:C56D130EBE9ADF11A952BC6F8ABEB51F, xmp.iid:A3AE97C021C4E11186D98A42EEB52AC4, xmp.iid:17A4E7CF652DE2119855D8860B2BB0F4, xmp.iid:037252FD4235E211A1F4B1D563F6A695, xmp.iid:454E5A9DD740E2119E19F84E85DA2D77, xmp.iid:F9A00446BF5AE211970AF988274C84C1, xmp.iid:77018A920EA0E211A5D6878EE5BD1F95 History When : 2008:04:17 14:19:15+05:30, 2008:05:15 16:23:06-07:00, 2008:05:15 17:10:45-07:00, 2008:05:15 22:53:33-07:00, 2008:05:15 23:07:07-07:00, 2008:05:16 10:35:43-07:00, 2008:05:16 10:40:59-07:00, 2008:05:16 11:26:55-07:00, 2008:05:16 11:29:01-07:00, 2008:05:16 11:29:20-07:00, 2008:05:16 11:30:54-07:00, 2008:05:16 11:31:22-07:00, 2008:05:16 12:23:46-07:00, 2008:05:16 13:27:54-07:00, 2008:05:16 13:46:13-07:00, 2008:05:16 15:47:57-07:00, 2008:05:16 15:51:06-07:00, 2008:05:16 15:52:22-07:00, 2008:05:22 13:28:01-07:00, 2008:05:22 16:23:53-07:00, 2008:05:28 16:45:26-07:00, 2008:06:02 13:25:25-07:00, 2008:06:09 14:58:36-07:00, 2008:06:11 14:31:27-07:00, 2008:06:11 22:37:35-07:00, 2008:06:18 22:24:01+07:00, 2008:06:19 20:30:34-07:00, 2008:06:24 14:13:53+08:00, 2008:06:24 15:23:44+08:00, 2008:06:26 06:03:48-07:00, 2008:07:02 13:54:27-07:00, 2008:07:21 16:58:31+05:30, 2008:09:05 03:21:29-07:00, 2008:09:05 04:21:56-07:00, 2010:04:29 15:41:12+08:00, 2010:05:27 17:32:24+08:00, 2010:05:28 16:18:49+08:00, 2010:05:28 16:46:46+08:00, 2010:05:28 16:47:33+08:00, 2010:06:02 17:05:13+08:00, 2010:07:29 11:04:51+08:00, 2012:07:02 16:49:24+08:00, 2012:11:13 15:43:27+08:00, 2012:11:23 15:54:20+08:00, 2012:12:08 09:44:07+08:00, 2013:01:10 08:47:13+08:00, 2013:04:08 13:42:50+08:00 History Software Agent : Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS4, Adobe Illustrator CS5, Adobe Illustrator CS5, Adobe Illustrator CS5, Adobe Illustrator CS5, Adobe Illustrator CS5, Adobe Illustrator CS5 History Changed : /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, /, / History Params : from application/vnd.adobe.illustrator to application/vnd.adobe.illustrator Startup Profile : Print Has Visible Overprint : True Has Visible Transparency : True N Pages : 1 Max Page Size W : 201.598375 Max Page Size H : 138.759489 Max Page Size Unit : Millimeters Font Name : Arial-BoldMT, ArialMT, Calibri, TimesNewRomanPSMT, AdobeSongStd-Light, SimSun, SimHei Font Family : Arial, Arial, Calibri, Times New Roman, Adobe 宋体 Std, 宋体, 黑体 Font Face : Bold, Regular, Regular, Regular, L, Regular, Regular Font Type : Open Type, Open Type, Open Type, Open Type, Open Type, TrueType, TrueType Font Version : Version 3.00, Version 3.00, Version 1.02, Version 3.00, Version 5.002;PS 5.002;hotconv 1.0.49;makeotf.lib2.0.15106, Version 3.12, Version 3.02 Font Composite : False, False, False, False, False, False, False Font File Name : ARIALBD.TTF, ARIAL.TTF, CALIBRI.TTF, TIMES.TTF, AdobeSongStd-Light.otf, simsun.ttc, simhei.ttf Plate Names : Cyan, Magenta, Yellow, Black, Deep Black, PANTONE Reflex Blue C, PANTONE 286 CVU Swatch Groups Group Name : 默认色板组 Swatch Groups Group Type : 0 Swatch Groups Colorants Swatch Name: AutoCAD Color 3 Swatch Groups Colorants Type : PROCESS Swatch Groups Colorants Tint : 100.000000 Swatch Groups Colorants Mode : CMYK Swatch Groups Colorants Cyan : 92.971700 Swatch Groups Colorants Magenta : 87.972802 Swatch Groups Colorants Yellow : 89.019603 Swatch Groups Colorants Black : 79.998499 Producer : Adobe PDF library 9.90 Page Count : 16 Creator : Adobe Illustrator CS5EXIF Metadata provided by EXIF.tools