Transtek Medical Electronics TMB1591-B Blood Pressure Monitor, Automated Blood Pressure System User Manual
Guangdong Transtek Medical Electronics Co.,Ltd Blood Pressure Monitor, Automated Blood Pressure System
User Manual
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| Document ID | 2877849 |
| Application ID | MBplendd8vjF8y7G8jvk5Q== |
| Document Description | User Manual |
| Short Term Confidential | No |
| Permanent Confidential | No |
| Supercede | No |
| Document Type | User Manual |
| Display Format | Adobe Acrobat PDF - pdf |
| Filesize | 375.88kB (4698449 bits) |
| Date Submitted | 2016-01-19 00:00:00 |
| Date Available | 2016-01-20 00:00:00 |
| Creation Date | 2015-06-02 13:50:31 |
| Producing Software | Adobe PDF library 9.90 |
| Document Lastmod | 2015-09-07 18:50:00 |
| Document Title | User Manual |
| Document Creator | Adobe Illustrator CS5 |
| Document Author: | Shuting |
version:1.0 User Manual Blood Pressure Monitor TMB-1591 Arm Type Thank you very much for selecting TRANSTEK Blood Pressure Monitor TMB-1591. Guangdong Transtek Medical Electronics Co., Ltd. Zone A, No.105 ,Dongli Road, Torch Development District, Zhongshan,528437,Guangdong,China To use the monitor correctly and safely, please read the manual thoroughly. Please keep this manual well in order to reference in future. CATALOGUE CATALOGUE Table of Contents INTRODUCTION........................................................................................2 General Description Safety Information Indications for Use LCD Display Signal Monitor Components BEFORE YOU START................................................................................7 The Choice of Power Supply Installing and Replacing the Batteries MEASUREMENT.......................................................................................8 Pairing Tie the Cuff Start the Measurement INFORMATION FOR USER......................................................................13 Tips for measurement Maintenances ABOUT BLOOD PRESSURE....................................................................15 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 the hospital? Is the result the same if measuring on the right arm? TROUBLESHOOTING..............................................................................17 SPECIFICATIONS.....................................................................................18 AUTHORIZED COMPONENT ..................................................................19 CONTACT INFORMATION........................................................................19 COMPLIED STANDARDS LIST.................................................................20 FCC STATEMENT......................................................................................21 IC STATEMENT..........................................................................................22 EMC GUIDANCE.......................................................................................23 INTRODUCTION General Description Thank you for selecting TRANSTEK arm type blood pressure monitor (TMB-1591). The monitor features blood pressure measurement, pulse rate measurement and the result storage. The design provides you with two years of reliable service. Readings taken by the TMB-1591 are equivalent to those obtained by a trained observer using the cuff and stethoscope auscultation 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: 68mm*90mm Digital LCD display with White backlight Maximum 99 records Measuring during inflation technology Indications for Use The Transtek Blood Pressure Monitor is digital monitors intended for use in measuring blood pressure and heartbeat rate with arm circumference ranging from 22cm to 42cm(about 8¾˝-16½˝). It is intended for adult indoor use only. Measurement Principle This product uses the Oscillometric Measuring method to detect blood pressure. Before every measurement, the unit establishes a “zero pressure” equivalent to the air pressure. Then it starts inflating the arm cuff, meanwhile, the unit detects pressure oscillations generated by beat-to-beat pulsatile, which is used to determine the systolic and diastolic pressure, and also pulse rate. The device also compares the longest and the shortest time intervals of detected pulse waves to mean time interval then calculates standard deviation. The device will display a warning signal with the reading to indicate the detection of irregular heartbeat when the difference of the time intervals is over 25%. INTRODUCTION Safety Information The signs below might be in the user manual, labeling or other component. They are the requirement of standard and using. F1 Symbol for “THE OPERATION GUIDE MUST BE READ” Symbol for “TYPE BF APPLIED PARTS” The Bluetooth Combination Mark Symbol for “ENVIRONMENT PROTECTION – Electrical waste products should not be disposed of with household waste. Please followlocal guidelines.” Symbol for “MANUFACTURER” Symbol for “DIRECT CURRENT” For indoor use only Symbol for “Class II Equipment” WARNING:These warning notes must be observed to preventany injury to the user. IP22 Caution: These notes must be observed to prevent any damage to the device. T1A/250V Φ3.6*10CCC SN Symbol for “SERIAL NUMBER” The ingress protection: the device could protected against solid foreign objects of 12.5mm and greater, and against vertically falling water drops when ENCLOSURE tilted up to 15° Symbol for “KEEP DRY” WARNING 1. The device is not suitable for measuring the blood pressure of children. Ask your doctor before using it on older children. 2. The device is not suitable for use on pregnant women, patients with implanted, electrocical devices, patients with pre-elcampsia, 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 3.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. 4.Please keep the unit out of reach of infants, children or pets, since inhalation or swallowing of small parts is dangerous or even fata. 5. Do not dispose of batteries in fire. Batteries may explode or leak. INTRODUCTION CAUTION This device is intended only for adult use in homes. This device is intended for non-invasive measuring and monitoring of arterial blood pressure. It is not intended for use on extremities other than arm or for functions other than obtaining a blood pressure measurement. 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. 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. Too frequent and consecutive measurements could cause disturbances in blood circulation and injuries. Do not wrap the cuff on the same arm which other monitoring ME EQUIPMENT is applied simultaneously, because this could cause temporary loss of function of those simultaneously-used monitoring ME EQUIPMENT. 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. 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. This unit is not suitable for continuous monitoring during medical emergencies or operations. This device cannot be used with HF surgical equipment at the same time. This device is not intended for patient transports outside a healthcare facility. To avoid measurement errors, please avoid the condition of strong electromagnetic field radiated interference signal or electrical fast transient/burst signal. The operator shall not touch output of batteries/adapter and the patient simultaneously. Manufacturer will make available on request circuit diagrams, component parts list etc. 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.Never apply the cuff over hurt skin. Do not use the unit in case of existing polyester resp. synthetic allergies. Be careful to strangulation due to cables and hoses, particularly due to excessive length. Do not connect the air hose to other medical equipment, as this could cause air to be pumped into intravascular systems or high pressure, what could lead to dangerous injuries. Before use, make sure the device functions safely and is in proper working condition. 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. Please use ACCESSORIES and detachable partes specified/ authorised by MANUFACTURE. Otherwise, it may cause damage to the unit or danger to the user/patients. Please dispose of ACCESSORIES, detachable parts, and the ME EQUIPMENT according to the local guidelines. Please do not attempt to repair the unit yourself in the event of malfunctions. Only have repairs carried out by authorized service centers. Please report to Manufacturer if any unexpected operation or events occur. The device doesn’t need to be calibrated in two years of reliable service. Please use the soft cloth to clean the whole unit. Don’t use any abrasive or volatile cleaners. The patient is an intended operator.The patient can measure and change battery under normal circumstances and maintain the device and its accessories according to the user manual. Don't press or restrict the connection tubing during measurement. The device is not intended for public use. INTRODUCTION LCD Display Signal SYS mmHg DIA mmHg PULSE /MIN SYMBOL DESCRIPTION EXPLANATION Systolic blood pressure High pressure result Diastolic blood pressure Low pressure result Pulse Pulse/minute mmHg Measurement Unit of the blood pressure Irregular heartbeat Irregular heartbeat detection Battery Indicator Indicate the current battery Grade The grade of the blood pressure Shocking reminder Shocking will result in inaccurate Data transmission error Data transmission error Heartbeat Heartbeat dectetion during measurement INTRODUCTION BEFORE YOU START The Choice of Power Supply Monitor Components 1.Battery powered mode: CUFF 6VDC 4*AA alkaline batteries (Notes: A groups of new batteries can be used about 750 times. AIR HOSE 2.AC adaptor powered mode: 6V 1A (Can be supplied by AC adaptor model UE08WCP-060100SPA !) AIR CONNECTOR PLUG Right picture is the hole in for power adaptor. LCD DISPLAY CAUTION In order to get the best effect and protect your monitor,please use the right battery and special power adaptor. The power adapter is a part of the device. ON/STANDBY BUTTON After using, please pull out the adaptor plug insulates from the main supply. Do not position the device in a position where it is difficult to disconnect from Component list of pressure measuring system 1 Cuff 2 Air pipe 3 PCBA 4 Pump 5 Valve DC POWER SOCKET the supply mains. Installing and Replacing the Batteries BATTERY COMPARTMENT List 1. Blood Pressure Monitor 2. Cuff (22cm~42cm) (TMB-1591) (Type BF applied part) １.Slide off the battery cover. ２.Install the batteries by matching the correct polarity, as shown. ３.Replace the cover. Replace the batteries whenever the below happen The shows The display dims The display does not light up 3. 4*AA alkaline Batteries 4. User manual CAUTION Remove batteries if the device is not likely to be used for some time. The old batteries are harmful to the environment, do not dispose with other daily trash. 5. AC adaptor (UE08WCP-060100SPA) Remove the old batteries from the device and follow your local recycling guidelines. MEASUREMENT MEASUREMENT Pairing Turn on Bluetooth and APP. Make sure both are ON when pairing is proceeding. When the blood pressure monitor is off, press On/Standby button for 2 full seconds to enter bluetooth pairing mode. The symbol flashes, indicating the pairing is proceeding. Tie the Cuff 1.Tie the cuff on your upper arm, then position the tube off-center toward the inner side of arm in line with the little finger. 2.The cuff should be snug but not too tight. You should be able to insert one finger between the cuff and your arm. 3.Sit comfortably with your arm resting on a flat surface. Then please select the user ID you want to connect with your smartphone on the app to continute the pair-up. If succeed, symbol will turn off. If fail, symbol turns off. 2~3cm will be shown. Then blood pressure monitor will flash all the time until the blood pressure Bluetooth Module No.: AW2540MV1 RF Frequency Range: 2402 MHz to 2480 MHz Output Power Range: -1 dBm Supply Voltage: 2V-3.6 V Transmitting Distance: 10 meters 4.Correct position: - 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 center of the cuff should be at the same level as the right atrium of the heart. Rest 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 upper arm, or as directed by a physician. MEASUREMENT MEASUREMENT Start Measurement When the blood pressure monitor is off, press On/Standby button to turn it on, it will finish the whole measurement. LCD display Inflating and Measuring The blood pressure monitor will proceed to data transmission after measurement. The bluetooth symbol flashes on the LCD indicates data is transmitting. Adjust to zero. Display and save the result. After successful transfer, the device powers off the Bluetooth radio and the icon (and rectangle) are removed. If the user presses and releases the On/Standby button, another reading is initiated. If the user presses and holds the On/Standby button for 2 seconds, the device powers down. Or if there is no operation, after a 10 seconds of inactivity, the device powers down. Notes: During inflation, the heart icon in the upper left blinks in accordance with the user’s pulse rate. Additionally, during inflation the progress metre to the right of the digits builds vertically up as the pressure increases according to the table below. Segments 10 Pressure Segments Pressure >= 0 >= 140 >= 40 >= 160 >= 80 >= 180 >= 120 >= 200 11 MEASUREMENT INFORMATION FOR USER Tips for Measurement During the measurement, if you press the On/Standby button to stop the measurement, the numerics are cleared. It will display as below: Measurements may be inaccurate if taken in the following circumstances. wait at least 1 hour after dinner or drinking If you press and release the On/Standby button, another reading is initiated. If you press and hold the On/Standby button for 2 seconds, the device powers down. Or if there is no operation, after a 10 seconds of inactivity, the device powers down. Immediate measurement after tea, coffee, smoking Wait at least 20 minutes after taking a bath When talking or moving your fingers In a very cold environment When you want to discharge urine CAUTION 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 oldest record (99) is dropped from the list. 12 13 INFORMATION FOR USER ABOUT BLOOD PRESSURE What are systolic pressure and diastolic pressure? Maintenance In order to get the best performance, please follow the instructions below. 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? Put in a dry place and avoid the sunshine Avoid touching water, clean it with a dry cloth in case. 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 135 mm Hg DIA 85 mm Hg Avoid intense shaking and collisions Avoid dusty and unstable temperature environment This chart reflects blood pressure categories defined by American Heart Association. Blood Pressure Category Systolic mmHg (upper#) Diastolic mmHg (lower#) less than 80 80-89 less than 120 and Prehypertension 120-139 or High Blood Pressure (Hypertension) Stage 1 140-159 or 90-99 160 or higher or 100 or higher Higher than 180 or Normal High Blood Pressure (Hypertension) Stage 2 Hypertensive Crisis (Emergency care needed) Higher than 110 CAUTION Only a physician can tell your normal BP range. Please contact a physician if your measuring result falls out of the range. Please note that only a physician can tell whether your blood pressure value has reached a dangerous point. Irregular Heartbeat Detector Using wet cloths to remove dirt Avoid washing the cuff An irregular heartbeat is detected when a heartbeat rhythm varies while the unit is measuring the systolic and diastolic blood pressure.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,the irregular heartbeat symbol appears on the symbol when the measurement results are displayed. CAUTION 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. 14 15 ABOUT BLOOD PRESSURE TROUBLESHOOTING 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. Why does my blood pressure fluctuate throughout the day? 1. Individual blood pressure varies multiple times everyday. It is also affected by the way you tie your cuff and your measurement position, so please take the measurement under the same conditions. PROBLEM SYMPTOM No power 2.If the person takes medicine, the pressure will vary more. 3.Wait at least 3 minutes for another measurement. Why do I get a different blood pressure at home compared to the hospital? The blood pressure is different even throughout the day due to weather, emotion, exercise etc, Also, there is the “white coat” effect, which means blood pressure usually increases in clinical settings. Is the result the same if measuring on the right arm? It is ok for both arms, but there will be some different results for different people. We suggest you measure the same 16 arm every time. Low batteries What you need to pay attention to when you measure your blood pressure at home: If the cuff is tied properly. If the cuff is too tight or too loose. If the cuff is tied on the upper arm. If you feel anxious. Taking 2-3 deep breaths before beginning will be better for measuring. Advice: Relax yourself for 4-5 minutes until you calm down. Error massage Display will not light up. CHECK THIS REMEDY Batteries are exhausted. Replace with new batteries Batteries are inserted incorrectly. Insert the batteries correctly AC adaptor is inserted incorrectly. Insert the AC adaptor tightly The display indicates the Batteries are low. “BAT LO” message, pauses for 3 seconds. The battery icon shows empty (does not flash.) Replace with new batteries Unsuccessful pairing. Check if both the APP and Bluetooth are on, operate and send the data again. E 01 shows The cuff is not secure. Readjust the cuff and relax for a moment and then measure again. E 02 shows The cuff is too tight or the inflation is too fast. Refasten the cuff and then measure again. The pressure of the cuff is excess. The monitor detected motion,talking or the pluse is too poor while measuring. Refasten the cuff and then measure again. shows E 03 shows E 10 or E 11 shows Movement can affect the measurement.Relax for a moment and then measure again. E 20 shows The measurement Loosen the clothing on process does not detect the arm and then the pulse signal. measure again. E 21 shows Measure incorrectly. EExx,shows on the display. 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. 17 SPECIFICATIONS Power supply AUTHORIZED COMPONENT Battery powered mode: 6VDC 4*AA alkaline batteries AC adaptor powered mode: 6V 1A (Can be supplied by AC adaptor model UE08WCP-060100SPA !) Display mode Authorized Component １.please use the TRANSTEK authorized adapter. Digital LCD V.A.68mm*90mm Measurement mode Oscillographic testing mode Measurement range Rated cuff pressure: 0mmHg-300mmHg Measurement pressure: SYS:60mmHg-230mmHg DIA: 40mmHg-130mmHg pulse value:(40-199)beat/minute Accuracy Pressure: 5℃-40℃ within±3mmHg pulse value:±5% Normal working condition Storage & transportation condition Measurement perimeter of the upper arm Net Weight External dimensions Attachment Temperature:-20℃to 60℃ Relative Humidity: 10%RH to 93%RH Atmospheric Pressure: 50kPa to 106 kPa About 22cm~42cm Approx.300g(Excluding the dry cells) Approx.92mm*140mm*46mm 4*AA alkaline batteries,user manual Mode of operation Continuous operation Degree of protection Type BF applied part Protection against ingress of water Software Version 18 Temperature:5℃ to 40℃ Relative humidity ≤85%RH Atmospheric pressure: 86kPa to 106kPa Adapter Type： UE08WCP-060100SPA Input：100~240V，50~60Hz,400mA Output：6V 1A ( Conforms to UL certificate ) 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, No.105 ,Dongli Road, Torch Development District, Zhongshan,528437,Guangdong,China IP20 V01 WARNING: No modification of this equipment is allowed. 19 COMPLIED STANDARDS LIST Complied Standards List Risk management 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 IEC 60601-1: 2005+A1：2012 Medical electrical equipment - Part 1: General requirements for basic safety and essential performance IEC 60601-1-11 Medical electrical equipment - Part 1-11: General requirements for basic safety and essential performance - Collateral standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment IEC60601-1-11:2010 Electromagnetic compatibility IEC/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 and Clinical investigation IEC 80601-2-30:2009+A1:2013 Medical electrical equipment- Part 2-30: Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers ISO81060-2 Non-invasive sphygmomanometers — Part 2: Clinical validation of automated measurement type Software life-cycle processes Usability 20 ISO/EN 14971:2012 Medical devices — Application of risk management to medical devices IEC/EN 62304:2006+AC: 2008 Medical device software - Software life cycle processes IEC 62366 Medical devices - Application of usability engineering to medical devices (IEC 62366:2007) IEC 62366:2007+A1:2014 IEC 60601-1-6:2010+A1:2013 Medical electrical equipment - Part 1 -6 : General requirements for basic safety and essential performance - collateral standard : Usability FCC STATEMENT FCC Statement FCC ID: OU9TMB1591-B 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. 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. 21 IC STATEMENT IC Statement IC ID：12725A-TMB1591B This device complies with Industry Canada license-exempt RSS standard(s). Operation is subject to the following two conditions: (1) this device may not cause interference, and (2) this device must accept any interference, including interference that may cause undesired operation of the device. Le présent appareil est conforme aux CNR d'Industrie Canada applicables aux appareils radio exempts de licence. L'exploitation est autorisée aux deux conditions suivantes : (1) l'appareil ne doit pas produire de brouillage, et (2) l'utilisateur de l'appareil doit accepter tout brouillage radioélectrique subi, même si le brouillage est susceptible d'en compromettre le fonctionnement. 22 EMC GUIDANCE EMC Guidance 1) This equipment needs to be installed and put into service in accordance with the information provided in the user manual; 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=3,3m 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, 3m at an IMMUNITY LEVEL of 3V/m) 23
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2010:11:08 09:13:48+08:00, 2010:11:09 11:24:26+08:00, 2011:01:13 11:20:28+08:00, 2011:01:14 09:32:45+08:00, 2012:12:08 13:29:51+08:00, 2012:12:21 08:57:37+08:00, 2012:12:29 16:12:58+08:00, 2012:12:29 17:15:49+08:00, 2013:01:02 09:32:35+08:00, 2013:01:02 09:35:24+08:00, 2015:06:02 13:50:26+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 CS5, 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 Derived From Instance ID : uuid:72d05f54-5877-4a1b-b4a6-329347296569 Derived From Document ID : xmp.did:475A56547754E2118865C2E3DC882209 Derived From Original Document ID: uuid:9E3E5C9A8C81DB118734DB58FDDE4BA7 Derived From Rendition Class : proof:pdf Startup Profile : Basic RGB N Pages : 1 Has Visible Transparency : True Has Visible Overprint : True Max Page Size W : 160.000053 Max Page Size H : 139.999896 Max Page Size Unit : Millimeters Font Name : ArialRoundedMTBold, Arial-BoldMT, ArialMT, Arial-Black, TimesNewRomanPSMT, Tahoma, FZDHTJW--GB1-0, AdobeSongStd-Light, SimSun, SimHei, HelveticaNeue-Bold, HelveticaNeue Font Family : Arial Rounded MT Bold, Arial, Arial, Arial, Times New Roman, Tahoma, 方正大黑简体, Adobe 宋体 Std, 宋体, 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Swatch Groups Group Name : 初始屏幕 Swatch Groups Group Type : 1 Swatch Groups Colorants Swatch Name: R=180 G=58 B=228 Swatch Groups Colorants Mode : CMYK Swatch Groups Colorants Type : PROCESS Swatch Groups Colorants Cyan : 48.046899 Swatch Groups Colorants Magenta : 78.906298 Swatch Groups Colorants Yellow : 0.000000 Swatch Groups Colorants Black : 0.000000 Producer : Adobe PDF library 9.90 Keywords : GBF-1251-B Page Count : 13 Author : Shuting Subject : User ManualEXIF Metadata provided by EXIF.tools