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全彩Digital Laptop Diagnostic Ultrasound Equipment

作者:高考题库网
来源:https://www.bjmy2z.cn/gaokao
2021-01-28 07:31
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全彩-finisher

2021年1月28日发(作者:后退英文)








Digital Laptop Diagnostic Ultrasound Equipment



Operation Manual




(


Model: XK/21355 LCD


)











For your kind attention


Dear customer,


Thank you for choosing xukang product.


It’s


our


great


honor


that


you’ve


chosen


xukang


product.


In


order


that


you


can


get


general


and


concrete


information


on


operation,


installation and trouble-


shooting of our product, we’ve released this manual. It is strongly recommended that you peruse this manual prior


to operating of the product in case there is any damage or loss caused by mis-operation which the company will not be responsible for.


We’ve tried our best to avoid any man


-


made mistake before releasing of this manual. However we’d beg your pardon if there is


any mistake in the content of the manual or faults during printing, assembling or recycling.


We may make some minor adjustments to the hardware or software of our product to improve its performance and reliability.


Maybe there are some discrepancies between descriptions in this manual and the product


you receive. This won’t effect your


operating of the product. Please be kindly noted.



In order that you can get our full-round after-sale service, please register your product as soon as possible.



How to register:


1.


2.


Visit our website at:





Click Customer Service Centre, and fill in requested information


Or fill in our Product Registration card and mail it to our Customer Service Centre. Mail address can be found in the Product


Registration card.


Or fill in our Product Registration card and fax it to +86-28-87652638, extension to our Customer Service Centre.


3.


If you have any difficulty or query in operating our operate, please call our service No: +86-28-87652968


Thank you for your kind cooperation.





























Sichuan Xukang Medical Electrical Appliances Co., Ltd.











EC Declaration of Conformity


Manufacturer: Sichuan Xukang Medical Electrical Appliances Co., Ltd.


Add.: No.58 HeGang Road south Zone, ChengDu Modern Industrial Haven Chengdu, China


European Representative: Wellkang Ltd t/a Wellkang Tech Consulting



Add.: Suite B, 29 Harley Street LONDON W1G 9QR England, United Kingdom


Classification (MDD, Annex IX): IIa (According to MDD, Rule 10)



We herewith declare that the above mentioned products meet the provisions of the following EC Council Directives and Standards. All


supporting documentations are retained under the premises of the manufacturer.





DIRECTIVES


General Applicable Directives:


Medical Device Directive: COUNCIL DIRECTIVE 93/42/EEC concerning medical devices (MDD 93/42/EEC).


Standards: ISO 1000:1992+A1:1998, ISO13485:2003, EN ISO14971: 2007, EN 980:2008, EN 60601-1-4: 1999


IEC 60601-1:1988+A1:1991+A2:1995, IEC 60601-1-2:2007, EN 1041: 1998, IEC/TR 60878: 2003,



IEC 60601-2-25:1993+A1 :1999, EN ISO780: 1999, EN 60417-1:2002.


Identification number





















































Manufacturer’s statement



Copyright


Copyright


?


Sichuan Xukang Medical Electrical Appliances Co., Ltd.2011.


Sichuan Xukang Medical Electrical Appliances Co., Ltd. (hereinafter short as Xukang) makes no warranty of any kind with regard to this


material, including, but not limited to the implied warranties of merchantability and fitness for a particular purpose.


Xukang assumes no


responsibility for any errors that may appear in this document, or for incidental or consequential damage in connection with the furnishing,


performance or use of this material.


No part of this document can be photocopied, reproduced or translated to another language without prior written consent of Xukang .


Xukang will make continuous improvement in features and functions for future publication of new equipment without prior notice. We beg


your pardon for the inconvenience, if any.


Version


Version: Laptop


P/N No.:




Release date:



EC-Representative


Wellkang Ltd t/a Wellkang Tech Consulting













































Add.: Suite B, 29 Harley Street LONDON W1G 9QR England, United Kingdom
































Responsibility of the manufacturer


Xukang only considers itself responsible for any effects on safety, reliability and performance of the equipment if:


Assembly


operations,


extensions,


re-adjustments,


modifications


or


repairs


are


carried


out


by


personnel


authorized


by


us,


and


the


electrical installation of the relevant room complies with safety standards.


NOTE


:


This device is not intended for home use.


:



This device is not intended for treatment.


WARNING


Label guide


WARNING



A


WARNING


label advises against certain actions or situations that could result in personal injury or death.


NOTE



A


NOTE



label


advises


against


certain


actions


or


situations


that


could


damage


equipment,


produce


inaccurate


data,


or


invalidate


a


procedure.




























































































Content


CHAPTER 1 OVERVIEW



................... .................................................. .................................................. ...................................


3



1.1



C


HARACTERISTIC


.. .................................................. .................................................. .................................................. ..................... 3



1.2



C


LASSIFICATIONS


. .................................................. .................................................. .................................................. ...................... 3



1.3



C


OMPONENTS OF STRUCTURE



.................. .................................................. .................................................. ..................................... 3



1.4



O


PERATION FUNCTIONS OF


E


QUIPMENT


....... .................................................. .................................................. .................................. 3



1.5



S


COPE OF


A


PPLICATION


< p>
............................................ .................................................. .................................................. .................... 4



1.6



C


ONTRAINDICATION


.................................................. .................................................. .................................................. .................... 4



1.7



S


TANDARD


< br>............................................... .................................................. .................................................. .................................... 4



1.8



C


OMMITMENT TO PRODUCTS




SAFETY


..................... .................................................. .................................................. .................... 4



CHAPTER 2 SYSTEM INTRODUCTION



.


... .................................................. .................................................. .............................


5



2.1



T


ECHNICAL


S


PECIFICATION



.


.............................. .................................................. .................................................. ............................. 5



2.2



F


UNCTION REQUIREMENTS AND FREQUENCY CONVERSION POINTS OF OPTIONAL PROBES



.


......... .................................................. ........... 5



2.3



P


OWER



.


...................................... .................................................. .................................................. ................................................. 5



2.5



U


LTRASOUND OUTPUT POWER


(


IN THE APPENDIX


1)


.


............. .................................................. .................................................. ........... 6



2.6



O


PTIONAL CONFIGURATION



.


.. .................................................. .................................................. .................................................. ....... 6



2.7



S


AFETY


.......... .................................................. .................................................. .................................................. ........................... 6



2.8



E


NVIRONMENTAL ADAPTATION



.


..... .................................................. .................................................. .................................................. 6



2.9



B


ASIC


C


IRCUIT


D


IAGRAM


.


.................................... .................................................. .................................................. .......................... 6



2.10



B


ASIC


P


RINCIPLE



.


.................................. .................................................. .................................................. ..................................... 6



CHAPTER 3 EQUIPMENT INSTALLATION


.......................... .................................................. .................................................. ...


7



3.1



R


EQUIREMENT ON


E


NVIRONMENT


< p>
............................................ .................................................. .................................................. ...... 7



3.2



R


EQUESTS OF APPEARANCE



................. .................................................. .................................................. ......................................... 7



3.3



C


HECK


-


UP AFTER UNPACKING CARTON


...................... .................................................. .................................................. ..................... 7



3.4



I


NSTALLATION



........................................... .................................................. .................................................. .................................... 7



3.5



G


ROUNDING


P


ROTECTION



.


................................. .................................................. .................................................. ........................... 9



CHAPTER 4 CHECK & MAINTENANCE



.


.... .................................................. .................................................. ..........................


1


0



4.1



C


HECK ON


P


OWER


........... .................................................. .................................................. .................................................. ........ 10



4.2



M


AIN


F


RAME


M


AINTENANCE


< p>
............................................ .................................................. .................................................. ............ 10



4.3



P


ROBE


M


AINTENANCE


..... .................................................. .................................................. .................................................. ......... 10



CHAPTER 5 KEYBOARD FUNCTION & TRACK BALL


........ .................................................. .................................................. ...............


1


1



5.1



I


NSTRUCTION OF KEYS UNDER


S


CREEN



................................................. .................................................. ..........................................


1


1



5.2



I


NSTRUCTION OF KEYS ON KEYBOARD


.............................. .................................................. .................................................. .............


1


1



5.3



T


RACK


B


ALL


&L


EFT


&R


IGHT KEY


...... .................................................. .................................................. ........................................... 16



CHAPTER 6 OPERATION PROGRAMMER


............................ .................................................. ................................................


1


7



6.1



S


T ART


-


UP


.......... .................................................. .................................................. .................................................. ...................... 17



6.2



G


ENERAL


M


EASUREMENT


..... .................................................. .................................................. .................................................. .... 17



6.2.1 Distance measurement ...................................... .................................................. .................................................. ............... 17



6.2.2 Perimeter & Area measurement


.......... .................................................. .................................................. .............................. 17



6.2.3 Volume measurement


... .................................................. .................................................. .................................................. .. 18



6.2.4 Angle measurement


........................... .................................................. .................................................. ............................... 19



6.2.5 HR measurement




only for



B/M and M




mode



.......................... .................................................. ........................... 19














































6.3



O


BSTETRIC


M


EASUREMENT


< p>
.


................................ .................................................. .................................................. .........


1


9



6.3.1 BPD-WT Measurement


... .................................................. .................................................. .................................................. 19



6.3.2 CRL measurement


.


.............................. .................................................. .................................................. ............................. 20



6.3.3 GS measurement


.


............................................. .................................................. .................................................. ................ 20



6.3.4 FL-WT measurement ................................ .................................................. .................................................. ........................ 21



6.3.5 HC-WT measurement ............... .................................................. .................................................. ........................................ 21



6.3.6 AC-WT measurement . .................................................. .................................................. .................................................. .... 21



6.3.7 EDD Calculation & Operation Method ................... .................................................. .................................................. ............ 21



6.3.8 AFI measurement ...................................... .................................................. .................................................. ....................... 21



6.3.9 EDD&WT Average measurement


.


................................. .................................................. .................................................. .... 21



6.4



A


NNOTATION


...... .................................................. .................................................. .................................................. ...................... 22



6.5



L-


ZOOM


.......... .................................................. .................................................. .................................................. ......................... 23



6.6



USB

.


.................................... .................................................. .................................................. .................................................. ... 23



6.7



C


INE


L


OOP


.................................... .................................................. .................................................. ............................................. 24



6.8



F


LASH IN


&F


LASH


O


UT



.< /p>


........................................ .................................................. .................................................. ....................... 24



6.8.1 Image permanent storage and output


................................ .................................................. ......................


2


4



6.8.2 Image temporary storage and output


................................ .................................................. .......................


2


4



CHAPTER 7 TRANSPORTATION & STORAGE



.................... .................................................. .................................................. .


2


6



7.1



T


RANSPORTATION



.


............................. .................................................. .................................................. ......................................... 26



7.2



S


TORAGE


.


.................................... .................................................. .................................................. .............................................. 26



CHAPTER 8 EXAMINATION AND CLEARANCE OF SIMPLE FAULT



.< /p>


........................................ .................................................. ..........


27



8.1



E


XAMINATION


< p>
............................................ .................................................. .................................................. ................................. 27



8.2



F


AULT CLEARANCE


< /p>


.


............................ .................................................. .................................................. ......................................... 27



CHAPTER 9 SERVICE GUIDE


................................. .................................................. .................................................. ..........................


28



APPENDIX 1 OUTPUT SOUND POWER OF PROBE


........... .................................................. .................................................. .............


29



APPENDIX 2 MARKED FIGURE AND SIGN ANNOTATION


............................ .................................................. .....................................


32



APPENDIX 3 PACKING LIST



.


... .................................................. .................................................. .................................................. ........ 33














































Chapter 1 Overview




1.1 Characteristic


The


high


resolution


Ultrasonic


Diagnosis


Equipment,


controlled


by


computer


and


equipped


with


digital


screening


converter


(DSC),


is


characterized by its clear image, stable performance and high resolution with adopting variable aperture, multi- segment dynamic focus,


large dynamic band low-noise pre-amplifier, logarithmic compression, TGC control, dynamic filter, edge enhancement and frame-related


technologies etc.


1.2 Classifications




a) The scanning modes of ultrasound are electron convex array and electron liner array.



b) The Ultrasonic Diagnosis Equipment is a Laptop one in accordance with its structure.


1.3 Components of structure


The


instrument


is


consist


of


mainframe,


probe


and


monitor,.


It


can


be


connected


with


medical


image


work


station,


printer,


and


color


monitor. The scanning modes are electron convex array and electron liner array. The main probe is 3.5MHz



R=6 0




Electronic Convex


Array Probe, the optional probe are 6.5 transvaginal probe and7.5 MHz high frequency linear array p


robe.


1.4 Operation functions of Equipment













































Four display format: B


< p>
B+B



4B



B+M



M; Image grey scale: 256 levels




Freezing, real time, selective enlargement, upwards/downwards and left/right turnover of the image can be realized




8 stage TGC adjustment.




18 types of body mark




Soft reset function




Full-screen character annotation




Fixed character, real time clock and calendar




Electron focusing, free combination of focus




Various probe for choice, enough to meet requirement of clinical diagnosis




Frequency Conversion: 2.0MHz




8.0 MHz




Image magnification:


×


1.0

、×


1.2


、×


1.5

< p>
、×


2.0. the utmost detective depth is 240mm




Measuring: distance, perimeter, area, volume, pregnant weeks etc. heart rate and slope can be measured under M mode




Built-in


DSTN


Processor,


PAL-D


and


VGA


video


transmission, external


screen


monitor,


colorful screen,


video tape


recorder,


video


image printer etc.




Movie replay function, uninterrupted replay or step forward/backward replay for 256 images can be realized.




Having the function of



flash in



,



flash out



,



dram in



,



dram out



and



USB






With the optional function of 4 segments frame correlation


3












































1.5 Scope of Application


The equipment is targeting hospital and clinic to diagnose human liver, gallbladder, spleen, kidney, pancreas,


heart,


bladder,


womb,


and


urinary


system


and


it


can


also


be


applied


to


check


intrauterine


equipment,


pregnancy etc.


1.6 Contraindication


The equipment can not be applied to the part where is burnt, scalded or the surface texture is damaged.


1.7 Standard



The equipment is designed and produced in strict accordance with GB10152-1997 B Type Ultrasonic Diagnosis Equipment, GB9706.1



1995 First Part of Medical Electric Equipment in General Requirements for Safety, GB9706.9



1997 Medical Electric Equipment: Safety of


Medical


Ultrasonic


Diagnosis


and


Custodial


Care


Facility


Special


Requirements,


The


equipment


is


the


B


Type


Ultrasonic


Diagnosis


Equipment at Class B, and Type B, Class I in terms of protection from shock hazard


1.8 Commitment to products




safety


We promise that our company shall be responsible for the safety and validity of products which are produced and sold by us .If fals, we are


willing to bear the related economic and legal responsibilities and all the consequence arising therefrom.




Environmental


test


of


the


equipment


meets


the


requirement


of


group



of


climate


environment


test


and


group




of


machinery


environment test of GB/T14710



93 Environmental Requirement & Test Method upon Medical Electric Equipment.


I




Construction to the equipment



s external indicator:






Indicator for the Equipment




Attention! Please refer to the User



s Manual


ON



|











Main Power Indicator


OFF



O










Main Power off Indicator


Video Input Indicator


Video Output Indicator






Protective Earth Indicator









4












































Chapter 2 System Introduction



2.1 Technical Specification


The main functions of the main probe


2.1.1 The frequency of Electronic Convex Array probe is 3.5MHz



R=60





2.1.2 Depth display:



190mm


2.1.3Resolution (vertical direction):



1mm (depth



130mm)


































2mm (130mm



depth



160mm)


2.1.4 Resolution (cross direction)



2mm (depth



130mm)



































3mm(130mm



depth



160mm)


2.1.5 Precision of geometric position :cross direction



10%;



vertical direction




5%


2.1.6 Blind Zone



mm



:




4mm


2.1.7 The conversional frequency points of the main probe (3.5MHz Convex Array probe) are: 2.0MHz



3.5 MHz



4.5 MHz



5.0 MHz



5.5 MHz



6.5 MHz



7.5 MHz , the detailed requirements of the conversion frequency points are as follows:


Chart 1 Required performance functions of Ultrasonic Diagnosis Equipment


The


frequency


of


probe( MHz)


f



2.5


2.5



f



4.0


4.0



f

< br>≤


5.0


5.0


< p>
f



10



(intra-cavity


probe




R


convex


Array)



1


(depth



40)



60mm


liner array ,


Type of probe


R



60mm


convex


array


liner array ,


R



60mm


convex


array




2 (depth



130)



3


(130



depth



160)



1 (depth



130)



2


(130



depth



170)



4



190


Lateral



10


Vertical


direction



5


liner array ,


R



60mm


convex array



Superficial



R



60mm


convex array



Resolution(


lateral


)


mm



3 (depth)



130)



4(130



depth


160)



2


(depth



60)



1


(depth



60)


Resolution


direction)mm


(vertical



1 (depth



130)



2


(130



depth



170)



4



190



1


(depth



80)



3



120


Lateral



10


Vertical


direction



5



1


(depth



80)



3



80


Lateral



5


Vertical direction



5



1


(depth



40)



5



60


Lateral



10


Vertical


direction



5


Blind zone



mm


Utmost


display



mm


Precision


of


depth


Lateral



10


Vertical direction



5


geometric position



%



2.2 Function requirements and frequency conversion points of optional probes


2.2.1 6.5MHz(R=13) intra-cavity probe : 5.5 MHz



6.5 MHz



7.5 MHz


2.2.2 7.5MHz liner surface probe : 7.5 MHz



8.5 MHz



10.0 MHz


2.3 Power


When AC 220V


±


22V or 110V


±


11V is changed , the equipment can also be operated as usual.


2.4 Working time



The continental working time for the Ultrasonic Diagnosis Equipment is more than 8 hours


5












































2.5 Ultrasound output power (in the appendix 1)


2.6 Optional configuration


The medical image work station can be connected with the ultrasonic if the function index of the former satisfies the requirements of the


standard.


2.7 Safety


There are 60 items of Security Detection Project adapts to the portable Ultrasound in the


Appendix 1


2.8 Environmental adaptation



It


shall


satisfy


all


the


requirements


of


Climate


environmental


testing


group




and


Mechanical


environmental



group



which


are


specified in the GB/T14710.



2.9 Basic Circuit Diagram



























































Probe



Receiving Order,


Focus Enlargement


Relevant Treatment


A/D


Type M Address


Injection


Control


Video sync




















































Video Systemization

























Order






Crystal







































Mouse


FRAME


Type B


CPU


Image &


Character


D/A



Gray Scale


Reading/Writing Control


Operation Panel




Monitor




Power Source




































2.10 Basic Principle


Ultrasonic Diagnosis Equipment is, on the basis of different density and ultrasonic transmission speed, and different acoustic impedance


(product of media density and velocity of sound), to regular electric impulse actuate piezoelectric wafer (transducer), ultrasonic at some


frequency is produced, injecting the ultrasonic (sound wave) into human body,


reflection echo will be produced via different viscera



s


interface,


then


the


reflection


echo


can


be


absorbed


by


the


transducer


injecting


such


ultrasonic,


when


the


transducer


will


convert


the


reflection echo (sound wave) to electric impulse, which after enlargement, examination and digital scanning, shall become standard video


signal and display the intersection image of the organ on the screen of the monitor.





6












































Chapter 3 Equipment Installation



3.1 Requirement on Environment


3.1.1 Range of Ambient Temperature: +5




+40




3.1.2 Range of Relative Temperature: ≤80%



3.1.3 Range of Atmospheric Pressure: 800hpa



1060hpa


3.1.4 Supplied voltage: AC 220V±


22V or AC110v ±


11v


3.1.5 Supplied frequency: 50Hz±


1Hz or 60 Hz±


1Hz


3.1.6 The screen should be far away from strong electric field, high magnetic field equipment and high pressure equipment, and direct


sunshine shall be avoided. Sunshine should be avoided indoors, beneficial for image observation, ventilating, moisture proof


and dust


proof.


3.2 Requests of appearance


3.2.1 The surface of Diagnostic Equipment should be clean and beautiful color evenly; no scratches, dirt and oil damage. It is prohibited


to have the bad phenomenon of blistering, peeling, cracking and white


3.2.2 The characters and logos on the panel should be clear, durable. Besides this, the keyboard and mouse should be flexible and


effective.


3.2.3 The control and adjusted parts should be flexible and reliable,




3.3 Check-up after unpacking carton


After unpacking, the equipment should be inspected according to



Packing List



, and should be installed according to requirements and


methods of the



Installation Procedure




and methods of the



Installation Procedure.




3.4 Installation



3.4.1 Laptop Connection Diagram


USB


USB


VGA output



VGAoutput


PAL


PAL




P


. switch


Landlin


e


7


outlet


outlet


PRIN


T


Fuse


fuse















































Power Connection


Inspect the equipment



s power source, after confirming it is within the range of power source, insert one end of the power line into the



Power Socket


ensure safe earth of the B Type Ultrasonic Diagnosis Equipment.




Video Output


Connect Q9 plug, one end of the video line with the



video output




socket of the equipment



s back panel, and connect another end with


the screen or the image processing equipment.




Connection of RDL



96 Probe Connector


First, set the set bar on the probe connector to



Open




position, insert the location pin straight into the location hole on the gang socket,


then set the set bar on the probe connector to



Lock




position, finishing the connection between the main frame and the probe.


Connector plug


Orientation bore


Orientation cancel


lock hole


Connector pin


undo


Set bar

















































The drawing out line of probe connector


Warning:


1. Don



t move or insert the plug of the connector for fear of damaging the probe and main frame; once the probe and the main frame are


connected, please do not move or insert the probe for fear of causing loose contact. Moving or inserting the probe can be conducted only


when the machine is shutdown.


2. For double probe faucet machine, the lower one of the two faucets is the standard probe opening, the higher one is the selective probe


opening. Misconnection should be avoided by all means.




Installation VGA Output


The equipment, equipped with DSTN processing module, can display image on colorful screen by inserting VGA input plug of the colorful


screen or line-by-line screen into the



VGA Output




socket on the back panel and tightening it, and then inserting the power source plug


into the standard three pins socket of the power source.


8












































3.5 Grounding Protection


The equipment



s power source socket should be the standard three pins socket, and the earth point (terminal) under its protection should


be connected with the earth lead.


If


the


power


source


socket


is


under


no


protection


or


disconnected


with


the


power


supply


system


and


protective


earth


system,


the



Protective Earth




shall be conducted. Users shall apply a metal lead with sectional area no less than 1.0mm to connect



earth rod




on one end and ground wire on another.



Note: ground wire shall be laid by users according to relevant standard or under the guidance of skilled electrician.






































9













































Chapter 4 Check & Maintenance



4.1 Check on Power



The


equipment



s


power


source


shall


be


examined


frequently,


and


the


machine


should


not


be


opened


when


the


mains


voltage


is


exceeding the applicable range of the equipment (



AC220V


±


22V 50Hz


±


1Hz



.




The power lead and probe cable of the equipment should be examined



Frequently, and there



s any damage or split, then replacing is needed.




Whether the protective grounding line of the Equipment is connected to the ground or not every time before open the machine.


4.2 Main Frame Maintenance




The equipment



s use environment should meet the requirement of 3.1.




The


outer


covering


can


be


cleaned


with


alcohol


cotton


ball


only


when


the


equipment


is


closed;


and


the


internal


part


of


the


equipment can be cleaned with blower after opening its outer covering only when the equipment is closed





The equipment shall not be opened and closed frequently. And if the equipment should be opened immediately after tailing off, 2-3


minutes should be waited to open the machine for fear of damaging the machine.




If the equipment won



t be used for a long time, the equipment should be placed in the packing box in the direction as required,


and stored in the storehouse, and the environment for storage shall meet the requirement of 7.1.


4.3 Probe Maintenance




The probe is the most vulnerable part, it will get damaged when it falls or get collided. When stop diagnosis, it should be put into


the probe box and press



Freezing


”< /p>



key to


freeze




the probe.




The contact agent adopted by the equipment



s probe is



Medical Ultrasonic Adhesion



. And the contents such as gasoline,


salad oil and other chemical solvents are forbidden to be contained in the adhesion.




The probe is the anti-immersion equipment, none conducting liquid can enter the equipment, so the probe shall not be eroded; the


part in water of the probe shall not exceed 5mm, and the probe shall be examined frequently lest liquid should damage the internal


components.




Cleaning, sterilization and antisepsis: after diagnosis, the probe should be cleaned, sterilized and disinfected with medical alcohol


cotton ball, then properly stored. Please use the thinner, the organic substance to clean the probe.




Once connected with the main frame, the probe shall not be disassembled for fear of defect of contact of probe



s slug and socket.


When using, please do not pull the probe



s cable transmission line,



or sheath of the connector shall escape and cause disconnection.




Probe



s Temperature: when ambient temperature is 25



, the probe



s surface temperature shall not exceed 41



, or when


ambient temperature is lower than 25



, the probe



s surface temperature shall not exceed 16



; for intra-cavity body probe, when


ambient temperature is 25



, the intra-cavity body probe



s surface temperature shall not exceed 50



,above the temperature, the


housing probe shall be forbidden to use for fear of causing scalding.


10












































Chapter 5 Keyboard Function & Track Ball



5.1 Instruction of keys under Screen









Press this key to let the system adjust image automatically


MENU


AUTO















Display different menu



/




Press the two keys to choose menu or increase and reduce the numerical value












SELECT
















Make sure the selected menu


5.2 Instruction of keys on keyboard


























Figure 1 Outline Drawing of Keyboard



1. A-Z Character Key


2.





Adjust the scanning depth





3.



Space Bar. Press the key, space will be displayed in the cursor position.


4.



Enter Key.



11













































5.




For numeric character & direction. Numeric character can be applied to clock adjusting, date


labeling, case history number notation, age, measurement, selection of menu function, selection of focus of electric


focusing.



6.


I n



B/M




mode, two keys can realize left and right movement of puncture line; in the process of movie



s single


frame replay, the single frame image can be replayed forward/backward.




7.



For the speed of cursor movement


8.


For conversion. In the process of distance measurement, it can exchange the starting point or end point of movable


cursor.




9.



For clearing the present measuring result, body sign and text information.


10.


For inputting the common information, such as ID, name, gender and age


Press the key and activate the annotation menu, which will appear in the center of the screen.





AL



T




12













































Annotation Menu



11.


For probe Conversion, you can press the key to convert appropriate probe to selected working interface; the current


probe type and frequency will appear in the right part of the screen, and continuous pressing the key, the probe type


will be changed.



12.



For frequency conversion.


13.



For movie replay


14.




Focus Selection Key.


15.





System reset. Press the key to back the original state when the system halted.



16.



Image Magnification Selection Key, the equipment has 4 types of image magnifications


×


1.0


,×


1.2< /p>


,×


1.5


,×


2.0.



17.



Partial magnifications key


13

全彩-finisher


全彩-finisher


全彩-finisher


全彩-finisher


全彩-finisher


全彩-finisher


全彩-finisher


全彩-finisher



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