全彩-finisher
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
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effect your
operating of the product.
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1.
2.
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in the Product
Registration card.
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Thank you for your kind
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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
............................................ .................................................. .................................................. .................... 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
............................................ .................................................. .................................................. ...... 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
............................................ .................................................. .................................................. ............ 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
.
................................
..................................................
..................................................
.........
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
p>
.
.............................
..................................................
..................................................
.........................................
26
7.2
S
TORAGE
.
....................................
..................................................
..................................................
..............................................
26
CHAPTER 8 EXAMINATION AND
CLEARANCE OF SIMPLE FAULT
.<
/p>
........................................
..................................................
..........
27
8.1
E
XAMINATION
............................................ .................................................. .................................................. ................................. 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
、
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
、×
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
Ⅱ
of
climate
environment
test
and
group
Ⅱ
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)
≤
p>
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
<
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
Ⅱ
and
Mechanical
environmental
group
Ⅱ
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
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