Ultrasound Diagnostic Instrument
Service Manual
Volume 1
English Version
Document Number: MN2-2064
Document Revision: 0
Copyright© Hitachi Aloka Medical,Ltd.
F37 Service Manual VOLUME 1
Contents of F37 SERVICE MANUAL VOLUME 1
MN2-2064 Rev.0
PAGE
Chapter 1
INTRODUCTION page 1-1~1-10 (10 pages)
1-1 Service Manual···················································································· 1 — 1
1-2 Contents of this Service Manual·························································· 1 — 1
1-3 Construction of This Service Manual··················································· 1 — 1
1-4 Contents of Each VOLUME/Chapter ·················································· 1 — 2
1-5 Precautions Against Electrical Hazards················································ 1 — 3
1-6 Precautions Against Mechanical Hazards ············································ 1 — 3
1-7 Precautions Against Germ Hazards······················································ 1 — 4
1-8 Precautions to ensure safety of software·············································· 1 — 4
1-9 Precautions for software safety of maintenance tools ·························· 1 — 5
1-10 Precautions regarding handling of patient data ···································· 1 — 5
1-11 Preparation to be made before visit customer ······································ 1 — 5
1-12 Care to be taken in the F i e ld································································ 1 — 6
1-13 Handling of PCB················································································· 1 — 6
1-14 WEEE Directive and RoHS Directive ················································· 1 — 6
1-15 EMC and EMI····················································································· 1 — 7
1-16 System Symbols·················································································· 1 — 8
Chapter 2
Chapter 3
SERVICE PROCESS page 2-1~2-12 (12 pages)
2-1 Repair work on the description of Service Manual······························ 2 — 1
2-2 Upgrade work on the description of Service Manual··························· 2 — 6
INSTALL/DISASSEMBLE page 3-1~3-76 (76 pages)
3-1 How to use this Instruction·································································· 3 — 1
3-2 Disassembly Instruction ······································································ 3 — 3
F37 Disassembling Instruction ···························································· 3 — 4
1. Parts Identification / Individual Unit Layout································· 3 — 5
2. Dismounting Flowchart ································································ 3 — 6
3. Removing of Covers, Pedal, Dust Filter and Fan ·························· 3 — 7
4. Removing of Operation Panel [PNL- F 37* ]··································· 3 — 19
5. Removing of Power Supply Unit [EU-6052*], AC Outlet[JB-290*]·· 3 — 31
6. Removing of PCBs and HDD ······················································· 3 — 33
7. Removing of Digital Imaging Unit [USM-38*] and Motherboard· 3 — 37
8. Removing of B/W Printer, Color Printer and DVD recorder ········· 3 — 45
9. Removing of Probe Holder, Cabl e Hanger, Speaker and Panel Base 3 — 47
10. Removing of Monitor ··································································· 3 — 57
11. Removing of Tilt Ass embly ·························································· 3 — 65
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12. Removing of Panel Arm and Foot Switch····································· 3 — 71
13. Removing of Caster······································································ 3 — 73
14. Removing of Physiological S igna l Unit ········································ 3 — 75
Chapter 4 PRINCIPLE OF SYSTEM OPERATION page 4-1~4-40 (40 pages)
4-1 System Specifications·········································································· 4 — 1
4-1-1 System Summary································································· 4 — 1
4-1-2 Probe···················································································· 4 — 2
4-1-3 Tx/Rx part············································································ 4 — 2
4-1-4 B/W Beam Proces s part ······················································· 4 — 3
4-1-5 Doppler Beam Process························································· 4 — 4
4-1-6 Color Beam Process····························································· 4 — 5
4-1-7 Image Processor / Video Processor part ······························· 4 — 6
4-1-8 Image Display Functions ····················································· 4 — 6
4-1-9 Physiological Signal Display Unit········································ 4 — 7
4-1-10 Digital Data backup / Output ··············································· 4 — 7
4-1-11 Patient Information Management········································· 4 — 8
4-1-12 Display information····························································· 4 — 8
4-1-13 Measuring Function····························································· 4 — 9
4-1-14 Input/Output signal ······························································ 4 — 12
4-1-15 Viewing Monitor ·································································· 4 — 12
4-1-16 Power Supply Unit / Power Consumption···························· 4 — 12
4-1-17 Dimensions / Weight···························································· 4 — 12
4-1-18 Classification of equipment·················································· 4 — 13
4-1-19 Environmental requirements················································ 4 — 13
4-1-20 Applicable standard····························································· 4 — 13
4-2 System Configuration·········································································· 4 — 16
4-3 System Block Diagram········································································ 4 — 18
4-4 Principles of System Operation ··························································· 4 — 23
4-4-1 System Control···································································· 4 — 23
4-4-2 Transmission and Reception block······································· 4 — 27
4-4-3 Backend block ····································································· 4 — 29
4-4-4 Physiological Signal Display unit PEU-F37 (Option) ······· 4 — 35
4-4-5 Power Supply block EU-6052, JB-290, EP5636 ··············· 4 — 36
4-4-6 Viewing LCD monitor IPF-1507······································· 4 — 38
4-4-7 Operation panel PNL-F37················································· 4 — 39
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Chapter 5 TROUBLE SHOOTING page 5-1~5-100 (100 pages)
5-1 Introduction························································································· 5 — 1
5-2 Precautions·························································································· 5 — 1
5-3 Required Tools and Measuring Instruments········································· 5 — 3
5-4 Location of the units and mod ules······················································· 5 — 5
5-5 Default Setting and Statuses ································································ 5 — 9
5-5-1 PSEL···················································································· 5 — 9
5-5-2 TXRX·················································································· 5 — 10
5-5-3 RXBF ·················································································· 5 — 10
5-5-4 Backend··············································································· 5 — 11
5-5-5 Power Supply······································································· 5 — 13
5-5-6 SERVO (Option)·································································· 5 — 13
5-5-7 Maintenance DIP switch ······················································ 5 — 14
5-6 Power supply board EP563600**························································ 5 — 15
5-6-1 How to check power voltage················································ 5 — 15
5-6-2 Operation checks on the Power Supply board EP563600** by itself 5 — 17
5-7 LCD Monitor IPF-1507**································································ 5 — 18
5-7-1 Caution for Monitor repairing·············································· 5 — 18
5-7-2 How to judge the dot defect of LCD monitor······················· 5 — 18
5-7-3 Onscreen display and functions············································ 5 — 19
5-7-4 Monitor troubleshooting ······················································ 5 — 20
5-8 System start-up failure········································································· 5 — 21
5-8-1 Checking the power voltage················································· 5 — 21
5-8-2 Operation step after turn on the machine······························ 5 — 21
5-8-3 Operation step after turn off the machine····························· 5 — 27
5-8-4 System Locking up······························································ 5 — 29
5-9 Error messages···················································································· 5 — 34
5-9-1 Dialog messages·································································· 5 — 34
5-9-2 Assistance messages···························································· 5 — 40
5-10 Ultrasound image error········································································ 5 — 42
5-10-1 Common errors on all display mode····································· 5 — 42
5-11 Network error······················································································ 5 — 43
5-11-1 Check for hardware and software malfunctions ··················· 5 — 44
5-11-2 Checking the network and DICOM environment················· 5 — 45
5-11-2-1 Checking the DICOM settings for the ultrasound machine 5 — 45
5-11-2-2 Checking the DICOM settings for the image server········· 5 — 46
5-11-2-3 Checking the DICOM settings for the Worklist server····· 5 — 49
5-11-2-4 Checking the DICOM printer settings····························· 5 — 52
5-11-2-5 Checking the DICOM settings for the SR (Structured Report) server 5 — 55
5-11-2-6 Checking the DICOM settings for the MPPS server········ 5 — 57
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5-11-2-7 Checking the DICOM settings for the Storage Commitment server 5 — 59
5-11-2-8 Checking the common DICOM settings·························· 5 — 61
5-11-3 Troubleshooting image storage operations··························· 5 — 65
5-11-3-1 Association abort due to transfer syntax mismatches······· 5 — 65
5-11-3-2 Abnormal image display caused by RGB data format······ 5 — 67
5-11-4 Troubleshooting Worklist o per at ions···································· 5 — 68
5-11-4-1 «No Worklist» error due to date setting···························· 5 — 68
5-11-4-2 “No Worklist” error due to search key mismatch············· 5 — 68
5-11-4-3 The handling of institution names during Worklist operations 5 — 69
5-11-5 Network packet monitoring·················································· 5 — 71
5-11-5-1 Preparing packet monitoring software ····························· 5 — 71
5-11-5-2 Starting the packet monitoring software·························· 5 — 75
5-11-5-3 Using the packet monitoring software ····························· 5 — 76
5-11-5-4 Closing the packet monitoring software··························· 5 — 78
5-12 Diagnostic functions············································································ 5 — 79
5-12-1 Ultra-POST, a CPU self-diagnostic tool······························· 5 — 79
5-12-2 Operation panel diagnostic tool············································ 5 — 82
5-12-3 BeHITS self-diagnostic tool················································· 5 — 92
Chapter 6 PERFORMANCE CHECK page 6-1~6-24 (24 pages)
6-1 Introduction························································································· 6 — 1
6-2 Precautions·························································································· 6 — 1
6-3 Creating Service Report······································································· 6 — 1
6-4 Performance Check············································································· 6 — 2
6-4-1 Appearance and mechanism check······································· 6 — 3
6-4-2 Cleaning··············································································· 6 — 8
6-4-3 Equipment information and power voltage check················ 6 — 12
6-4-4 Functional check·································································· 6 — 13
6-4-5 Image quality check····························································· 6 — 16
6-4-6 Safety check········································································· 6 — 19
Ultrasound diagnostic instrument F37 CHECK SHEET······················ 6 — 21
Revision History of the Service Manual
Revision History of VOLUME 1···································································· 1 / 2
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F37 Service Manual VOLUME 1
Contents of F37 SERVICE MANUAL VOLUME 2
MN2-2064 Rev.0
Chapter 1
Chapter 2
Chapter 3
Chapter 4
Chapter 5
Revision History of the Service Manual VOLUME 2
SYSTEM OPERATION
SCHEMATICS
SERVICE INFORMATION
ADJUSTMENT
PARTS LIST
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Chapter 1
INTRODUCTION
APPENDIX
MN2-2064 Rev.0
Chapter 1 Introduction
1-1
1-2
Service Manual
This service manual has been prepared for persons in charge of repair at the field.
This service manual is compiled according to the following basic principle. ”For service, pick out a
faulty PCB and replace it with a new PCB.”
Make the best use of this service manual, making also reference to available technical support
information such as “Technical Bulletin”.
* Technical Bulletin, the Technical Notes, and HISTORY of the equipment which are described on this
manual are released for Service Engineer who has taken appropriate training.
Contents of this Service Manual
The equipment is repaired by PCB replacement. Therefore this service manual does not include the
circuit diagrams of the PCB unit. For the explanation of functions, Block Diagrams and signal list of
each PCB, whose circuit diagram is not included, refer to ”VOLUME 2: Chapter 1 SYSTEM
OPERATION”. The Specification of System and System Block Diagrams are described in “VOLUME
1: Chapter 4 SYSTEM OVERVIEW”.
However, “Cable Connection Diagram”, “Circuit Diagram of PCB equipped with the panel switches
which are easily exchangeable at the field” and ”Circuit Diagrams composed of general circuit such as
Power Supply unit” are described in ”VOLUME 2: Chapter 2 SCHEMATICS”.
For changes and modifications of as well as additions to specifications, if any, prompt information will
be given to you by means of “APPENDIX Manual Change Information”.
zIMPORTANTz Always observe the manner specified for replacement, addition, or deletion of
“Manual Change” to prevent missing of necessary information and keeping of
erroneous information.
1-3 Construction of This Service Manual
The structure of Service Manual is as follows:
VOLUME2 is released for Service Engineer who has taken appropriate training.
VOLUME 1
General instructions on carrying out maintenance service, correspondence at the time of trouble,
procedure that is necessary for operation check are described.
VOLUME 2
Detailed information for actual repair work, available service information are described.
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MN2-2064 Rev.0
Chapter 1 Introduction
1-4 Contents of Each VOLUME/Chapter
VOLUME 1
Chapter 1 INTRODUCTION
Describing the purpose of the Service Manual
Chapter 2 SERVICE PROCESS
Giving information peculiar to the equipment and care to be taken before starting repair work
Chapter 3 INSTALL/DISASSEMBLE
Disassembling Procedure illustrates the disassembly and assembly of main components. Be sure to
follow working procedures if specified
Chapter 4 SYSTEM OVERVIEW
Describing Specification of System and System Block Diagram; It gives the overview of major
signals flows and mutual communication between the units in the system.
Chapter 5 TROUBLESHOOTING
Describing precautions on actual repair work and shows the necessary tools and measuring
instruments. Also, it includes many hints on primary diagnosis and measures to be taken in the
field.
Chapter 6 PERFORMANCE CHECK
Describing the procedure of checking for proper operation after repair and provides the forms of
check sheet.
VOLUME 2
Chapter 1 SYSTEM OPERATION
Describing PCB Block diagram and the Signal List, additional detailed explanation to the
“VOLUME 1: Chapter 4 System Overview”.
Chapter 2 SCHEMATICS
Giving the cable connection diagram including all cables used, the circuit diagram of PCB
equipped with switches and the circuit diagram of and Power Supply unit.
Chapter 3 SERVICE INFORMATION
Providing available information about maintenance service
Chapter 4 ADJUSTMENT
Giving guides for adjustment of PCB and units that are required when they are replaced.
Chapter 5 PARTS LIST
The list of mechanical and electrical parts that is possibly required for repair.
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Chapter 1 Introduction
1-5
1-6
Precautions Against Electrical Hazards
When disassembling the equipment after checking it for a trouble symptom, give care to the following:
1) Be su re to unplug the equipment before disassembly.
2) Be sure to turn off the main switch on the equipment when removing electrical parts such as PCBs,
probe, and cable.
3) Safety alert symbols
4) The indication used on this equipment and in this service manual has the following meaning
“ Indicates a potentially hazardous situation which, if not avoided, may result in minor or moderate
injury. ”
“ A caution message is inserted here. ”
5) Perfectness in grounding, screw tightening, and cover installation is essential. Negligence of it could
cause a possibility of leakage current from outer fitting which may lead to serious damage to a
patient being diagnosed.
Precautions Against Mechanical Hazards
When disassembling the equipment, give care to the following to protect Service Engineer or User from
hazards:
1) Keep the working environment neat.
2) Wear working gloves to protect your hands from getting injured by burrs on the unit and casing.
3) Use only proper tools suited to work being made.
4) Be sure to observe the disassembly procedure shown in VOLUME 2: Chapter 3.
5) Take sufficient care not to damage component with undue load.
6) Be sure to observe equipment is re-assembled properly after disassembly.
7) Use only the specified screws and nuts. Using any other screws and/or nuts would affect not only
mechanical performance, but also electrical performance of the equipment.
In case of the equipment has movable unit internally, take sufficient care not to pinch your hands,
ties, wristbands in movable unit. Be sure to zip-up/fasten your fastener and button. Do not put tools
and screws around movable unit.
9) Take care not to touch Fan when covers of equipment are off.
10) Fix the moving part appropriately when you transport or move the machine. If the machine has
transportation position, set this position appropriately.
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Chapter 1 Introduction
1-7
1-8
Precautions Against Germ Hazards
1) When it is necessary to touch the equipment, options and/or other peripheral devices at a customer
who uses intracorporeal (transesophageal, transurethral, transvaginal, transrectal) probes that need
sterilization, take special care to protect your hands against germs, irrespective of the usage of the
equipment: whether it is used in the operation room or not.
2) Service tools are subject to germ pollution in hospitals and, therefore, need periodical sterilization.
3) Be careful not to directly touch anything assumable to have germ pollution. If necessary, ask the
customer for effective protection against germs.
4) Be sure to confirm the equipment, options and peripheral devices are washed, disinfected or
sterilized appropriately when you take them back from customer site.
5) In case the equipment radiates X-ray, pay attention to the circumference and take care not exposed
X-ray indiscreetly when the equipment is radiating. You must put a film badge for monitoring the
personal exposure at proper position when you do the repair work.
Whenever grease, oil or other chemicals is used for maintenance service, options and/or peripheral
devices, be sure to clean the equipment and/or devices after service work.
Precautions to ensure safety of software
OS (Operating System, such as Windows) operation is allowed Service Engineer who has taken
appropriate training. Illegal change on OS or our program files, Illegal copy of file/folder/partition
which NOT instructed, are prohibited.
Computer controlled medical equipment that involves starting up an operating system from an internal
storage drive could become infected with computer viruses.
Such equipment is usually infected via peripheral storage, media or connections to a network.
Examples detailing route of infection
A) Infections caused during upgrades or maintenance by service engineer.
An infected USB memory device was connected.
An infected floppy diskette was inserted.
A virus-infected USB hard disk drive was connected to remove data.
B) The end user connected an infected USB memory device for presetting, backing up images or
copying.
An infected floppy diskette was inserted.
A virus-infected USB hard disk drive was connected to remove data.
1) Scan all media for viruses before connecting them to or inserting them in the equipment.
2) When an infection is detected, investigate the route of infection and its scope before removing the
virus.
3) An y connections to a network should as far as possible be routed via a firewall.
4) Software, files or services other than those designated by us must not be installed on or uninstalled
from the equipment. Nor must files other than those specified by us be modified or edited.
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Chapter 1 Introduction
1-9
1-10
Precautions for software safety of maintenance tools
These maintenance tools refer to the laptop computers and auxiliary storage devices that service
engineers carry around. (Any computer used for creating CD-Rs for installing upgrades is also regarded
as a maintenance tool.) Thus maintenance tools will include laptop computers, floppy diskettes, USB
memory devices, external hard disks, CD-Rs, etc.
1) Perform a virus scan of any tool that will be used to ensure that they are not infected by computer
viruses.
Regularly perform virus scans of maintenance tools.
2) In unavoidable cases when for some reason safety cannot be confirmed, or when an unknown
computer or memory device is connected, be sure to perform a virus check after use.
3) Update with the most recent virus pattern data prior to performing a virus scan.
4) If a virus scan does not remove the cause for anxiety, use another virus scanner to check.
Precautions regarding handling of patient data
Extreme care must be taken to ensure that data (image data, patient database, DICOM communication
log files) that has been saved to another media during equipment repair and may include patient data is
guarded against leakage, loss and theft. Delete any data that is no longer needed.
1) Work involving use of patient data should be performed in a room that can be locked to prevent
leakage, loss or theft of such data.
2) Such data must be stored in a locked shelf or similar container.
3) If no lockable shelves are available, encrypt the files to reduce possible harm in the event of theft,
leakage or loss.
1-11
Preparation to be made before visit customer
1) When called by a customer on the telephone, note the followings:
• Name of equipment
• Serial number of equipment
• Name of hospital
• Telephone number
• Name of person in charge
• Detail of trouble symptom as far as possible
• State of connection to optional devices
2) Go over the “Technical Bulletin” and “Technical Notes” to see whether the complained trouble can
be mended by means of regular repairing method.
1 — 5
MN2-2064 Rev.0
Chapter 1 Introduction
1-12
1-13
Care to be taken in the Field
1) Check for trouble symptoms.
2) Check for connection to optional devices and other peripheral devices.
3) Record structure of the equipment such as Software Version.
4) After working, restore the equipment according to the above mentioned contents of memory if
necessary.
5) After completion of work, put back the peripheral devices to the original condition.
Handling of PCB
It is our policy that neither repair nor modification of PCBs used for S.M.D. is made in the field as a
rule because of the following reasons:
[REMARKS]
PCB does not need repairing or modifying in the field as a rule.
When handling a PCB, do not touch the IC unless it is necessary.
IC soiled with worker’s hands may cause corrosion. Additionally, foreign particles such as fine solder
dust could be the cause of short-circuited IC lead wires whose pitch is smaller than that of the traditional
ones.
Do not give excessively large shocks to the PCB.
Very thin wiring patterns require extreme care in handling of the PCB.
When replacing the ROM (Read Only Memory) on the PCB, attempting to force the ROM into its
socket would cause the PCB to be subjected to an undue force.
Reuse of chip devices (including resistors, capacitors, diodes, etc.) is strictly inhibited.
z CAUTION z When handling a PCB, avoid touching the IC and connector pins on the devices
to prevent ESD (Electro Static Discharge) damage.
A service person should preferably wear an ESD wrist strap correctly grounded
when handling a PCB.
1-14 WEEE Directive and RoHS Directive
About WEEE Directive
Symbol Meaning
Applied to WEEE Directive. Equipment which has this label must be rejected or
recycled by manufacturer.
WEEE(Waste Electrical and Electronic Equipment) was adopted Feb 2003 by
European Union. The purpose of this directive is to prevent incidence of waste of
electrical and electronic devices and in order to reduce rejection, “re-cycle”,
“re-use” and/or “re-cycle in other way” are demanded.
1 — 6
MN2-2064 Rev.0
Chapter 1 Introduction
About RoHS Directive
RoHS(Restriction of Hazardous Substances) Directive was adopted in Feb 2003 by European Union. It
is closely related to WEEE Directive. This directive restricts the use of hazardous materials in various
type of electronic and electrical equipment.
The PCBs (printed circuit boards) inside and other parts use lead-free (Pb free) solder and lead-free
RoHS compliant components.
Principally it is prohibited to do remodeling or adaptation on PC board, except when there is instruction
by Aloka. Use lead-free solder for soldering internal boards, components and cables.
Do not use old solder that contains lead. It has a different melting point from lead-free solder and must
not be used.
9 Melting point Eutectic solder around 183 Celsius
Lead free solder around 217 Celsius depends on content ratio
Use the label shown above for products
containing only RoHS compliant mounted
components that are soldered using lead-free
solder
Use the label shown above for products that
contain some RoHS compliant mounted
components that are soldered using lead-free
solder.
1-15 EMC and EMI
EMC (Electro-Magnetic Compatibility):
In order to apply EMC standard, following two Electromagnetic interference must have balance and
compatibility.
EMI (Electro Magnetic interferences): An interferences generated from electronic and electrical
•
equipment.
Immunity: Tolerance against external Electromagnetic interferences.
•
z CAUTION z DO NOT execute unnecessary or un-indicated modifications. It would be a cause
of electromagnetic wave occurrence or/and reduction of Immunity.
1 — 7
MN2-2064 Rev.0
Chapter 1 Introduction
1-16 System Symbols
Symbols used by Aloka are described below, together with reference to IEC publication(s).
No. Symbol Meaning
1
2
Danger
Carefully read the pertinent items in the operation manual, and handle the
equipment with grate care.
ANSI standard Z535.3
IEC60601-1, Attached table D
BS 5378 PART1， Appendix A
Biohazard
ANSI standard Z535.3
ISO7000 No.0659
BS 5378 PART1， Appendix A
3
Be careful of explosion
4
5
6
7
8
9
Be careful of electric shock
ANSI standard Z535.3
BS 5378 PART1， Appendix A
Be careful of fire
BS 5378 PART1， Appendix A
Be careful of acoustic power
Type BF applied part
IEC60601-1, Attached table D
Indicates the ON position of the switch.
IEC60417-5007
Indicates the OFF position of the switch.
IEC60417-5008
10
11
Indicates the STAND BY position of the switch.
IEC60417-5009
Alternating current
IEC60417-5032
1 — 8
No. Symbol Meaning
MN2-2064 Rev.0
Chapter 1 Introduction
12
13
14
Potential equalization terminal
IEC60417-5021
Protected against the effects of continuance immersion in water
Labeled on Foot Switch MP-2345B, MP-2614B
IEC60529
Electrostatic discharge (ESD) symbol：
Follow the ESD guide line
1 — 9
MN2-2064 Rev.0
Chapter 1 Introduction
(Blank page)
1 — 10
Chapter 2
SERVICE PROCESS
APPENDIX
MN2-2064 Rev.0
Chapter 2 Service Process
2-1 Repair work on the description of Service Manual
The typical processes for the repair work are shown as the Flow Chart on the next page. Do the repair
work according to this procedure. In the case of modification of the Technical Bulletin, Technical Notes
or Upgrade Kit, see the next item 2-2.
Each procedures of flow chart are numbered to refer its detail shown from page 2-3. Furthermore, the
Flow Chart and its explanation show the time when each section of service manual are required on
repair work. This is a guide for the usage of service manual.
The service manual is very important for the repair work, especially readjustment and performance
check after completion of repair work. This is to keep the safety and quality of equipment. If you make
them, you have to describe that the treatment has been done according to the applied section of service
manual, on the repair report or the like.
The circled numbers shown in the Flow Chart on next page are corresponded to the procedure number
shown from page 2-3.
2 — 1
MN2-2064 Rev.0
Chapter 2 Service Process
Demand of repair
（START）
1
Reception and
Investigation
2
Selection and order of
Required part(s)
Technical Bulletin, Technical Notes
VOLUME 1 Chapter 4, 5
VOLUME 2 Cha
ter 1,2,3
VOLUME 1 Chapter 5
VOLUME 2 Cha
ter 5
Histor
3
Preparation
VOLUME 1 Chapter 2
At your site
At Customer side
4
5
Confirmation
Repair and adjustment
VOLUME 1 Chapter 1, 5
VOLUME 2 Cha
ter 4
6
7
Operation check
Work as normal?
8
Check by customer
Fill repair report
Approve by customer
9
Present repair report
Demand to repair the
defective part(s)
Completion
（END）
Yes
VOLUME 1 Chapter 6
No
10
Repair again
No
11
Show comments of the
prohibition to use on
12
the e
Report to customer
men
Yes
2 — 2
MN2-2064 Rev.0
Chapter 2 Service Process
Procedure 1 Reception of repair and investigation
Accept the repair request from the customer or distributor. At this time, the following points have to be
confirmed and checked,
• Model name/number, and serial number
• Name of customer (Hospital), address, phone number, and name of person in charge
• Configuration of the connection of peripheral devices
• Software version or the like shown on the Maintenance display (if possible)
• Detail of phenomenon appeared on the function of equipment
Make an examination what circuit may be defective as the function of equipment based on the above
information. If you need to know about the basic operation and special information for the maintenance,
refer to the following sections, or ask to the Technical Support,
♦ VOLUME 1 Chapter 4 SYSTEM OVERVIEW
♦ VOLUME 1 Chapter 5 TROUBLESHOOTING
♦ VOLUME 2 Chapter 1 SYSTEM OPERATION
♦ VOLUME 2 Chapter 2 SCHEMATICS
♦ VOLUME 2 Chapter 3 SERVICE INFORMATION
The reported phenomenon may be the original problem on the equipment. Because, refer to the
Technical Bulletin or the Technical Notes separately issued to check it whether defectiveness or not. If it
has been reported as the original problem, make a work according to the Technical Bulletin or the
Technical Notes.
* The Technical Bulletin and the Technical Notes are released for Service Engineer who has taken
appropriate training.
Procedure 2 Selection of required parts and order
If you find the doubtful circuit, order the necessary parts. Then check the delivery date and decide the
date to visit on the consultation with the customer.
For the selection and order of parts, refer to the following sections
♦ VOLUME 1 Chapter 5 TROUBLE SHOOTING
♦ VOLUME 2 Chapter 5 PARTS LIST
For the electrical parts such as UNIT, check the history information on the HISTORY of this equipment
separately issued.
* The HISTORY of this equipment is released for Service Engineer who has taken appropriate
training.
2 — 3
MN2-2064 Rev.0
Chapter 2 Service Process
Procedure 3 Preparation of visiting the customer
Check the required tools, measuring devices and parts to be replaced before the visiting the customer.
Then check the special information for the equipment reference with the following section,
♦ VOLUME 1 Chapter 2 SERVICE PROCESS
Procedure 4 Confirmation of phenomenon
Confirm the appeared phenomenon and condition to happen it with the customer. If you don’t know
about the operation of equipment, refer to the Operation Manual attached to the equipment.
Procedure 5 Repair and readjustment
Repair the defective circuit with the brought parts. For the repair work, read the following section
carefully,
♦ VOLUME 1 Chapter 1 INTRODUCTION
♦ VOLUME 1 Chapter 2 SERVICE PROCESS
And, examine the trouble reason depending on the situation with following section,
♦ VOLUME 1 Chapter 5 TROUBLESHOOTING
The electrical or mechanical readjustment may be requested depending on the replaced parts. Because,
refer to the following section after completion of repair,
♦ VOLUME 1 Chapter 4 ADJUSTMENT
Procedure 6 Operation check
Check the system behavior to keep its condition as same as before in trouble, reference with the
following section. Be sure to do according to the description because check items are depending on the
portion to be treated.
♦ VOLUME 1 Chapter 6 PERFORMANCE CHECK
2 — 4
MN2-2064 Rev.0
Chapter 2 Service Process
Procedure 7 Judgment of the operation quality
If the result of “Procedure 6” is passed to the all standards, do the next “Procedure 8”. On the other side,
if not, make a judgment of “Procedure 10”.
Procedure 8 Confirm by customer, make repair report and approve
Reconfirm the solution of trouble phenomenon with the customer. Then make a repair report and obtain
approval of customer.
The repair report shows not only the treatment but also the method of readjustment and operation check.
If they have been done according to the service manual, the followings have to be shown,
“Readjusted according to the VOLUME 2 Chapter 4 of service manual.”
“Checked according to the VOLUME 1 Chapter 6 of service manual, and passed.”
Procedure 9 Presentation of report and order to repair parts
Fill the repair report with necessary item, and present it accordi ng to the certain procedure.
If the defective parts that trouble cause included is available to use again by repair, make an order to do.
If you cannot judge whether the part can be used again or not, ask to the Technical Support.
Procedure 10 Judgment of possibility to repair again
As the result of judgment on “Procedure 7”, if the trouble is not solved, judge the possibility to make
the repair work again.
If available, return to “Procedure 5” and continue to work.
If unavailable, go to “Procedure 11”.
Procedure 11 Indication of the prohibition to use
As the result of judgment on “Procedure 10”, if you judge that it is impossible to continue the repair
work at this time, indicate that the equipment is still out of order, and also show the prohibition to use,
on the equipment.
Procedure 12 Report to the customer
Report the reason why the trouble cannot be solved to the customer. Then consult about the plan of next
repair work.
And do the same way from “Procedure 2”.
2 — 5
MN2-2064 Rev.0
Chapter 2 Service Process
2-2 Upgrade work on the description of Service Manual
The typical processes for the upgrade work are shown as the Flow Chart on the next page. Do the
upgrade work according to this procedure. In the case of repair work, see the previous item 2-1.
Each procedures of flow chart are numbered to refer its detail shown from page 2-8. Furthermore, the
Flow Chart and its explanation show the time when each section of service manual are required on
upgrade work. This is a guide for the usage of service manual.
The service manual is very important for the upgrade work, especially readjustment and performance
check after completion of upgrade work. This is to keep the safety and quality of equipment.
The circled numbers shown in the Flow Chart on next page, are corresponded to the procedure number
shown from page 2-8.
2 — 6
MN2-2064 Rev.0
Chapter 2 Service Process
Demand of Upgrade
START)
14
1
Selection and order of
requires parts/kits
Technical Bulletin
Technical Notes
Consultation with
Technical Support
Installation Procedure
2
Preparation
VOLUME 1 Chapter 2
At your site
At customer site
3
4
Operation Check
Work as normal?
Yes
VOLUME 1 Chapter 6
No
10
Do the repair work,
according to item 2-1
5
6
7
8
9
Upgrade
Operation check
Work as normal?
Yes
Check by customer
Return unnecessary
parts, and report of
upgrade.
Completion (END)
Installation Procedure
Installation Procedure
VOLUME 1 Section 3
VOLUME 1 Section 6
No
11
Can recover?
12
Show comments of the
prohibition to use on
the equipment
13
Report to customer
Yes
No
2 — 7
MN2-2064 Rev.0
Chapter 2 Service Process
Procedure 1 Selection of required parts / kits and order
Accept the upgrade request from the customer, distributor or person in charge of sales. At this time, the
following points have to be confirmed and checked to decide the parts and kits,
• Document name that announced the upgrade or kit requested
• Model name/number, and serial number
• Name of customer (Hospital), address, phone number, and name of person in charge
• Configuration of the connection of peripheral devices
• Software version or the like shown on the Maintenance display
Make an examination what parts or kits are required based on the above information. For the selection,
refer to the following document separately issued, or ask to the
♦ Technical Bulletin
♦ Technical Notes
To confirm the detail of upgrade, see the Installation Procedure attached with applied Technical Bulletin
or T ech nical Notes.
Technical Support,
Depending on the upgrade, hardware, or software, the other upgrade may be required. Check it with
Technical Bulletin or Technical Notes.
the
Then, confirm the delivery date of required parts or kits, and decide the date to visit on the consultation
with the customer.
* The Technical Bulletin and the Technical Notes are released for Service Engineer who has taken
appropriate training.
Procedure 2 Preparation of visiting the customer
Check the required tools, measuring devices and parts or kits to be used before the visiting the customer.
Then check the special information for the equipment reference with the following section and
document,
♦ VOLUME 1 Chapter 1 INTRODUCTION
♦ VOLUME 1 Chapter 2 SERVICE PROCESS
♦ Technical Bulletin, Technical Notes and/or Installation Procedure
2 — 8
Loading…
Ультразвуковой сканер ALOKA ProSound F37
Производится
Цена по запросу
- Дисплей: Цветной
- Расположение: Стационарный
- Класс: Высокий
- Монитор: 17″ LCD
- Режимы: B, М, D, 2B, 4B, B+M, B+D, B+M+D
- Панорамное сканирование
- 12-битный A/D-конвертер
- Volume Mode
- Broadband Harmonics™
Лучшее предложение для
частных клиник и медицинских центров
ALOKA ProSound F37 – современная ультразвуковая система высокого класса, предназначенная для проведения исследований в области кардиологии, гинекологии и акушерства, ангиологии, эндокринологии, абдоминальных исследований и неонатологии. Данный УЗИ-сканер оснащен LCD-монитором с диагональю 17 дюймов и предполагает цветное допплеровское картирование. Методы сканирования: линейный, конвексный, фазированный секторный.
ALOKA ProSound F37 является одним из самых популярных УЗИ-аппаратов в России, благодаря соотношению разумной стоимости, надежности, широких диагностических возможностей и высокого качества визуализации.
Особенности модели ProSound F37:
- Японская сборка
- Богатая базовая комплектация
- Все типы допплера в базовом комплекте: PW, HPRF, CW, TDI и TDI PW, Flow, eFlow, PowerFlow, DirPowerFlow
- Высочайшее качество визуализации
- Поддержка высокоплотных 192-элементных датчиков экспертной серии
- Большой выбор датчиков
- Небольшие габариты и вес прибора
- Панель управления с регулировкой высоты и угла поворота
- ЖК монитор 17″ со светодиодной подстветкой и матрицей IPS-PRO FUJIFILM (HITACHI)
- 6-кратный ZOOM (опция)
- 12-битный A/D-конвертер (АЦП)
- Панорамное сканирование
- Кинопамять более 1 650 изображений
- Volume Mode — блок трехмерной реконструкции в реальном масштабе времени (4D)
- Индикация информации о пациенте
- Технология широкополостных гармоник Broadband Harmonics™
- Автонастройка яркости панели с учетом освещения в помещении
- Возможность потоковой записи видео исследования в популярных форматах
- 3 порта для датчиков
- Боковой отсек для хранения датчика
- Сменные вкладыши для кнопок
- Алфавитно-цифровая клавиатура с возможностью назначения измерений на любую клавишу
- Достаточное количество держателей кабелей
- Стерилизуемые накладки на нижней части аппарата
- 4 стакана-держателя для датчиков
|
Дисплей |
LCD, ЖК, 17″ |
|
Динамическое фокусирование на всех глубинах |
опция |
|
Доступный объем памяти изображений на жестком диске |
320 Гб |
|
Четыре маркера-измерителя |
есть |
|
4 одновременно включённых динамических фокуса из восьми |
есть |
|
Режимы визуализации |
|
|
Кинопамять |
более 1 650 изображений |
|
Диапазон глубин сканирования |
0,5 – 30 см |
|
Градации цветной шкалы |
128 |
|
Технология широкополостных гармоник Broadband Harmonics™ |
есть |
|
12-битный A/D-конвертер (АЦП) |
опция |
|
Управление внешним принтером с клавиатуры |
есть |
|
Выбор до 45 предустановок |
есть |
|
Индикация информации о пациенте |
есть |
|
Выбор до 5 рабочих частот на датчике |
есть |
|
Градации серой шкалы |
256 |
|
Расчёты |
|
|
Программное обеспечение клинических задач и режимов сканирования |
в т.ч. создание протоколов с расчетом исследуемых параметров в акушерской, гинекологической, урологической, кардиологической и сосудистой программах |
|
Входы/выходы |
для сигналов аудио стерео |
|
Видеовыход DVI-D |
есть |
|
Подключение педали заморозки изображения |
есть |
|
8 USB-разъемов |
для внешней flash-памяти и периферийных устройств |
|
Одновременное подключение 3-х датчиков |
есть |
|
6-кратный ZOOM |
опционально |
|
Потребляемая мощность |
до 900 VA |
|
есть |
65 кг |
|
Количество приемо-передающих каналов |
Более 199 000 |
Технологии УЗ-сканера Aloka ProSound F37
|
DDD |
двойной динамический экран — выведение на экран одновременно двух движущихся В-изображений. |
|
NT (Nuchal Translucency) |
Автоматическое измерение индекса |
|
FAM |
анатомический M-режим (опция) |
|
AutoIMT |
автоматическое измерение комплекса интима-медиа сосуда |
|
Режим для контроля брахитерапии |
есть |
|
eFlow |
улучшенное цветовое допплеровское картирование — высокочувствительный метод отображения кровотока с улучшенным пространственным и временными разрешением. |
|
TDI |
тканевой допплер, отображение движения тканей в цвете. Выбор между режимами «скорости» и «энергии». |
|
AIP |
(опционально) – адаптивное тканеспецифическое улучшение изображения, подавление спекл-шума. |
|
SCI |
компаундное мультилучевое сложно-составное сканирование (опция) |
Производитель:
Hitachi Medical Systems / Aloka
Доступность: В наличии*
Многофункциональный УЗИ сканер HITACHI ALOKA ProSound F37 относится к высокому классу аппаратов ультразвуковой диагностики. Он укомплектован значительным количеством современных режимов, включая ряд экспертных опций, и доступен по цене.
Получить коммерческое предложение
Основные преимущества УЗИ аппарата HITACHI ALOKA ProSound F37
Универсальный аппарат УЗИ HITACHI ALOKA ProSound F37 создан для проведения высокоточных исследований в различных отраслях медицины. Его комплектация включает все основные режимы и функции, а также ряд экспертных опций, в том числе 3D/4D и многолучевое сложносоставное сканирование.
Отдельного внимания заслуживают автоматизированные протоколы расчетов и специализированное программное обеспечение для диагностики в области акушерства, гинекологии, кардиологии, урологии и при исследованиях сосудов. Наряду с технологическими решениями, использованными в сканере HITACHI ALOKA ProSound F37, они помогут специалисту добиться выдающихся результатов при высочайшем уровне визуализации.
Технические характеристики:
- Большой ЖК-монитор с диагональю 17”
- 3 активных порта для подключения датчиков
- 8 USB портов
- Панель управления с регулировкой высоты и угла поворота
- Подсветка клавиш панели управления с автоматической регулировкой яркости
- Ножная педаль дистанционного управления
- Хранение данных в форматах JPEG, DICOM, AVI, TIFF, BMP с возможностью записи на внешние носители
Режимы сканирования:
- Стандартные: B, М, D, 2B, 4B, B+M, B+D, B+M+D
- С цветным доплером: 4B, M, B+B, B+M, B+D
- Дуплексный и триплексный режимы
- Импульсно-волновой доплер PW
- Высокочастотный доплер HPRF
- Постоянно-волновой доплер CW
- Цветной доплер
- Энергетический доплер
- Направленный энергетический доплер
- Тканевой (цветной и спектральный) доплер
- Широкополосная улучшенная тканевая гармоника BbH
- Режим с замедленной синхронизацией DSD для получения изображения движущихся объектов (сердце, кровоток сосудов) в реальном времени на одной половине экране, и замедленное изображение на второй
- Режим DDD для вывода на экран одновременно двух движущихся В-изображений, с ЦДК и без него
- Автоматическая оптимизация изображения и доплеровского спектра нажатием одной кнопки
- Функция eFlow: расширенное цветовое двунаправленное допплеровское картирование для отображения кровотока с улучшенным пространственно-временным разрешением
- Функция SIP для смягчения изображения без потери полезного сигнала
- Функция Needle Emphasis для улучшения визуализации иглы при проведении биопсии
- Функция для контроля брахитерапии
- Пакеты измерений, расчетов и отчетов для различных отраслей медицины
Дополнительные опции и компоненты:
- 3D/4D режим: объемное сканирование в реальном времени; мультипланарная и мультисрезовая реконструкция; псевдорентгеновская реконструкция; автоматическое измерение объемов в 3D
- Функция FlowProfile для анализа профиля потока кровотока
- Функция Flow 3D для анализа кровотока в 3D
- Трехмерная реконструкция методом «свободной руки» FreeHand 3D
- Адаптивное тканеспецифическое улучшение изображения AIP для подавления спекл-шумов
- Функция Auto NT для автоматического измерения индекса NT отека шеи плода
- Функция компаундного мультилучевого сложносоставного сканирования SCI
- Автоматическое измерение комплекса интима-медиа Auto IMT
- Модуль ЭКГ с синхронизацией
- Функции DICOM
- Хранение изображений на CD/DVD носителях
- Водонепроницаемые насадки на коннектор датчиков для дезинфекции полным погружением (опция)
- Технология 4Dshading для фотографического получения трехмерных изображений плода в режиме 3D и 4D
- Опция поддержки специализированных датчиков: трансэзофагеальные, объёмные 3D/4D, конвексные и вагинальные датчики
- Дополнительный порт для карандашных датчиков CW
- Возможность установить по 4 держателя датчиков справа и слева от панели управления
- Вертикальный/горизонтальный держатель вагинального датчика
Датчики:
- Конвексный датчик Hitachi Aloka UST-9130, 1-6 МГц, Абдоминальные исследования, акушерство и гинекология
- Конвексный датчик Hitachi Aloka UST-9115-5, 3-8 МГц, Абдоминальные исследования, акушерство и гинекология
- Конвексный датчик Hitachi Aloka UST-9135P, 1-6 МГц, Абдоминальные исследования, акушерство и гинекология
- Линейный датчик Hitachi Aloka UST-5417, 4-14 МГц | 35 мм, Исследования поверхностных органов, сосуды, костно-мышечная система
- Линейный датчик Hitachi Aloka UST-5045P, 2-6 МГц | 80 мм, Исследования поверхностных органов, сосуды, костно-мышечная система
- Линейный датчик Hitachi Aloka UST-5712, 3-13 МГц | 60 мм, Исследования поверхностных органов, сосуды, костно-мышечная система
- Ректально-вагинальный датчик Hitachi Aloka UST-9118, 2-9 МГц, Акушерство, гинекология, урология
- Вагинальный датчик Hitachi Aloka UST-984, 3-8 МГц, Акушерство, гинекология
- Микроконвексный датчик Hitachi Aloka UST-9133, 1-6 МГц, Абдоминальные исследования, почки, сердце, глубоко расположенные сосуды, мозг, суставы, интраоперационные исследования
- Микроконвексный датчик Hitachi Aloka UST-9136U, 4-13 МГц, Неонатология и педиатрия: абдоминальные исследования, почки, сердце, глубоко расположенные сосуды, мозг, суставы
- 3D/4D конвексный датчик Hitachi Aloka ASU-1014, 1-7 МГц, Трехмерные абдоминальные исследования, акушерство (трехмерное УЗИ плода) и гинекология
- 3D/4D конвексный датчик Hitachi Aloka ASU-1010, 2-10 МГц, Трехмерные абдоминальные исследования, акушерство (трехмерное УЗИ плода) и гинекология
- 3D/4D ректально-вагинальный датчик Hitachi Aloka ASU-1012, 2-8 МГц, Трехмерные исследования в акушерстве, гинекологии, урологии
- Интраоперационный датчик Hitachi Aloka UST-536, 4 -13 МГц, Скелетно-мышечная система, интраоперационные исследования, подкожные структуры, периферические сосуды
- Чреспищеводный датчик Hitachi Aloka UST-5293-5, 2-8 МГц, Чреспищеводная эхокардиография
- Лапароскопический датчик Hitachi Aloka UST-5550, 4-13 МГц, Лапароскопия
- Карандашный датчик Hitachi Aloka UST-2265-2, 2 МГц, Исследования в кардиологии
Клинические изображения:
Купить УЗИ аппарат HITACHI ALOKA ProSound F37 в компании Штейман на выгодных условиях.
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УЗИ аппарат HITACHI ALOKA ProSound F37
Гарантия лучшей цены
DESCRIPTION
Ultrasound System
Smart and clear imaging combined with eFLOW and Auto Angle Correct makes this a small and reliable system for any work environment. Thoroughly simple and compact. As a user-friendly diagnostic ultrasound system full of functional and ergonomic features, F37 is ready to be the user’s partner. The F37’s simple operational features provide an easy and smooth workflow. The necessary controls for routine examinations are intuitively laid out, with high priority on reducing the examiner’s operation steps. Imaging features inherited from higher-class models provide a work environment for concentrated examinations. The F37 delivers outstanding images while maintaining comfort for the patient and the examiner.
FORUMSView All (13)
Ask a New Question
| -TARIK 8 months ago |
8 months agoUser manual Need user manual Equipment: Hitachi ultrasound aloka f37 Reply |
| -Fikyo a year ago |
a year agoHITACHI ALOKA F37 I have this Hitachi Aloka F37 ultrasound machine, at boot up it gives to messages on the screen The first one is «there is not a reply from the SbeInstFEFirm(-1) The second one is DPM_STAT TM Out Err:0×01 3E BP:0×40 Does anyone have an idea of how to resolve this problem. Kindly assist Reply |
| -sametert61 2 years ago |
2 years agooperations panel logs Hello, THE KEYBOARD ON OUR DEVICE SOMETIMES DOES NOT WORK. THE LIGHTS ARE BLINKING CONSTANTLY, BUT THE KEYBOARD IS NOT RESPONDING.CAN YOU HELP ME? Please THANKS?Reply |
DOCUMENTS / MANUALSView All
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FEATURES
- The most advanced broadband beam-forming technology combined with high speed image processing that allows for higher definition ultrasound imaging than ever before.
- Provides high quality imaging using an expanded range of harmonic signals. This technology results in excellent image resolution and sensitivity and improved penetration.
- Clearly displays differences in tissues, reducing speckle noise while maintaining the frame rate. It can also display outlines more clearly by selectively emphasizing boundaries.
- The ultrasound beam is transmitted and received in real time and in the multiple directions resulting in a reduction of speckle noise, suppression of artifacts, and improvement of contrast resolution allowing lesions to be clearly observed
- At the touch of a button the B-mode image is instantly optimized to the user’s preference. This technology continually monitors the user’s typical settings to optimally adjust the image when pressed resulting in less manual adjustments and more efficient examinations.
- The new high-efficiency probes are very lightweight and designed to be high in energy conversion to transmit high-quality ultrasound beams without raising the temperature on the probe surface.
- The image quality contributes to reduction of examination time
- Patient-friendly examinations enabled by the small size of the probe
- Basic measurement results can be transferred onto the report
- Unique probe holder for endocavity probes
Стационарный ультразвуковой сканер для рутинной диагностики в гинекологии, общей радиологии, кардиологии, для интраоперационного контроля и др.
Описание прибора
Hitachi Aloka F37 — цветной полностью цифровой ультразвуковой сканер среднего класса для общих исследований, акушерства, гинекологии и кардиологии и др. Ультразвуковой сканер F37 — гармоничный продуманный внешний облик и хорошие возможности визуализации, ориентированные на ежедневное использование.
Сканер снят с производства. Интересует аппарат с похожими характеристиками? Получите консультацию у нашего специалиста, позвонив по бесплатному номеру 8 (800) 100-52-10 или закажите обратный звонок.
Назначение
Общая радиология (исследование органов брюшной полости и забрюшинного пространства, молочной и щитовидной желез, других поверхностных органов), урология, гинекология и акушерство, ангиология (исследование периферических и магистральных сосудов, флебология, транскраниальная допплерография), кардиология, исследование скелетно-мышечной системы, неврология, интраоперационные исследования, чреспищеводная эхокардиография, неотложная медицина, педиатрия и неонатология, косметология и дерматология, ветеринария.
Характеристики
| Монитор | 15″ |
| Гарантия (мес) | 12 |
| Активные порты | 3 |
| Высокоплотные датчики | Да |
| CW доплер | Да |
| Тканевой доплер | Да |
| Анатомический М-режим | Да |
| 3D/4D | Да |
| Панорамное сканирование | Да |
| Автоматическое измерение комплекса интима-медиа | Да |
| Педиатрические датчики | Да |
| Интраоперационные датчики | Да |
| Биплановые датчики | Да |
| Чреспищеводные датчики | Да |
| Лапароскопические датчики | Да |
Инновационные технологии
- Auto Angle Correction — производит автоматическую корректировку допплеровского угла с соответствующей коррекцией шкалы скоростей кровотока в режиме спектрального допплера.
- LV eFlow – это высококачественный режим отображения кровотока в левом желудочке с увеличенным пространственным и временным разрешением. Режим обеспечивает улучшенную визуализацию границ эндокарда.
- Flow Profile — графическое отображение и количественный анализ профиля потока в выбранном участке сосуда. В результате использования функции врач с высокой точностью и воспроизводимостью получает значение объёма потока крови.
- Брахитерапия — система имеет в наличии специальный режим для контроля брахитерапии предстательной железы.
- Needle Emphasis — обеспечивает чёткую визуализацию иглы за счёт изменения наклона ультразвукового луча и адаптивной оптимизации отображения.
Примеры эхограмм
Hitachi Aloka F37
Примеры эхограмм Hitachi Aloka F37
Датчики
Конвексные
Линейные
Внутриполостные
Микроконвексные
Микроконвексный датчик Hitachi Aloka UST-9133
1-6 МГц
Абдоминальные исследования, почки, сердце, глубоко расположенные сосуды, мозг, суставы, интраоперационные исследования.
Микроконвексный датчик Hitachi Aloka UST-9136U
4-13 МГц
Неонатология и педиатрия: абдоминальные исследования, почки, сердце, глубоко расположенные сосуды, мозг, суставы.
3D/4D объемные
Интраоперационные
Чреспищеводные
Лапароскопические
Карандашные
Похожие товары
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Калькулятор лизинга
Стоимость оборудования
900 000 руб.
900 000 руб. 7 000 000 руб.
Авансовый платеж
180 000 руб./20%
10% 50%
Срок
12
12 месяцев 60 месяцев
руб/мес.
Вопросы и ответы
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Страна производства: Япония
Производитель: Fujifilm Hitachi
Год выпуска: 2023
Гарантия: 24 месяца
Класс: средний
Тип: стационарный
Состояние: Новый
Наличие: Снят с производства
Калькулятор
лизинга
Описание прибора
Характеристики
Инновационные технологии
Примеры эхограмм
Датчики
Похожие товары
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