JUMONG VET

Installation Manual
 JUMONG VET Manual

Table of Contents

1 Manufacturer ............................................................................................. 3
2 Safety and Regulatory ............................................................................................................................ 3
2.1 Indications for Use.................................................................................................................... 4
2.2 Safety ........................................................................................................................................ 4
2.3 Know the Equipment ................................................................................................................ 6
2.4 Electromagnetic Compatibility ................................................................................................. 6
2.5 Radiation Safety ....................................................................................................................... 8
2.6 Emergency Procedures ........................................................................................................... 10
2.7 Safe Operation Precautions .................................................................................................... 10
2.8 Symbols .................................................................................................................................. 13
2.9 Regulatory Requirements ....................................................................................................... 17

3 Record of Revisions .................................................................................. 19

4 Introduction ............................................................................................. 20
4.1 Introduction ....................................................................................................................................... 20

4.2 Description ........................................................................................................................................ 20

4.2.1 JUMONG VET Components ................................................................................................. 20
4.3 Dimensions (Unit: mm) ...................................................................................................................... 20
4.3.1 Drawing ............................................................................................................................... 20

5 Installation ............................................................................................ 21
1. Table and Pillar assembly .................................................................................................................... 21

2. Console Bracket Assembly ................................................................................................................... 23

3. Console assembly ................................................................................................................................ 24

4. Tube and Collimator Assembly ............................................................................................................ 25

5. Generator and Power Set-up ............................................................................................................... 29

6. Monitor Set-up .................................................................................................................................... 36

7. Detector Calibration ............................................................................................................................ 38

8. Installation Result ................................................................................................................................ 40

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1 M ANUFACTURER
Business name: SG HealthCare Co., Ltd.
Address: 10 Yangnyeong-ro, Moga-myeon, Icheon-si, Gyeonggi-do 17408, Korea
Telephone: +82 (0)31 790 0647
Fax: +82 (0)31 790 0604
Web: www.sghealthcare.com
Mail: sales@sghealthcare.com

2 S AFETY AND R EGULATORY

This chapter explains the safety considerations, general equipment and patient related
precautions, and the symbols used for the safe operation of your equipment. This chapter
also includes information about the emergency procedures.

This chapter presents the concepts necessary to successfully operate your system safely.

Topics covered include:

l Indications for Use

l Emergency Procedures
l Safety
l Safety Operation Precautions
l Know the Equipment
l Symbols
l Electromagnetic Compatibility
l Regulatory
l Radiation Safety
l X-ray Source Assembly Filtration

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2.1 I NDICATIONS FOR U SE

JUMONG VET system is a digital imaging solution designed for general radiographic system
for Veterinary.

WARNING

It is forbidden to use this device to take exposure

repeat and frequently for a same patient, especially a
child.

WARNING

It is forbidden to use this device to take exposure for

pregnant woman.

2.2 S AFETY

The electrical wiring of the relevant rooms complies with all national and local codes, as
well as the Regulations for the electrical equipment of buildings published by the
Institution of Electrical Engineers.
All assembly operations, extensions, re-adjustments, modifications, or repairs are carried
out by SG Healthcare authorized service representatives. The equipment must be used in
accordance with the instructions for use.

WARNING

This X-Ray unit may be dangerous to patient and

operator, unless safe exposure factors, operating
instructions and maintenance schedules are
observed.

To be used by authorized personnel only.

WARNING

Electric Shock Hazard! Do not remove covers or

panels. The Acquisition Console and cabinets contain
high voltage circuits for generating and controlling X-
rays. Prevent possible electric shock by leaving covers

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or panels on the equipment. There are no operator

serviceable parts or adjustments inside the cabinets.
Only trained and qualified personnel should be
permitted access to the internal parts of this
equipment.

WARNING

Only SG Healthcare validated equipment can be

plugged into the interface in any part of this system.
Leakage current requirements of non-validated
equipment cannot be maintained with high
confidence.

WARNING

Never touch patient and any exposed extra low safety

circuits or connectors simultaneously. Electrical shock
may occur.

WARNING

Only table, Detector Stand, digital detector, tube

assembly, collimator and system cabinet which are
specified to be installed in the examination room are
suitable for use in patient environment. Any other
equipment or component specified to be installed in
control room shall not be brought into and use in
patient environment.

WARNING

Radiographic equipment must be operated by

qualified personnel and only after sufficient training.

CAUTION

Always be alert to safety when you operate this

equipment. You must be familiar enough with the
equipment to recognize any

Malfunctions that can be a hazard. If a malfunction

NOTE occurs or a safety problem is known to exist, do not
use this equipment until qualified personnel correct
the problem.

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- CAUTION

It is the User’s responsibility to provide the means for

audio and visual communication between the operator
and the patient.

2.3 K NOW THE E QUIPMENT

Read and understand all of the instructions in this Learning and Reference Guide before
attempting to use the product.

E Q U I P ME N T C L A S S I F I C A T I O N S

The following equipment classifications are applicable to the Learning and Reference Guide
before attempting use the product.

l Equipment classification with respect to protection from electric shock: Class I

l Degree of protection from electric shock: Type B

l Equipment not suitable for use in the presence of a flammable anesthetic

mixture with air or with nitrous oxide

l Mode of operation: Continuous operation with intermittent loading

2.4 E LECTROMAGNETIC C OMPATIBILITY

WARNING

This system is intended for use by healthcare

professionals only. This system may cause radio
interference or may disrupt the operation of nearby
equipment. It may be necessary to take mitigation
measures, such as re-orienting or relocating the
system or shielding the location.

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WARNING

This medial electrical equipment / system needs

special precautions regarding EMC and needs to be
installed and put into service according to the EMC
information provided in the accompanying
documents.

WARNING

Portable and mobile RF communications equipment

can affect this medical electrical system. Make sure
those communication equipment are powered off
before they are taken near this equipment / system

WARNING

Power line anomalies or electrostatic discharges in all

equipment areas may cause the monitor image to
become momentarily disrupted or to go to blank; the
mouse and/or keyboard may become inoperable or
an error may be displayed on the worklist or image
viewer screens. The system may recover by itself or
you may need to reboot the system. The system may
shut itself down, and will require a reboot.

WARNING

A power surge during image transmission to the

workstation after acquisition may cause the image to
be lost. the system

NOTE Will operate normally after the power surge, but the
image must be reacquired.

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WARNING

Power line anomalies or electrostatic discharges to

the system cause a CD/DVD write failure error. A new
CD/DVD should be used and the image re-written.

2.5 R ADIATION S AFETY

Always use the proper technical factors for each procedure to minimize X-ray exposure and
to produce the best diagnostic results. In particular, you must be thoroughly familiar with the
safety precautions before operating this system. Default system techniques are
recommended for AEC acquisition. Default techniques are designed to optimize the image
processing parameters.

CAUTION

Please protect the families and any other company of

the patients’ around this device from radiation. Please
protect the technologists who is around this device
from radiation.

CAUTION

Always use the proper technical factors for each

procedure to minimize X-ray exposure and to produce
the best diagnostic results. In particular, you must be
thoroughly familiar with the safety precautions before
operating this system. Default system techniques are
recommended for AEC acquisition. Default techniques
are designed to optimize the image processing
parameters.

CAUTION

There should be no persons other than the patient in

the exam room during x-ray exposure. If circumstances
require another

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Person to enter the room while x-ray exposures are

NOTE planned or possible, that person should be well
protected in accordance with accepted safety
practices.

CAUTION

Tube assembly and collimator used in this system are

verified to have a total filtration of 2.5 mmAl at least,
whenever you replace one of them, make sure total
filtration for this X-ray equipment is not less than 2.5
mmAl.

CAUTION

Make sure any other accessories or materials are not

located in the primary X-ray beam during exposure
that result in a bad image quality.

CAUTION

Use the largest possible focal spot-to-skin distance

appropriate for the anatomy being imaged, to keep
the patient absorbed dose as small as possible.

CAUTION

Always use protective devices and protective clothing

for the patient, operator or even other persons as
appropriate to the workload and examination
involved.

CAUTION

Hospital is responsible to provide means for audio and

visual communication between the operator and the
patient.

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2.6 E MERGENCY P ROCEDURES

It is not always possible to determine when some components, such as the X-ray tubes, are
nearing the end of their operating lives. These components could stop operating during a
patient examination.

WARNING

Do not use device should a safety problem occur and

contact authorized service immediately.

WARNING

If the radiation is still continuing, switch off the power

to stop the radiation.

2.7 S AFE O PERATION P RECAUTIONS

GENERAL USE WARNINGS

WARNING

Do not load non-system software onto the system computer. This

may cause system to crash.

WARNING

Use of operation methods other than those specified herein may

result in hazardous radiation exposure.

WARNING

For continued safe use of this equipment, follow the instructions

contained in this Learning and Reference Guide. Study this guide
carefully before using the equipment and keep it at hand for quick
reference. It may be desirable for the facility to print this manual
from a standard PC to have a hard copy available within the
Radiology

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WARNING

It is the responsibility of the operator to ensure the safety of the

patient at all times. When the table is in use the patient should be
monitored by visual observation, use of proper patient positioning,
and use of the protective devices provided.

WARNING

Thoroughly check that there is no interference or possibility of

collision between the patient and other equipment.

WARNING

Perform periodic maintenance to ensure continued safe use of the

equipment. Follow recommended preventative maintenance
schedule as outlined in the SG Field Service Manual.

WARNING

Check the Collimator status before using this equipment, to

prevent it falling down.

WARNING

Never exceed the rated load of patient handling devices.

WARNING

If safety problem occurs, please contact Authorized service

immediately.

CAUTION

Always assist the patient during loading and unloading from table.
Keep the patient in full view at all times and never leaves the
patient unattended while on the table.

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CAUTION

Please carefully monitor all equipment motions to prevent

collisions. Attention shall be drawn during operation to prevent
possible injuries that could result from collision of the power-
driven equipment parts with other moving or stationary items
likely to be in the environment.

CAUTION

Please check for obstructions before moving the equipment.

PATIENT POSITIONING WARNINGS

WARNING

During patient procedures, ensure the patient’s head, hands and

feet are completely within the tabletop area. If any portion of the
patient’s body extends over the edge of the tabletop, serious
injury may result.

WARNING

The maximum supported weight, with the tabletop fully extended

toward the head or foot end of the table, is 300kg.Exceeding this
limit may cause equipment damage or injury to the patient.

WARNING

Always, watch all parts of the patient table to verify there is no

interference or possibility of collision with the patient or with
other equipment. When moving the table, cautiously put hand on
table top. Intravenous catheter or other lines connected with the
patient must be monitored to avoid interference during patient
positioning.

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WARNING

When operate the Stand & Table, the operator shall always watch
the patient for the moving parts to avoid injury by collision.

2.8 S YMBOLS

This section explains the symbols used on this system and in its accompanying documents.

X- R A Y T U B E
Table describes the operational symbols for the system such as X-ray emissions and
collimator locations.

Symbol Description

Fluoroscopy X-ray ON indicators

Radiography X-ray ON indicators

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P O WE R ON A N D OFF

A gray POWER ON button is used to turn on the power to the

system.
The button is located on the console.

A gray POWER OFF button is used to turn off the system. The
button is located on the console.

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ELECTRICAL TYPE

Table describes the electrical protection rating based on system type.

Symbol Description

Type B Equipment indicates the equipment provides a particular

degree of protection against electrical shock regarding leakage
current and protective earthling per IEC60601-1.

ELECTRICAL CURRENT
Table describes the symbols for the different types of electrical current that may be used on
your system.

Symbol Description

Alternating Current indicates the equipment is suitable for

alternating current only.

Direct Current indicates the equipment is suitable for direct

current only.

Both direct and alternating currents indicate the equipment is

suitable for both direct and alternating current.

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G R O U N D
Table describes the different types of grounding used in your system.

Symbol Description

Functional Earth (ground) Terminal indicates a terminal directly

connected to a point of a measuring supply or control circuit or
to a screening part, which is intended to be earthed for
functional purposes.

Protective earth (ground) identifies any terminal which is

intended for connection of an external protective conductor to
protect against electrical shock in case of a fault.

Frame or chassis identify the frame or chassis terminal.

C O L L I MA T O R
Table describes the collimator controls and the radiation field.

Symbol Description

Control for indicating radiation field by using light.

Indicates the collimator blades are closed. The controlled blades

are shown in thicker lines.

Indicates the collimator blades are open. The controlled blades

are shown in thicker lines.

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2.9 R EGULATORY R EQUIREMENTS

This equipment generates, uses, and can radiate radio

frequency energy. The equipment may cause radio frequency
interference to other medical and non-medical devices and
radio communications. To provide reasonable protection
NOTE
against such interference, this product complies with emission
limits for Group 1 Class A Medical Devices as stated in EN 60601-
1-2. However, there is no guarantee that interference will not
occur in a particular installation.

NOTE If this equipment is found to cause interference (which may be

determined by switching the equipment on and off), you (or

qualified service personnel) should attempt to correct the
problem using one or more of the following measures:

–Reorient or relocate the affected devices.

–Increase the space separating the equipment and the affected

device.

–Power the equipment from a source different from that of the

affected device.

–Consult the point of purchase or the service representative for

further suggestions.

The manufacturer is not responsible for any interference caused

either by the use of interconnect cables other than those
NOTE recommended or by unauthorized changes or modifications to
this equipment. Unauthorized changes or modifications could
void the user’s authority to operate the equipment.

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To comply with the regulations applicable to an electromagnetic

interface for al Group 1 Class A Medical Device, all interconnect
cables to peripheral devices must be shielded and properly
grounded. The use of improperly shielded and grounded cables
NOTE may result in the equipment causing radio frequency
interference in violation of the
European Union Medical Device directive and Federal
Communications
Commission regulations.

Do not use devices which intentionally transmit radio frequency

(RF) signals (cellular phones, transceivers, or radio controlled
NOTE
products) in the vicinity of this equipment, as it may cause
performance outside the published specifications.

Keep the power to these type devices turned off when near the equipment.

The medical staff in charge of this equipment is required to instruct technologists, patients,
and other people who may be around this equipment, to fully comply with the above
requirement.

DISPOSAL OF WASTE
This symbol indicates that the waste of electrical and electronic equipment must not be
disposed as unsorted municipal waste and must be collected separately. Please contact an
authorized representative of the manufacturer for information concerning the
decommissioning of your equipment. Figure: Disposal of waste symbol

MANUFACTURER’S RESPONSIBILITY
Allow only authorized, properly trained personnel to operate the equipment.

This equipment is sold with the understanding that the manufacturer, its agents, and
representatives do not accept any responsibility for overexposure of patients or personnel to
X-Ray radiation. No responsibility is assumed for any unit that has not been serviced by
qualified authorized service personnel.

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3 R ECORD OF R EVISIONS

Revision History

Version Date Description

1.0 27th of MARCH, 2021 Preparing the manual

1.1 19th of APRIL, 2021 1st edition of manual

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4 I NTRODUCTION

4.1 I NTRODUCTION

This manual provides installation and service information for JUMONG VET system.

4.2 D ESCRIPTION

The JUMONG Vet is a stationary system with 17x17 cassette size detector allows a full range of
chest and other vertical examinations. It is an ideal solution for everyday image examination of
small and big animals.

4.2.1 JUMONG VET C OMPONENTS

- Tube stand & Table, X-ay Tube, Collimator, Detector, Generator, X-ray Control Console
Workstation (Including monitor, keyboard and mouse)

4.3 D IMENSIONS (U NIT : MM )

4.3.1 D RAWING

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5 I NSTALLATION

1. T ABLE AND P ILLAR ASSEMBLY

1.1 Prepare the Table. (*When moving the table, Do not lift by grabbing the table top.
Grab the body of the table when lifting)

1.2 Prepare the table Pillar.

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1.3 Assemble the prepared table and pillar.

(*Attach the pillar to the table by bolting the pillars to the two holes under the table .)

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2. C ONSOLE B RACKET A SSEMBLY

2.1 Prepare the console brackets.

2.2 Level the Console bracket using a leveler

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2.3 After leveling the bracket, tighten the 4 bolts.

3. C ONSOLE ASSEMBLY

3.1 Prepare the Console.

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3.2 Loosen the 2 bolts on the back of the console and fasten it with the console bracket.

4. T UBE AND C OLLIMATOR A SSEMBLY

4.1 Place the tube on the fixed console bracket.

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4.2 Prepare the prepared tube and collimator fixing bracket.

(* Collimator bracket is mounted on the collimator.)

4.3 Place the prepared tube on the console bracket and fix it with the prepared
collimator bracket and 4 bolts.

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4.4 Mount the collimator to the collimator bracket.

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4.5 Connect the installed tube and the collimator to power.

(*When connecting the collimator power, disassemble the tube cover and connect the CM
cable.)

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(*Rotor Cable is pre-connected to the tube)

(*After completing the cable connection, reassemble the cover.)

5. G ENERATOR AND P OWER S ET - UP

5.1 Prepare the generator.

(*After preparing the generator, open the cover.)

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5.2 Connect the cable from the console to the control board.

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(*Please connect the cable properly.)

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5.3 Connect the rotor cable previously connected to the tube to the generator terminal block.

5.4 After preparing the foot switch, connect it to the same terminal block as the rotor cable.

(*Please connect the cables properly after checking the labels.)

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5.5 Connect the power cable for power supply.

5.6 Connect HVC according to polarity. Connect after checking (+,-)

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(*Connect the HVC to the right polarity also with the tube.)

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5.7 After all cables are connected, reassemble the generator cover.

(*After the assembly is complete, place the generator under the table.)

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6. M ONITOR S ET - UP

6.1 Fix the bracket for mounting the monitor on the side of the column.

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(*When the monitor is installed, connect it to the PC.)

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7. D ETECTOR C ALIBRATION

7.1 To do Detector Calibration, the table top must be disassembled.

(*Please remove the bolts under the table.)

(* It is okay to disassemble the table top before installing the product.)

7.2 When disassembling the table top is complete, put the detector in the tray and proceed with
the detector calibration.

(*When the detector calibration work is completed, reassemble the top plate)

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7.3 Install the apron holder.

(*The order of installing the apron holder is irrelevant)

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8. I NSTALLATION R ESULT

8.1 Picture of installation result.

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SG Healthcare Co., Ltd.

10, Yangnyeong-ro, Yangpyeong-ri, Moga-myeon, Icheon-si, Gyeonggi-do,

Republic of Korea 17408

TEL: +82-02-449-6908

FAX: +82-02-449-6909

Home page: www.sghealthcare.com

If you need any technical support, please do not hesitate to contact our service

team: service@sghealthcare.com

EC REP European representative: AeMi World.

Bugenhagenstr.8, 10551 Berlin, Germany

Tel: +49 (030) 8620 3461

Fax: +49 (030) 8620 3789

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