Professional Documents
Culture Documents
Rev 07
Notice: Information contained in this manual is confidential and the property of DRTECH Inc., which is
only provided to the authorized customers of DRTECH Inc. The purpose of the manual is to assist the
users to comprehensively utilize the product of DRTECH Inc. All information contained in the manual
may not be altered or distributed without prior written consent of DRTECH Inc., and may not be disclosed
to unauthorized personnel. Information contained in the manual may be altered without prior notice.
Copyright © 2016 DRTECH Corporation. All rights reserved.
Disclaimer
In no event shall DRTECH be liable for any damage or loss arising from fire, earthquake, any action or accident
by a third party, any intentional negligent action by users, any trial usage, or other usage under abnormal
conditions. Roentgenography, image processing, image reading, and image data storage must be performed in
accordance with the laws of the country or region in which the product is being used. The user is responsible for
maintaining privacy of image data. In no event shall DRTECH be liable for personal physical harm or property
damage that is sustained, under any conditions when the instructions are not followed or the product is misused.
It is the responsibility of attending physicians to provide medical care services. DRTECH will not be liable for
faulty diagnoses. In no event shall DRTECH be liable for direct or indirect consequential damages arising from
the use or unavailability of this product. DRTECH shall not be liable for loss of image data for any reason. In no
event shall DRTECH be liable for any damage arising from moving, alteration, inspection or repair by a person
other than authorized service engineers. Specifications, compositions, and appearance of this product may
change without prior notice.
Thank you for choosing these series of after-service guides that DRTECH publishes as part of its
comprehensive product quality guarantee program.
This service manual consists of four categories; RSM 2430C / RSM 2430C Choice Information,
Function of RSM 2430C / RSM 2430C Choice, Installation of RSM 2430C / RSM 2430C Choice,
Maintenance.
If the product undergoes a large modification, a new service manual of revised edition will be sent to
you. In other cases, updates for the service manual will be sent to you.
Our trained service department staffs are readily available to assist you with all of your service needs.
We will recommend the best way to resolve any problems as quickly as possible.
If you have questions, concerns or need more information, please feel free to contact us at;
DRTECH Corporation
[Headquarter]
2F/6F, SPG dream building, 166, Jeongjail-ro, Bundang-gu, Seongnam-si, Gyeonggi-do, Korea
Tel: +82-31-784-8800
Fax: +82-31-784-8899
[Factory]
Suite No.1 1 Floor/Suite No.2 3 Floor, 29, Dunchon-daero 541beon-gil, Jungwon-gu, Seongnam-si,
Gyeonggi-do 462-807, Republic of Korea
Tel: +82-31-779-7449
Fax: +82-31-779-7490
E-mail: drtech@drtech.co.kr
The following symbols are used throughout the manual. Keep in mind of these to avoid any accident.
Do not ever put any object or press the detector panel strongly.
Safety Symbols
The following safety symbols are found on RSM 2430C / RSM 2430C Choice device components.
Keep in mind of these to avoid any accidents.
Alternating Current
Read and understand all instructions and warning labels in the product documentation
before using the equipment.
Keep manual for future reference.
The Waste Electrical and Electronic Equipment Regulations indicate separate collection for
electrical and electronic equipment.
○ Power Off.
ㅣ Power On
Manufacturer
Date of manufacture
Serial Number
This equipment generates, uses, and can radiate radio frequency energy and, if not installed and used in
accordance with the instructions, may cause harmful interference to other devices in the vicinity. If
installed correctly, there is still no guarantee that interference will not occur in a particular installation.
If this equipment does cause harmful interference to other devices, which can be determined by turning
the equipment on and off, user is encouraged to try correcting the interference by one or more of the
following measures.
Classification
1) Class I equipment
2) Ordinary equipment
3) Equipment not suitable for use in the presence of a flammable anesthetic mixture containing air,
oxygen, or nitrous oxide.
4) Continuous operation
Accessory equipment connected to the analog and digital interfaces must be certified according to the
respective IEC standards (i.e. IEC 60950 for data processing equipment and IEC 60601-1 for medical
equipment).
Furthermore, all configurations must comply with the system standard IEC 60601-1-1.
Anyone connecting additional equipment to the signal input or output part is configuring a medical
system, and is therefore responsible to ensure the system complies with the requirements of IEC
60601-1-1. If in doubt, consult a technical services department or your local representative.
Any changes or modifications not expressly approved by the manufacturer could void the
user’s authority to operate the equipment.
The RSM 2430C / RSM 2430C Choice detector and associated cables must not be operated
in the presence of moisture.
To avoid excessive product leakage currents and maintain product compliance to medical
protective grounding requirements, the Control Box’s power cord must be connected
directly to a hardwired AC Mains receptacle. Under no circumstances shall the Control
Box's power cord be connected to a multiple receptacle extension device that supplies power
to other electrical hardware which is electrically connected to the Control Box.
The RSM 2430C / RSM 2430C Choice detector is not suitable for operation in the presence
of a flammable anesthetic mixture containing air, oxygen, or nitrous oxide.
The RSM 2430C / RSM 2430C Choice is designed for use in Digital X-ray Images of
woman breast diagnosis. (mammography). We are confident you find it is superior to
radiographic film/screen systems in general-purpose diagnostic procedures. The system can
be applied wherever traditional X-ray screen-film cassettes are currently used.
Follow all safety labels on the equipment.
The operator must not touch part of the X-ray machine or electrical input, or patient
simultaneously.
Sealed System
The Detector Panel is sealed so that biological fluids will not penetrate the outer casing during normal
use. The exterior of the array can be cleaned with common hospital decontamination solutions,
including 20% chlorine bleach solution (1 part bleach to 4 parts water). A 5% gluteraldehyde or 70%
alcohol solution can also be used. To apply the cleaning solution, power down the system and
disconnect from the power source, moisten a cloth with the solution, and wipe the panel.
This equipment has been tested and found to comply with the limits for a Class A Digital Device,
pursuant to part 15 of the FCC Rules. These limits are designed to provide reasonable protection
against harmful interference when the equipment is operated in a commercial environment. This
equipment generates, uses, and can radiate radio frequency energy, and if not installed and used in
accordance with its Service Manual, may cause harmful interference to radio communications.
Operation of this equipment in a residential area is likely to cause harmful interference in which case
the user will be required to correct the interference at his/her own expense.
Any changes or modifications not expressly approved by the manufacturer could void the
user’s authority to operate the equipment.
The RSM 2430C / RSM 2430C Choice detector and associated cables must not be operated
in the presence of moisture.
To avoid excessive product leakage currents and to maintain product compliance to medical
protective grounding requirements, the Control Box’s power cord must be connected
directly to a hardwired AC Mains receptacle. Under no circumstances shall the Control
Box's power cord be connected to a multiple receptacle extension device that supplies power
to other electrical hardware, which is electrically connected to the Control Box.
The RSM 2430C / RSM 2430C Choice device provides a digital image capture capability
for conventional radiographic examinations (excluding fluoroscopy, angiography, and
mammography application). The system can be applied wherever traditional X-ray screen-
film cassettes are currently used.
Follow all instructions of safety labels on the equipment.
The operator must not touch part of the X-ray machine or electrical input, or patient
simultaneously.
Sealed System
The Detector Panel is sealed so that biological fluids will not penetrate the outer casing during normal
use. The exterior of the array can be cleaned with common hospital decontamination solutions,
including 20% chlorine bleach solution (1 part bleach to 4 parts water). A 5% glutaraldehyde or 70%
alcohol solution can also be used. To apply the cleaning solution, power down the system and
disconnect from the power source, moisten a cloth with the solution, and wipe the panel.
*Any area where patient moves (not only during imaging but also when entering and
leaving the room, etc.) is considered as part of the patient environment, therefore the
installation location should be determined upon consultation with the user regarding areas
outside of the patient environment.
*Example of a patient environment. (Arrows indicate minimum distance)
Figure 1. (A) Set-up for image processing, (B) Set-up for Image evaluation
RF emission
Class A
CISPR 11
The IEC61000-4-11
only applies to
SSU0213 System
Power Box.
Magnetic field in The magnetic field in
the source the source frequency
frequency should be equivalent to
30A/m 30A/m
(50/60Hz) those of general
commercial or hospital
IEC 61000-4-8 settings.
d = 2.33√p800MHz ~
2.5GHz,
where p is the
transmitter-receiver’s
maximum power rating
in watts (W) and d is the
recommended interval.
When the RSM 1824C is disturbed by EM, the obtained images could have an abnormal
condition such as artifacts or noise.
RSM 2430C / RSM 2430C Choice is designed for use in Digital X-ray Images of woman breast
diagnosis. We are confident that you will find it is superior to radiographic film/screen systems in
general purpose diagnostic procedures.
RSM 2430C / RSM 2430C Choice differs from traditional X-ray systems in that part. Instead of
exposing a film and chemically processing it to create a hard copy image, a device called Detector
Panel is used to capture the image in electronic form.
RSM 2430C / RSM 2430C Choice is a flat-panel digital X-ray detector that captures projection
radiographic images in digital format within seconds, eliminating the need for an entire X-ray film or
an image plate as image capture medium.
RSM 2430C / RSM 2430C Choice detector is a direct conversion device in the form of a square plate
in which the input X-ray photons are absorbed through an X-ray sensitive photo conductor. The energy
of the incoming photons excites electron-hole pairs to conduction and the valence band. The charges
released due to absorption of the X-rays are collected by the applied electrical potential across the
photo conductor. The charges are converted to a modulated electrical signal through thin film
transistors. The amplified signal is converted to a voltage signal again and is then converted from an
analog to digital signal which can be transmitted to a monitor for viewing or storing electronic data file,
for later viewing.
The API provided with RSM 2430C / RSM 2430C Choice detector allows to integrate the system with
the user interface software which supports digital imaging and communication in medicine (DICOM)
and Image Processing.
The RSM 2430C / RSM 2430C Choice should be operated and stored according to the specifications
of Table 1.
2.8 Warranty
RSM 2430C / RSM 2430C Choice Detector by DRTECH Corporation will honor a warranty of two
years from shipment date, as long as Detector is operated under normal conditions, as defined in Table
1. Optimal conditions of operation and storage [Recommend] are specified in section 2.7, Storage
Requirements.
In order to ensure detector’s safety from shock, environment temperature, and unproved disassembly,
‘Indicating sensors’ and ‘Warranty Sealing Tape’ are installed within RSM 2430C / RSM 2430C
Choice detectors as specified in section 3.4, Indicating sensors and Labels.
Do not ever put any object or press on the top of RSM 2430C / RSM 2430C Choice
detector giving strong pressure. Otherwise the detector panel may not operate or
unexpected images may appear improperly, and there might be a chance for detector to be
physical damaged.
DRTECH shall not be held liable for any problem caused by user negligence and is not
responsible for refunding the user in such case.
• Performance
Contents Unit Details
DQE % ≥ 50%@ 0.5lp/mm
MTF % ≥30% @ 5lp/mm (※ Truview ART)
Cycle time Sec ≤ 13 sec. (※ EWT 2.5s)
X-ray Window Sec ≤ 5 sec.
Preview Time Sec ≤ 4 sec. (※ EWT 2.5s)
Frame Rate - 1fps (Static mode)
Push Button to X-ray msec < 50
Data Output/Interface - Gigabit Ethernet
X-ray Generator Interface - AED mode
• Mechanical
Contents Unit Details
Chest Wall Distance mm ≤2.0
Lateral Wall Distance mm < 17.7
Overall Dimension mm 327.5±0.3mm(W) х 253.75±0.3mm (L) х 14.2±0.5mm (D)
Weight kg 1.2±5%
RSM 2430C / RSM 2430C Choice can support screening X-ray imaging in digital mammography
system.
In order to get the X-ray image by using RSM 2430C / RSM 2430C Choice, the detector should be
adapted to the system with signal interface by using ‘Gigabit Ethernet communication’. The
functionality of RSM 2430C / RSM 2430C Choice and Gigabit-Ethernet communication device are
shown in Table 3.
Do not put any object or press on the top of RSM 2430C / RSM 2430C Choice detector giving strong pressure. Otherwise the detector
panel may not operate or unexpected images may appear improperly, and there might be a chance for detector to be physical damaged.
DRTECH shall not be held liable for any problem caused by user negligence and is not responsible for refunding the user in such case.
Labels
The labels are two different types of RSM 2430C / RSM 2430C Choice detector of DRTECH
Corporation Product Rights and warranty sealing. Please do not peel off the labels. Any label peeled
or evidence of attempt to peel will void the warranty of product.
4.1.1 Connectors
Figure 9. Connectors
The products have Lower breaking capacity type. So do not install at the building
power system prospective short-circuit current exceeding 16 A or 35 A.
RSM 2430C / RSM 2430C Choice detector can communicated with ‘Gigabit Ethernet Interface’
through CAT6 Legacy commercial connector, with the LAN cable as shown in Figure 9. The image
data is transmitted by Ethernet port.
DC power is applied through a POE cable. In order to turn on the detector power, POE cable should
be connected as shown in Figure 10.
Clear instructions should be given to prevent EQUIPMENT from mispositioning, and device
disconnection should not be easily done.
The detector’s main power must be supplied by the OEM to meet applicable regulatory agency
requirements. When operating the Digital X-ray Detector, the detachable power supply adaptor
and cord shall be provided complying with the following regulations:
- Certified detachable power cord, Type SJT, min. No. 18 AWG rated min. 10A, 125V, 3-
conductor terminating in molded-on listed “Hospital Grade” attachment plug of grounding
type attachment plug with parallel blade, Maximum 4.0m long. Either 125V NEMA 5-15P or
250V NEMA 6-15P type must be used.
The API is a regular DLL using shared MFC DLLs and contains exported functions for image data
acquisition.
For detailed information, please refer to the API manual.
4.2.2 Calibration
The Detector Panel is shipped completion of calibration process, from the manufacturing site. Still, the
user may need to run additional calibration processes during installation. Calibration may be needed
regularly during normal use as well.
For detailed information, please refer to the GMP manual.
4.2.3 Warming up
In order to optimize system operation, the system should be warmed up for at least 10 minutes after
applying to the detector main power.
Minimum 5 min
Recommend 10 min
5.1 Unpacking
6 Software CD - 1 □
If you find any items missing from the list above upon unpacking, please contact DRTECH
Corporation.
The packaging that came with the product should not be damaged or discarded as it is
needed later for after-sales services or to exchange the product with a new product.
If the packaging or any component is missing, the damaged product cannot be refunded or
exchanged with a new product.
4. After installation, be sure to dispose waste product packaging with care and with full respect to the
environment.
DRTECH shall not be held liable for any problem caused by user negligence or any
incidents due to of instructions not being followed during installation.
1. Required pc Specifications
Items Minimum Recommended
CPU Intel i5-3470 Intel i7-4790
RAM 4 GB 8 GB
SSD 128 GB
HDD 500 GB
500 GB
NVIDIA GeForce NVIDIA GeForce
VGA
GT630 1 GB GT630 1 GB
ODD N/A DVD Recorder
Windows 7 Pro Windows 7 Pro
OS
32 / 64 bit 64 bit
Display Size 23 inches 27 inches
Display Resolution 1600 x 900 1920 x 1080
LAN Gbps Ethernet Card EXPI9301CTBLK
2. IP address setting
In order to connect the Gigabit Ethernet communication, you can setup the IP address as below:
“192.168.250.100” and subnet mask as “255.255.255.0”
4. Etc PC setting
Please refer to RCali1 User Manual for details.
Take a white field X-ray image (exposure conditions can be determined by user in the linear region,
not in saturated exposure region).
In both cases, perform the “Calibration Procedure” implemented in the UI software or in independent
image viewer software of DRTECH.
If the artifact is not eliminated by the Calibration Procedure, then contact DRTECH service.
Sensitivity: Take a white field (with 40 mm thickness Acryl plate, without any object on the top
of detector) X-ray image at the exposure conditions which have gray value of 2300~2500 pixel
counts. Check the exposure conditions by using dose-meter. Take ROI of 256 by 256 area,
approximately.
ACR Phantom: Take an ACR phantom with three different patterns of fibers, calcifications, and
masses. Numbers of Fibers, calcifications, and masses patterns are six, five, and five,
respectively. The RSM 2430C / RSM 2430C Choice can be shown in exposure condition of 28
kV, 80 mAs that has patterns of five, four, and four, respectively.
If there is any abnormality, then perform the “Calibration Procedure” provided by UI software
supplier or by the independent image viewer software of DRTECH.
Check to make sure temperature and humidity are good for normal operational rage.
RSM 2430C / RSM 2430C Choice requires at least 10 minutes to warm up after the main
power switch has been turned on.
Run the X-ray machine and acquire an image (Do not saturate the image with X-ray).
Check for any dead pixels (Dead lines or dead pixel points).
Check uniformity throughout IC blocks and the entire image.
Run setup program to install RCali1 software on a computer connected to RSM 2430C / RSM
2430C Choice detector.
Check configuration (Detector model, map file name etc.). Please refer to Instructions of RCali1
User Manual - Gain Calibration Procedure – from RCali1 User Manual.
When calibration procedure is over, a calibrated map file would be saved to the pre-defined folder
with file name specified in RCali1 configuration menu - Gain Calibration Procedure.
The RCali1 User Manual has been prepared for the appropriate use of the X-ray Detector Calibration
& Utility software developed by DRTECH Corporation. RCali1 User Manual provides the instructions
for the use of RCali1.
Information contained in this manual is confidential and is property of DRTECH Inc., which is only
provided to the authorized customers of DRTECH Inc. The purpose of the manual is to assist the users
to comprehensively utilize the product of DRTECH Inc. All information contained in the manual may
not be altered or distributed without prior written consent of DRTECH Inc., and may not be disclosed
to unauthorized personnel. Information contained in the manual may be altered without prior notice.
In order to initiate the claim process, please follow the steps indicated below.
2. Once we check your CDN and raw images, we will look into your case immediately.
3. Our Customer Service Team will remain comments or recommendation about the issue in CRM site,
They could ask online checking.
A. Please give us your feedback about our online support (telling us if the information was useful) in
a timely manner.
4. If the problem is not solved through on-line support or it is determined that the faulty product needs to
be returned after CDN submission, an RMA will be issued through CRM. After an RMA is issued, you
can return your faulty product in its original packing to DRTECH.
5. Our Customer Support Team will also check for the warranty status of the product.
6. The returned product will be packed in its original packing accompanied with the following markings
on the outer box: FRAGILE, HANDLE WITH CARE, UP, DOWN.
7. The repair turn-around time will take as less as two weeks, from the date of receipt of product.
8. After DRTECH receives the product, all out-of-warranty repairs will be accompanied with a service
quote (SQ) accordingly based on the predicted cost of the repair work - DRTECH will start the repair
work after getting your confirmation accompanied by a signature (sent by fax or e-mail) on the SQ
issued. The SQ, with your signature, is considered a purchasing order (PO). (The SQ number will be
used as the PO number)
9. All repairs of systems covered by warranty will be started in a timely manner by DRTECH. Please
understand that damage due to abuse or misuse by customers is not covered by warranty. A SQ will be
issued in such case.
Thank you