CareView 1500Cw Operation Manual

Distribution No.: Document Type: Document No.
Technical Files RD-OI-16
Title: CareView 1500Cw Operation Manual Total: 55 pages
Editor Auditor Approval
Revision History
Version Date Description Author
2015.01.19 Initial Release Leilei. Li
2015.03.02 Updated Leilei. Li
2015.03.10 Delete wireless AP and software information Leilei. Li

A/0
2015.03.24 Update the battery charger Leilei. Li
Added the content of RF and EMC according the
2015.06.24 Leilei. Li
FDA requirement.
2016.01.19 Update the product component Leilei. Li
X-ray Flat Panel Detectors
CareView 1500Cw
Operation Manual
Before using the instrument, be sure to read this manual thoroughly.

Also, read the manuals of other instruments in the system.
Keep the manual where it is easily accessible.
Page 1 of 55 RD-OI-16 A/0

Copyright Statement
Copyright by CareRay Digital Medical System Co., Ltd. All rights reserved.
No part of this document may be reproduced, translated, or transmitted without the
express written permission of CareRay Digital Medical System Co., Ltd.
CareRay reserves the right to change the specification, configuration and appearance of
the product without prior notice.
CareRay is not liable for errors or omissions contained in this manual or for any damages
incurred in connection with furnishing or use of this manual.
This manual is intended to help Original Equipment Manufacturers in the installation of
CareView 1500Cw and its first operation. It also provides information for service and
safety operation. The figures and data given in this manual can’t be considered to be a
contractual specification.
CareRay does not distribute the CareView 1500Cw to the end-users but only to OEM or
retrofitters who are responsible of the installation of the CareView 1500Cw into the
radiography system. The equipment manufacturer or retrofitter is also responsible of the
validation of the CareView 1500Cw performance for the foreseen application.
Please read this manual carefully before performing any installation or use of the
CareView 1500Cw. Consult CareRay for additional information.

General Safety Information
Follow the safety instructions in this manual and all the warnings printed on the warning
labels. Ignoring such cautions or warnings while handling the product may result in injury
or accident. Be sure to read and fully understand the manual before operating the X-ray
flat panel detectors to avoid any unnecessary damage and personal harmful.
Caution: Federal law (U.S.) restricts this device to sale by or on the order of a physician
or a licensed practitioner.
Warning: The users are responsible for the use and maintenance of the product. The
product must be used only by qualified personnel who are familiar with the operation of
electrical equipment.
Warning: X-ray imaging system, image processing, reading of image, and storage of data
must be performed in accordance with the law of the country where the product is used.
Also, the user is responsible for maintaining the privacy of image data.
Warning: This product may malfunction due to electromagnetic waves. Keep away from
the environment with strong electromagnetic field.
Warning: To avoid the risk of electric shock, this equipment must only be connected to
supply mains with protective earth.
Warning: The product must be connected to the appropriate power source which
recommended by CareRay to avoid unnecessary risks.
Warning: Use only the original power cords. Inspect power cords and connectors
regularly. Cord and connector repairs should only be serviced by qualified personnel.
Warning: The SIP/SOPs are for connection to certified IEC 60950-1 equipment only.
Warning: If any abnormal phenomenon is evident such as smoke, strange sound or fume,
immediately turn off the power of each instrument, unplug the power cable from the AC
outlet, and contact your dealer, distributor or CareRay. Further use may be dangerous.
Warning: In case of an accident or malfunction, unplug the power cable immediately and
contact your dealer, distributor or CareRay. Further use may cause fire, electrical shock or

other damage.
Warning: Install the X-ray flat panel detectors horizontally on a flat, stable surface. If the
detector is placed vertically or in any tilted position, the detector must be securely
fastened in position. The X-ray flat panel detectors may cause an injury if it falls or is
dropped.
Warning: Forbidden hand-held the detector during normal use.
Warning: No modification of this equipment is allowed.
Warning: Do not modify this equipment without authorization of the MANUFATURER.
Warning: If this equipment is modified, appropriate inspection and testing must be
conducted to ensure continued safe use of the equipment.
Warning: Disposal of this product in an unlawful manner may have a negative impact on
health and on the environment. When disposing of this product, therefore, be absolutely
sure to follow the procedure which is in conformity with the laws and regulations
applicable in your area.
Battery Pack and Battery Charger Safety Information
Warning: Be sure to use only the dedicated battery pack for the CareView 1500Cw
detector.
Warning: The product configures a plug-in battery. Forbid modify or change the inner
battery by yourself, otherwise damage the device, even cause short circuit or fire.
Warning: The change of Li-polymer battery must be operated by a qualified engineer.
Warning: Use the dedicated battery charger. Otherwise, a battery explosion or a battery
leak may occur, resulting in fire or electrical shock.
Warning: Do not let the battery pack and battery charger come into contact with water or
other liquids and do not allow them to get wet.
Warning: Remove the battery out of the detector if the device is not likely to be used for
some time.
Note: The battery charger for X-ray detectors hereafter referred to as battery charger.

Pediatric Application
Caution: Use of equipment and exposure settings designed for adults of average size
can result in excessive radiation exposure for a smaller patient. Studies have shown that
pediatric patients may be more radiosensitive than adults (i.e., the cancer risk per unit
dose of ionizing radiation is higher), and so unnecessary radiation exposure is of
particular concern for pediatric patients.
Warning: Every request should be reviewed by the pediatric radiologist prior to beginning
the examination to insure correct study is being performed.
Warning: The technologist should use the proper technique for the patient’s size to
decrease the radiation dose when the technologist acquires diagnostic images.

Regulatory Requirements
Equipment Standards
IEC/ES 60601-1 Medical Electrical Equipment
CAN/CSA-C22.2 No. General Requirements for Basic Safety and Essential

60601-1 Performance
IEC/EN 60601-1-2 Medical electrical equipment

Part 2: Electromagnetic Compatibility–Requirements and Tests
IEEE 802.11a/b/g/n Wireless Communications
Radio Frequency (RF) compliance information

USA FCC Part 15 Subpart B Class B and Part 15 Subpart C
European Union EN 300328 V1.8.1

EN 301489-1 V1.9.2
EN 301489-17 V2.2.1
EN 301893 V1.7.1
EN 50566:2013
EN 62209-2:2010

FCC Rules
This device complies with Part 15 of the FCC Rules. Operation is subject to the following
two conditions:
(1) This device may not cause harmful interference.
(2) This device must accept any interference received, including interference that may
cause undesired operation.
Note: 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 the instruction 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 own expense.
Caution:
(1) For operation within 5.15~5.25GHz frequency range, it is restricted to indoor
environment.
(2) Any changes or modifications (including the antennas) made to this device that are
not expressly approved by the manufacture may void the user’s authority to operate
the equipment.

Guidance and Manufacturer’s Declaration for
EMC Directive
This device has been tested for EMI/EMC compliance, but interference can still occur in
an electromagnetically noisy location. Attempt to maintain a suitable distance between
electrical devices to prevent malfunction.
Electromagnetic Emissions
The CareView 1500Cw detector is intended for use in the electromagnetic environment
specified below.
The user of the CareView 1500Cw detector should assure that it is used in such an
environment.
Immunity Test Compliance Electromagnetic Environment – Guidance
The CareView 1500Cw detector uses RF energy
RF Emissions only for its internal function. Therefore, its RF
Group 1 emissions are very low and are not likely to
CISPR 11 cause any interference in nearby electronic
equipment.
RF Emissions The CareView 1500Cw detector is suitable for
Class A
CISPR 11 use in all establishments other than domestic
Harmonic emissions and those directly connected to the public

Class A
IEC 61000-3-2 low-voltage power supply network that supplies
Voltage fluctuations/ buildings used for domestic purposes.
flicker emissions Complies
IEC 61000-3-3
Electromagnetic Immunity
The CareView 1500Cw detector is intended for use in the electromagnetic environment
specified below.
The user of the CareView 1500Cw detector should assure that it is used in such an
environment.

IEC 60601 Compliance Electromagnetic Environment –
Immunity Test
Test Level Level Guidance
Floors should be wood, concrete or
Electrostatic
±6㎸ contact ±6㎸ contact ceramic tile. If floors are covered
discharge (ESD)
±8㎸ air ±8㎸ air with synthetic material, the relative
IEC 61000-4-2
humidity should be at least 30%.
±2㎸ for ±2㎸ for
Electrical fast power supply power supply Mains power quality should be that
lines lines
transient/burst of a typical commercial or hospital
IEC 61000-4-4 ± 1 ㎸ for ± 1 ㎸ for environment.

input/output input/output
lines lines
±1㎸ ±1㎸
differential differential Mains power quality should be that

Surge mode mode
of a typical commercial or hospital
IEC 61000-4-5
±2 ㎸ ±2 ㎸ environment.
common common
mode mode
<5% Uт <5% Uт
Mains power quality should be that
(>95% dip in (>95% dip in
Voltage dips, Uт) for 0.5 Uт) for 0.5 of a typical commercial or hospital
cycle. cycle.
short environment. If the user of the
40% Uт 40% Uт
interruptions and CareView 1500Cw detector image
(60% dip in (60% dip in
voltage Uт) for 5 Uт) for 5 intensifier requires continued
cycles. cycles.
variations on operation during power mains
70% Uт 70% Uт
power supply interruptions, it is recommended
(30% dip in (30% dip in
input lines Uт) for 25 Uт) for 25 that the CareView 1500Cw detector
cycles. cycles.
IEC 61000-4-11 image intensifier be powered from
<5% Uт <5% Uт
an uninterruptible power supply or a
(<95% dip in (<95% dip in

Uт) for 5 sec. Uт) for 5 sec. battery.
Power frequency Power frequency magnetic fields
(50/60 ㎐) should be at levels characteristic of

3 A/m 3 A/m
magnetic field a typical location in a typical
IEC 61000-4-8 commercial or hospital environment.
NOTE: Uт is the a.c. mains voltage prior to application of the test level.
IEC 60601 Compliance Electromagnetic Environment –

Immunity Test
Test Level Level Guidance
Portable and mobile RF
communications equipment should be
used no closer to any part of the
CareView 1500Cw detector, including
cables, than the recommended
separation distance calculated from the
equation applicable to the frequency of
3 Vrms the transmitter.
Conducted RF
150 kHz to 80 3 Vrms Recommended separations distance
IEC 61000-4-6
MHz d=1.2√𝑃
Recommended separations distance

d=1.2√𝑃 80 MHz to 800 MHz
d=2.3√𝑃 800 MHz to 2.5 GHz
where P is the maximum output power

rating of the transmitter in watts (W)
according to the transmitter
3 V/m manufacturer and d is the
Radiated RF
80 MHz to 2.5 3 V/m recommended separation distance in
IEC 61000-4-3
GHz metres (m).
Field strengths from fixed RF

transmitters, as determined by an
electromagnetic site survey a, should
be less than the compliance level in
each frequency range b.
Interference may occur in the vicinity of

equipment marked with the following
symbol:
NOTE 1: At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is
affected by absorption and reflections from structures, object and people.

a
Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless)
telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV
broadcast can-not be predicted theoretically with accuracy. To assess the
electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey
should be considered. If the measured field strength in the location where the CareView
1500Cw detector is used exceeds the applicable RF compliance level above, the
CareView 1500Cw detector should be observed to verify normal operation. If abnormal
performance is observed, additional measures may be necessary, such as reorienting or
relocating the CareView 1500Cw detector.

b
Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
Recommended Separation Distances
The CareView 1500Cw detector is intended for use in an electromagnetic environment in
which radiated RF disturbances are controlled. The user of the CareView 1500Cw
detector can help prevent electromagnetic interference by maintaining a minimum
distance between portable and mobile RF communications equipment (transmitters) and
the CareView 1500Cw detector as recommended below, according to the maximum
output power of the communications equipment.

Rated maximum Separation distance according to frequency of transmitter
output power of m
transmitter 150kHz~80MHz 80MHz~800MHz 800MHz~2.5GHz
W d=1.2√𝑃 d=1.2√𝑃 d=2.3√𝑃
0.01 0.12 0.12 0.23

0.1 0.38 0.38 0.73
1 1.2 1.2 2.3
10 3.8 3.8 7.3
100 12 12 23
For transmitters rated at a maximum output power not listed above, the recommended
separation distance d in meters (m) can be estimated using the equation applicable to the
frequency of the transmitter, where P is the maximum output power rating of the
transmitter in watts (W) according to the transmitter manufacturer.
NOTE 1: t 80 MHz and 800 MHz, the separation distance for the higher frequency range
applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is
affected by absorption and reflection from structures, objects and people.

Glossary
Abbreviation Description
OEM Original equipment manufacturer
SIP/SOP Signal input/output part
XFPD X-ray flat panel detector
API Application program interface
DR Digital radiography
DROC Digital radiography operator controller
F2AED Full-Field automatic exposure detection
TFT/PD Thin-film transistor/ Photo-diode
DQE Detective quantum efficiency
LED Light emitting diode
LAN Local area network
SID X-ray source to detector Distance
Fps Frame per second
lp/mm Line pair/mm
TBC To be confirmed
FTP File transfer protocol
STP Shielded twisted pair
AP Access point

Symbols
Symbol Description Symbol Description
Manufacture date Caution
Handle with care Manufacturer
Don’t roll This way up
Stacking limit by
Keep dry
number
Authorized
Keep away from
representative in the
sunlight
European Community
ESD warning CE mark
Operating instructions UL mark
Direct current Disposal (WEEE)
Warning: dangerous
Serial number
voltage
Type B applied part Handle gently
Refer to instruction
Non-ionizing radiation
manual/booklet
Protective earth
CareRay logo
(ground)

Contents
Copyright Statement………………………………….…………………………………….2
General Safety Information……………………….………………………………….........3
Regulatory Requirements……………………….…………………………………………6
FCC Rules………………..……………………….…………………………………………5
Guidance and Manufacturer’s Declaration for EMC Directive……………….………...8
Glossary…………………………………………………………………………………… 13
Symbol ………………..……………………..……..…………….……………………...…14
1 Overview....................................................................................................................18
1.1 Principle...............................................................................................................18
1.2 Features ..............................................................................................................18
1.3 Product Classification .........................................................................................19
1.4 Intended Use .......................................................................................................19
1.5 Product Components ..........................................................................................19
2 Detector .....................................................................................................................20
2.1 Detector Description ...........................................................................................20
2.2 Detector Specifications .......................................................................................22
2.3 Typical Patient Doses .........................................................................................23
2.4 Detector Dimension.............................................................................................24
3 Battery Charger and Battery Pack ..........................................................................24
3.1 Battery Charger Component ...............................................................................24
3.2 Charging Dock Description .................................................................................24
3.3 Battery Charger Specifications ...........................................................................25
3.4 Li-Polymer Battery Specifications .......................................................................26
3.5 Li-Polymer Battery Dimension ............................................................................27
3.6 Charging Method.................................................................................................27
4 Power Box .................................................................................................................28
4.1 Power Box Description........................................................................................28
4.2 Power Box Specification .....................................................................................29
4.3 Power Box Dimension.........................................................................................30
4.4 Fuse ....................................................................................................................30
4.5 Operation.............................................................................................................31
5 Wireless Communication ........................................................................................31
5.1 Architecture .........................................................................................................32
5.2 Specification ........................................................................................................32

5.3 Initial Setting Value..............................................................................................33
5.4 Wireless LAN Diagnostics...................................................................................34
5.5 Intended Use Environment .................................................................................34
6 System Integration ...................................................................................................35
6.1 System components ...........................................................................................35
6.1.1 Recommended Generator Specification .........................................................35
6.1.2 Detector Operation Conditions ........................................................................35
6.1.3 Workstation and Software ...............................................................................36
6.2 DR System Connection .......................................................................................37
6.2.1 Wireless Connection using Wireless AP – Way1 ............................................37
6.2.2 Wireless Connection using Wireless AP – Way2 ............................................38
6.2.3 Wired Connection ............................................................................................38
6.3 X-ray Exposure Mode .........................................................................................38
6.3.1 Soft Sync Mode ...............................................................................................39
6.3.2 Manual Sync Mode..........................................................................................39
6.3.3 Auto Sync Mode ..............................................................................................40
7 Packing and Contents..............................................................................................41
8 Installation.................................................................................................................42
8.1 Hardware Installation ..........................................................................................42
8.2 Network Configuration ........................................................................................44
8.3 Turn off the device .............................................................................................47
9 Announcement .........................................................................................................48
9.1 Basic Notices ......................................................................................................48
9.1.1 Operation Conditions.......................................................................................48
9.1.2 Use-method of Power Supply .........................................................................48
9.1.3 Network ...........................................................................................................48
9.1.4 Electromagnetic Radiation ..............................................................................49
9.1.5 Contraindication...............................................................................................49
9.2 Particular Notices ................................................................................................49
9.2.1 Personnel ........................................................................................................49
9.2.2 X-ray Scope .....................................................................................................49
9.2.3 Operation Conditions.......................................................................................50
10 Maintenance ..............................................................................................................50
10.1 Inspections ..........................................................................................................50
10.2 Maintenance........................................................................................................51
10.3 Cleaning ..............................................................................................................51

10.4 Maintenance Note ...............................................................................................52
11 Storage and Transportation ....................................................................................52
11.1 Storage ................................................................................................................52
11.2 Transportation .....................................................................................................53
12 Emergency ................................................................................................................53
13 Disposal.....................................................................................................................53
14 Appendix A................................................................................................................54

1 Overview
1.1 Principle
CareView 1500Cw is a kind of wireless portable digital X-ray flat panel detectors which
have 434mm×355mm imaging area. The device communicates by not only the wireless
communication but also wired communication feature (Giga-bit Ethernet communication
mode by connecting the power box) optionally.
The device intercepts X-ray photons and then the scintillator emits visible spectrum
photons that illuminate an array of photo detectors (a-Si) that create electrical signals.
After the electrical signals are generated, it is converted to a digital value and an image
will be displayed on the monitor.
The detector should be integrated with an operating PC and an X-ray generator to utilize
as digitalizing X-ray images and transfer for radiography diagnostic.
1.2 Features
 Wireless communication (IEEE 802.11a/b/g/n) feature, and support double frequency
(2.4GHz/5GHz).
 14"x17" cassette-size detector easily fits into standard bucky tray cabinets for old
system upgrade, while CareView 1500Cw is also a good choice for general
radiography imaging systems.
 Designed with simple wiring and lightweight for portable applications.
 No connection to generator is necessary due to patented Full-Field Automatic
Exposure Detection (F2AED) Technology.
 High capacity battery and low-power operation ensure hundreds of X-ray shots in a
single-charge.

 Light weight and slim design, built-in foldable handle, rubber insulated frame and high
strength aluminum-alloy case ensure safe and convenient moves, and also improve
image quality under vibrating environment.
1.3 Product Classification
Table 1 Classification
Item Classification
Type of protection against Class I equipment

electric shock Internally powered
Degree of protection against
Type B applied part
electric shock
Mode of operation Continuous operation
NOT suitable for use in the presence of a flammable
Flammable anesthetics anesthetic mixture with air or with oxygen or nitrous
oxide.
1.4 Intended Use
The CareView 1500Cw detector is indicated for digital imaging solution designed for
providing general radiographic diagnosis of human anatomy. It is intended to replace
radiographic film/screen systems in all general-purpose diagnostic procedures. This
product is not intended for mammography applications.
1.5 Product Components
X-ray Imaging system consists of CareView 1500w detector, battery charger, battery pack
and accessories.
Table 2 Product components

Item Description Quantity
Detector Model: CareView 1500Cw 1
Li-Polymer battery
Model: 4ICP/83/3/103 1
(not connected)
Battery charger Model: CBC-ICP3A 1

Software API(for system integration manufacturer) 1
AC Power cable / 1
Supply electrical power to the detector while
Power box 1
communicating wired
Connected with detector and power box
Interface cable 1
7 meters
Note: The AC power cable must follow the requirements of the country where the product
is used. Besides, UL-approved power cable shall be used.
2 Detector
2.1 Detector Description
The front view and back view of CareView 1500Cw detector is shown in figure 1 and
figure 2. The detailed descriptions are shown in table 3.
Figure 1 Front view of CareView 1500Cw
③
④

Figure 2 Back view of CareView 1500Cw
Table 3 Description of detector
No. Name Description

Low density, low X-ray absorption and high intensity
○
1 Carbon fiber plate
protection layer
○
2 Built-in foldable handle Hold this handle when carrying the detector
Supply electrical power to the detector while

○
3 Battery pack
communicating wirelessly
○
4 Wifi antenna Transmits data with wireless communications
○
5 Detector label Display the information of detector
Note: Make sure the built-in foldable handle fixed well to avoid opened itself or dropped
by the shocking, when using the CareView 1500Cw fixed into the bucky.
The side view of CareView 1500Cw is shown in figure 3. The detailed descriptions are
shown in table 4.
⑩
⑦ ⑧ ⑨
⑥ Figure 3 Side view of CareView 1500Cw
Table 4 Description of side view
○
6 Power button Press to power on or off the detector
○
7 Power LED (Green) Indicates power on/off status.
ON: 802.3 cable mode
○
8 Network LED (Blue) Blink: 802.11 WIFI mode
OFF: No network connection
ON: Battery charging

○
9 Charging LED (Orange) Blink: Battery discharging, but electricity isn’t
enough

OFF: Charged complete
Allow the detector to communicate with Power
○
10 I/O interface
box via Interface cable
2.2 Detector Specifications
Table 5 Detector specification
Item Description
Model CareView 1500Cw

Purpose General radiography
Image matrix size 2304 × 2816 pixels
Pixel pitch 154 μm
Effective imaging area 355 mm × 434 mm
Grayscale 16 bit, 65536 grayscale
Scintillator CsI (Cesium Iodide)
Fill factor 0.65
Spatial resolution Min. 3.3 line pair/mm
Dynamic range ~82 dB
~70%..........(@ 1lp/mm)
MTF ~40%..........(@ 2lp/mm)
~22%..........(@ 3lp/mm)
(@RQA5, 30μGy)
DQE ~65%..........(@ 0lp/mm)
~20%..........(@ 3lp/mm)
Rated Power Supply DC 24 V, Max.1.5 A
 Wireless  Powered by the battery pack
 Wired  Powered by the power box using interface
cable
Power Consumption Max. 36 W
Wireless Communications IEEE 802.11a/b/g/n (2.4 GHz / 5 GHz)
Imaging plate Carbon fiber plate
Cooling Air cooling
Dimensions (L × W × D) 460mm × 384mm × 15mm
Weight (including battery pack) 3.7Kg
Environmental Requirements
Temperature: 5 ~ +35℃
Operation
Humidity: 30 ~ 75% (Non-Condensing)

Atmospheric pressure: 700 ~ 1060 hPa
Altitude: Max.3000 meters
Temperature: -20 ~ +55℃
Humidity: 10 ~ 90% (Non-Condensing)
Storage and transportation
Atmospheric pressure: 700 ~ 1060 hPa
Altitude: Max. 3000 meters
2.3 Typical Patient Doses
Typical patient dose is shown in below table which only serves as a reference. Real
dose will be a little different in practical condition.
Table 6 Typical patient doses

Body part Average adult patient size Dose (μGy)
Chest, PA 176
L-spine, AP 1770
Pelvis, AP Height: 170cm 910
Hand, AP Weight: 65kg 38
Knee, AP 150
Foot, AP 38
Note:
 PA is short for postero-anterior position, and AP is short for antero-posterior
position.
 Above dose is only for average-size adult patient.

2.4 Detector Dimension
Unit: mm
Figure 4 Detector dimension
3 Battery Charger and Battery Pack
3.1 Battery Charger Component
Table 7 Battery charger component
Item Description Quantity
Charging dock / 1
Switching power supply Model: HPU101-108 1
AC Power cable Optional 1
Note: UL-approved power cable shall be used.
3.2 Charging Dock Description
The structure of charging dock is shown in figure 5. The detailed descriptions are shown
in table 8.

Figure 5 Charging dock
Table 8 Description of charging dock

Connect the switching power supply to supply
○
1 DC Input
electrical power to the battery.
○
2 Battery Compartment Insert the battery pack to charge.
Indicates the power on/off status.

○
3 Power Indicator
(Green: Power on)
Indicates the charging status.
○
4 Charging Indicator
(Blue: Charging, Green: Fully Charged)
3.3 Battery Charger Specifications
Table 9 Battery charger specifications
Item Description
Model CBC-ICP3A
Simultaneous Charging Li-Polymer 3260mAh*3BAT
Charging Time 3.5 hours
Input AC 100-240V, 50-60Hz, Max.1.2A

Output DC 24V, Max. 4.16A
Total power for three battery 50.4W

Temperature: 5~35℃
Humidity: 30~75%RH
Operation
Atmospheric pressure: 700~1060 hPa
Temperature: -20~55℃
Humidity: 10~90%RH
Storage and transportation
Dimensions (L×W×D) 150.0mm × 128.0mm × 44.5mm
Net Weight Approx. 0.8Kg
3.4 Li-Polymer Battery Specifications
Table 10 Li-Polymer battery specifications
Item Description
Model 4ICP/83/3/103
Battery capacity 3260 mAh
Standard Voltage 14.8 V
Charging Voltage 16.8 V
Weight Approx. 320g
Environmental requirements
Temperature: 5~35 ℃
Operation
Humidity: 30~75 %RH
Temperature: -20~45 ℃
Storage (≤3 month)
Humidity: 15%~95 %RH
Temperature: 22~28℃
Storage (≥3 month)
Humidity: 15~95 %RH

3.5 Li-Polymer Battery Dimension
Unit: mm
Figure 6 Battery dimension
3.6 Charging Method
The battery pack supplies power to the detector during wireless connection. Be sure to
use only the dedicated battery pack and fully charge it before use.
1 Connect the power cable (switching power supply) to the DC input port of the
charging dock and the power cord to the power source to supply power. The power
LED lights in green indicating the presence of direct current (DC) power.
2 Insert the battery pack into the charging dock. Charging starts automatically. The
charge LED lights blue when the battery pack is being charged. After the battery pack
is charged completely, the charge LED lights in green.
3 Gently pull the charged battery pack to remove from the charging dock.
Warning: Be sure to stop charging the battery pack when the charge LED lights in green
beyond the specified charging time. Not doing so may result in battery pack overheating
or smoking or in explosion or fire.
Note: It takes approximately 3.5 hours to fully charge a battery pack. The required
charging time may vary depending on the temperature and remaining battery level.

4 Power Box
4.1 Power Box Description
Depending on the operating environment, the power box and using interface cable
enables the detector to be used through expansion to a wired connection.
The ports of power box are shown in figure 7. The detailed descriptions are shown in table
10.
○
4 ○
5 ○
6
○
1 ○
2 ○
3 ○
7 ○
8
Figure 7 Power box
Table 11 Description of power box
○
1 AC power inlet Input, 100~240V, 50/60Hz

○
2 Fuse case F2.5AL250V
○
3 Power Switch Turn on or off the power box
○
4 Port DC +24V output
Provides connection to the X-ray generator

○
5 Sync
(CareView 1500Cw doesn’t applicable)
Provides Gigabit Ethernet communication between the
○
6 LAN
workstation and detector
○
7 Rubber pad Provides a rough soft surface for the bottom side
○
8 Power box label Display the information of power box
4.2 Power Box Specification
Table 12 Power box specifications
Item Description
Supplying power to the detector when wired
Purpose
connection in the Digital Radiography
Input AC 100V~240V, 50/60 Hz
Output DC 24 V, Max. 4.2 A
Weight Approx. 620g
Environmental requirements
Temperature: 5~35 ℃
Operation
Humidity: 30~75 %RH (no condensation)
Temperature: -20~+55 ℃
Storage and transportation Humidity: 10~90 %RH (no condensation)

4.3 Power Box Dimension
Unit: mm
Figure 8 Power box dimension
4.4 Fuse
Two fuses are installed inside of power box to prevent electrical accidents due to an error
such as over current occurred in the AC Input. Stop immediately using power box when
fuses break.
Table 13 Fuse specification
Item Description
Model S501-2.5A
Amp Rating 2.5A
Voltage Rating 250V
Replacing Fuses
Note: Turn off the power box and pull the plug out of the power socket before replacing
fuses. And it must be replaced by a qualified engineer only.
Both CareRay and the users can replace it if necessary. The method is as follows:
1. Confirm the location of the fuse, which lies in the fuse holder with the symbol:

F2.5AL250V;
2. Pull the fuse holder out from its receptacle;
3. Take out the fuse from the fuse holder;
4. Check the fuses and replace it if necessary, using the fuse model and rating specified
above;
5. Push the fuse holder back and make sure it is installed well.
4.5 Operation
 Turn on the power

1 Connect the cables of equipment
Connect the AC power cable after connecting the interface cable and other cables,
and make sure all the cables connected properly and firmly.
2 Turn ON the power of the power box
Press the ‘I’ side of the power switch on the power box.
 Turn off the power

Note: Do not turn OFF the power of the control computer while the system is shutting
down. This may cause the product to malfunction or fail and/or data to be destroyed.
1 Turn OFF the power of the power box
Press the ‘O’ side of the power switch on the power box.
2 Turn OFF the power of the other equipment
If other equipment is connected, turn OFF its power.
5 Wireless Communication
The CareView 1500Cw includes two internal wifi antennas. The design of the system
should guarantee that the antenna is not electro-magnetically shielded when the detector
is placed inside a bucky.

5.1 Architecture
Figure 9 Architecture with wifi connection
5.2 Specification
Table 14 Wireless specification

Item Description
IEEE802.11 a/b/g/n
Wireless standard b/g/n for 2.4 GHz band
a/n for 5GHz band
For 2.4GHz Band
802.11b/g/n(20MHz):2412~2472MHz
802.11n(40MHz):2422~2462MHz
Frequency Range For 5.0GHz Band
802.11a/n(20MHz):5180~5220MHz,
5260~5320MHz,5500~5700MHz;
802.11n(40MHz):5190~5310MHz, 5510~5670MHz
2.4GHz:
13 for 802.11b/g, 802.11n (HT20)
Channel Number
9 for 802.11n (HT40)
5GHz:

19 for 802.11a, 802.11n (HT20)
9 for 802.11n (HT40)
Date Rate 802.11b: Max. 11Mbps
802.11a/g: Max. 54Mbps
802.11n: Max. 300Mbps (MIMO 2X2)
802.11b: DSSS (DBPSK, DQPSK, CCK)
Modulation
802.11a/g/n: OFDM (BPSK, QPSK, 16-QAM, 64-QAM)
Output power Max. 17dBm
Security 64/128-bits WEP, WPA, WPA2, 802.1x
Antenna Two Dual Band Antennas (Detector: Internal)
Antenna Gain 3dBi
5.3 Initial Setting Value
Table 15 Initial setting values of detector

Item Description
IP address 192.168.68.1
Subnet mask 255.255.255.0
CountryCode CN
1500Cwxxxx-5G
ESSID
(xxxx stands for four-bit number)
NetworkType Infrastructure
WirelessMode 11(N only with 5GHz band)
BandWidth 40MHz
Channel 149
AuthMode WPA2PSK
EncrypType AES
WPAPSK(Password) abcdefghij
The selection and configuration of the wireless AP see “Wireless Configuration and AP
Selection user guide” for detail.
Note:
1) The value of ESSID/ WPAPSK of the detector and wireless AP should be same, and
avoid overlapping with other systems for preventing confusion.
2) The wifi band and channel should comply with the local regulation. It has been in
several cases that wifi quality is better in the 5GHz band compared to the 2.4GHz
band. If possible and allowed in the local country, CareRay recommends the use of

the 5GHz band.
3) If wifi is used, it is mandatory to declare the country.
5.4 Wireless LAN Diagnostics
Table 16 Wireless WLAN diagnostics

Item Description
 Interface cable: Displays a wired connection status through interface
Interface cable
 Wireless: Display a wireless connection status
 The signal level of a wireless connection
 Displays 4 levels (max.4/ min.1), and if a warning sign is showed on
Quality
viewer at the 1st level where communication is not stable, check the
user environment.
Note:
(1) In case an acquired image would not be transmitted because of wifi link failure, there
is a possibility to recover the image later.
(2) In case of transmission failure, the last acquired image must be retrieved before any
other action.
(3) In case of the wifi communication is no more available; the wired connection should
be used for the last image recovering.
5.5 Intended Use Environment
As far as possible, keep the product away (1 - 2m) from electrical devices that generate
RF noise like microwaves, monitors, electric motors and etc.
Try to keep the antennas at least 15cm away from the wall or other objects. WiFi quality
may also depend on access point position and antenna orientations

6 System Integration
6.1 System components
The Digital Radiography (DR) system mainly contains three components.
 X-ray generator, tube and subsidiary equipment
 DROC (Digital Radiography Operator Controller) image workstation and software
 CareView 1500Cw detector and subsidiary equipment
6.1.1 Recommended Generator Specification

 Energy range: 40~150kVp
 mA range: 10~1000mA (depending on the generator power)
 ms range: 10~6300ms to produce 0.1~1000mAs (depending on the generator power)
Note: To our best knowledge, the detector is compatible with the X-ray generators with
the specifications described above. If you have questions regarding the compatibility
issue for other generators, please contact your distributor or CareRay.
6.1.2 Detector Operation Conditions

 X-ray energy range
The detector operates for the following X-ray tube peak voltages:
 X-ray tube peak voltages: Min = 40 kVp
 X-ray tube peak voltages: Typ = 70 kVp
 X-ray tube peak voltages: Max = 150 kVp
 X-ray exposure range
The detector operates within the linearity specifications up to the X-ray exposure
value of 100μGy.
The detector operates within the degraded linearity specifications above 100μGy and
up to the X-ray exposure value of 130 μGy.
 X-ray source position
The angle between the X-ray central propagation axis and the normal axis of the

front-end entrance plane taken at the centre point of the matrix - should remain within
the range:
 X-ray angle: Min = -45 deg
 X-ray angle: Typ = 0 deg
 X-ray angle: Max = +45 deg
The distance between the X-ray source focal spot and the front-end entrance plane
(SID) should remain within the range:
 SID: Min = 100 cm
 SID: Typ = 135 cm
 SID: Max = 180 cm
 X-ray window duration
Despite the X-ray window duration can be functionally settled by the system over a
wide range, the image quality can be directly impacted by the X-ray window duration
(leakage, noise, lag).
The full performance of the detector is guaranteed for the following X-ray window
range:
 X-ray window duration: Min = 10 ms (TBC)
 X-ray window duration: Typ = 500 ms (TBC)
 X-ray window duration: Max = 2500 ms (TBC)
6.1.3 Workstation and Software

Table 17 Workstation and software
Item Description
Operating system Windows XP/Win7
CPU Intel (R) Core (TM) 2 Duo, 2.93GHz or above
RAM 2 GB or higher
Hard Disk 160 GB or higher
Monitor 1280 x 1024 or higher

CD-ROM CD or DVD R/W
Development environment MS Visual Studio 2005
6.2 DR System Connection
CareView 1500Cw and DR station communicate (both for data and control) either
wireless by using a Wifi protocol or with a physical link by using a backup cable.
6.2.1 Wireless Connection using Wireless AP – Way1

Wireless AP should be selected and configured by user. Refer “Wireless configuration and
AP selection user guide” for detail.
The value of ESSID of the detector and wireless AP should be same. And avoid
overlapping with other system for preventing confusion.
The default IP address of detector is configured at 192.168.68.1, wireless AP’s IP address
is 192.168.68.10, DROC Station’s IP address is 192.168.68.100.
This typical connection is showed as below, and this is our recommended network
connection way. It can be applied in mobile DR, RAD DR, refined DR system.
Network Cable
IEEE 802.11n
Wireless AP
DROC Workstation CareView 1500Cw

Shielded X-ray Room
Figure 10 Wireless connection using Wireless AP (Powered by battery pack)
Note: If X-ray generator is installed in shielded X-ray room, it is recommended that
wireless AP also placed in it. Because the shielded X-ray room may be shield the wireless
signal. DROC Station connects with wireless AP through CAT-6 network cable that will
make sure good wireless network performance.

6.2.2 Wireless Connection using Wireless AP – Way2
The second method is the same as the first connection mode except the power mode. In
this mode, the detector is powered by power box.
Interface Cable
Power Box
Network Cable
IEEE 802.11n
Wireless AP AC 100-240V

Shielded X-ray Room
Figure 11 Wireless connection using Wireless AP (Powered by power box)
6.2.3 Wired Connection

When detector is powered by power box (not included), connect the CareView 1500Cw
with power box by interface cable, and then connect power box with DROC workstation
directly using Cat5e/Cat6 network cable. See figure 11 for detail.
Note: When detector is powered by power box, it must install in the buck.
Power Box Interface Cable
Network Cable
AC 100-240V
Figure 12 Wired connection (Powered by power box)
6.3 X-ray Exposure Mode
The synchronous connection mode is the signal transfer mode between the X-ray
generator which sends the X-ray and the detector which receives the X-ray. The sync
mode of CareRay’s static detector contains external sync, soft sync, manual sync and

auto sync.
CareView 1500Cw supported typical sync mode contains soft sync, manual sync and auto
sync containing FFAED mode.
Note: The detector can’t provide feedback to the generator to terminate the x-ray
exposure.
6.3.1 Soft Sync Mode

The detector communicates with X-ray generator by the DROC workstation and sync box
by a wired or wireless network connection. Compared with the external sync mode, the
soft sync mode will cause a delayed response.
The typical soft sync mode of DR system integrated with the CareView 1500Cw is shown
in figure 13.
X-ray Tube
Sync Box
X-ray Generator
USB/RS232 Cable
IEEE802.11n
Network Cable
CareView 1500Cw
Wireless AP
DROC Workstation Shielded X-ray Room
Figure 13 Soft sync mode of DR system
6.3.2 Manual Sync Mode

There is no interaction of sync exposure signal between the detector and X-ray generator.
Users should control the exposure time manually according to exposure

recommendations provided by acquisition software.
Note:
1) In manual sync mode, the image will be light and shade no-uniform acquired in the
forbidding exposure time window.
2) If there is no goal image, first check the exposure dose to see whether it is too low,
then check the field view of tube to see whether it covers the plate.
The typical manual sync mode of DR system integrated with the CareView 1500Cw is
shown in figure 14.
C
X-ray Tube
Control Panel
X-ray Generator
Network Cable IEEE 802.11n
DROC Workstation
CareView 1500Cw
Wireless AP
Shielded X-ray Room
Figure 14 Manual sync mode of DR system
6.3.3 Auto Sync Mode

There is no interaction of sync exposure signal between the detector and X-ray generator.
Users can take to exposure at any time after the hints of permitting to exposure.
The DR system in auto sync mode is the same as the connection of manual sync mode.
Note: If there is no goal image, first check the exposure dose to see whether it is too low,

then check the field view of tube to see whether it covers the plate.
7 Packing and Contents
Table 18 Packing and contents

CareView 1500Cw detector Li-Polymer battery
Charging dock Switching power supply
AC Power cable (not included) Power box
Interface cable Others

CD(API, Operation Manual)
Warranty Card
Certification
Packing List
8 Installation
8.1 Hardware Installation
This section describes how to connect the CareView 1500Cw flat panel detector.
Installation of this device should be made by licensed and authorized personnel.
Note: Do not cover or block the wireless module of the detector. Otherwise, the
transmission speed or operable distance may be reduced.
1 Place a fully charged battery pack to the detector
To place the battery pack, first slide the lock lever to open the rear cover of battery
compartment. Then slide the battery pack into the battery compartment. Make sure
that the claws on the battery pack are aligned with the groove on the battery
compartment. Slide the lock lever until it clicks into place.

Figure 15 Place the battery
2 Press the power button of the detector for approximate 3 seconds to turn on the
detector. Make sure the ‘Power LED’ to turn green.
Power LED
Figure 16 Turn on the detector
3 Connect one end of the LAN cable to wireless AP and power it on. Connect the other
end to the LAN Card Connector of workstation assigned for the data transfer.
Note: The wireless AP selection and configuration refer to “Wireless Configuration and
AP selection user guide”.
Figure 17 Connection wireless AP and workstation

8.2 Network Configuration
The default IP address of CareView 1500Cw is 192.168.68.1. Set up the IP address
(192.168.68.100) of image workstation properly prior to the use. The network setup
process is shown below.
Note: The default operation system of the image workstation is windows7. Any other
systems such as windows XP / vista shall be followed the same instruction. Don’t
elaborate the particulars here.
1 Open the “Network and Sharing Center”
Figure 18
2 Open the “Local Area Connection”

Figure 19
3 Check the “properties” of the Local Area Connection Status
Figure 20

4 Choose “Internet Protocol Version 4 (TCP/IPv4) and click OK button. Setup the IP
address as shown below and click the “OK” button to close the dialog box.
Figure 21
5 Affirm the network connection of workstation is 1.0Gbps.
Figure 22 Affirm network speed

6 Network testing
 Launch the commend window and execute “ping 192.168.68.10” to check the
network connection with wireless AP;
 Launch the commend window and execute “ping 192.168.68.1” to check the
network connection with detector.
Figure 23 Network testing
8.3 Turn off the device
1 When you have finished using the detector, Press and hold the power button of the
detector for 3 seconds to turn off the detector.
2 Remove the battery pack if the detector will not be used for some time. Otherwise,
over discharge may occur, resulting in shortened battery life. To remove the battery

pack, slide the battery lock lever to release it, put your fingers on the battery
compartment groove that lifts up the battery and pull it out. Then place the rear cover
of battery compartment well.
9 Announcement
9.1 Basic Notices
Please read this operation manual carefully before using the product in order to ensure
safety and correct usage. Keep it available for reference.
9.1.1 Operation Conditions

 Temperature range: 5℃ ~ 35℃
 Relative humidity: 30% RH ~ 75% RH
 Atmospheric pressure: 700hPa ~ 1060hPa
 Keep away from inflammable gas, corrosive gas, floating dust, and electro-magnetic
waves
9.1.2 Use-method of Power Supply

First connect the power box with detector, and then connect AC power box when power
on. Do not plug forcedly when not well connected as it may result in damage to the power
interface port.
First shut off the power switch, then pull off the connector of AC power box when power
off.
Do not use force when unplugging the power cable between the power box and detector
as it may result in a short circuit, device damage or fire.
9.1.3 Network
The network used between the DROC station and detector should not be connected to
public Ethernet, otherwise will reduces the data transmission speed and brings network
connection invalid or safety problems.
Note: In case the network link is extended, the LAN cable must be FTP or STP type,

category 5 or above (5E or 6).
9.1.4 Electromagnetic Radiation

This product may malfunction due to electromagnetic waves caused by portable personal
telephones, transceivers, radio-controlled toys, etc. Be sure to keep away from the
electro-magnetic objects or fields which affect the detector operation.
To reduce the electric shock hazard, the system must be connected to an electrical
ground. A three conductor AC power cable is supplied with this system to provide the
proper electrical grounding.
9.1.5 Contraindication
Pregnant or lactating women should exercise causation when operating this equipment.
9.2 Particular Notices
9.2.1 Personnel
The instrument must be operated by a qualified engineer. Besides assembling,
adjustment, examination and maintenance must be conducted by trained staff.
9.2.2 X-ray Scope

The active matrix geometry of CareView 1500Cw is 433.7mm*354.8mm as shown in
below figure. Make sure the X-ray exposure area is within the scope.
Figure 24 Active matrix geometry

9.2.3 Operation Conditions
Please use the product in the required operating conditions. Any errors in storage,
transportation and operation may reduce the product performance, shorten the product
usage time, or result in irreparable damage.
Sudden temperature change may cause condensation, leading to poor image quality or
short circuit. Please refrain from use until operating temperature becomes mild and
stable.
Product should not be used in the vicinity of water and dust, which may cause short circuit
or fire.
10 Maintenance
The product must be maintenance by a qualified engineer only. For safety reasons, be
sure to turn OFF the power and unplug the power cables of each device during
maintenance procedures. Failure to do so may result in electric shock.
It is recommended that a record of the inspection be kept by making copies of the check
lists in this section, or making a separate check list.
10.1 Inspections
For safety reasons, please inspect the product before use. If any problem is found during
the inspection, corresponding measures should be taken. If problem still can’t be resolved,
contact the distributor. In addition, regular inspection should be done at least once a year.
Table 19 Inspection item
Item Period Method Description Remedy
Daily or Check that cables are not Contact distributor or

Visual
Cables damaged or cover of cables CareRay if there is any
Weekly inspection
is not torn. problem.
Check that the plugs and
Daily or Visual Fully insert the cables
Connectors locks of connectors are not
Weekly inspection and lock them.
loose.

Check that the cover or Contact distributor or
Daily or Visual
Detector parts are not damaged and CareRay if there is any
Weekly inspection
not loose. problem.
Contact distributor or
Daily or Test Check the exposure
Test exposure CareRay if there is any
Weekly exposure condition of the product
problem.
Exposure a
Monthly phantom Contact distributor or
Check the general
performance or object or a CareRay if there is any
performance of the product
Yearly resolution problem.
chart
We recommend the user to use the phantom or equivalent phantom as following
information:
Manufacturer: Supertech. Inc.
Item Number: 07-646
Dimensions: 17" L X 14" W X 2.5" Thick (43cm X 36cm X 6 cm)
10.2 Maintenance
The instrument must be repaired by a qualified engineer only. If it is not repaired properly,
it may cause fire, electric shock or accident.
If any parts need to be replaced, check the product specification to make sure it is
consistent with the specifications stated in the operation manual. For system performance
and safety purpose, choose the OEM accessories.
 Calibration
Detector is required for calibration for the initial use or three months interval for better
image quality due to X-ray exposure and components degradation to guarantee image
quality. Please check the related manual provided by the DR system manufacturer to get
the information of the calibration process and methods.
10.3 Cleaning
 External cleaning

Use a dry cloth to clean the surface of the product. Don’t use the strong detergent or
organic solvents to clean the product, which may damage the product and cause
structural weakening. The product must be turned off during cleaning.
 Internal Cleaning
CareView 1500Cw has a completely enclosed design which eliminates the need for
internal cleaning.
Note: Don’t use the abrasive brush, scraper, or acid/alkaline cleaner when cleaning the
product.
10.4 Maintenance Note
Do not open and retrofit the detector as this will invalidate the guarantee of product quality
and service. After-sales service for our product will be provided within maintenance time.
We will not be responsible for product damage or accident in the case of incorrect or
unsafe operation of the product.
Note: The shock sensor is incorporated under the rear cover of detector located near the
handle. The shock sensor is calibrated in such a way that a red color appears if the
detector is submitted to a shock corresponding to a drop of 20cm+ in height. CareRay
doesn’t guarantee the performance of the detector in any case if it is red and free
maintenance will not be provided.
11 Storage and Transportation
11.1 Storage
Keep dry ( ) and well ventilation, keep away from the strong sunlight ( ) and
corrosive gas. No inversion ( ), no heap up more than three floors ( ), the
maximum weight is 100kg. Unpack and check every two months. Turn on the power 2

hours in the normal operation environment to ensure the detector works normally. Then
pack it again and store in the required environment.
11.2 Transportation
The packing instructions for the detector are as follows.
 Pack the detector with a special antistatic bag and seal.
 Place the EPE damping foam on the two ends of the detector.
 Put the detector into the packing box and make sure the X-ray incidence surface is
placed in an upward position ( ).

The transportation modes and conditions should be established in the purchases and
sales contract. Avoid inversion, mechanical collision and keep dry during transportation.
12 Emergency
In the occurrence of any of the situations below, immediately turn OFF the power of each
instrument and unplug the power cable from the AC outlet. In case of an accident, guide
the patient far away from the X-ray exposure area.
 Smoke, odd smell or abnormal sound.
 The X-ray continues to expose or not expose at all during the diagnostic process.
 Excessively high temperature of the detector.
 When the instrument has been dropped and it is damaged.
13 Disposal
This equipment has required the extraction and use of natural resources for its production.
It may contain hazardous substances for health and environment. In order to avoid the
dissemination of those substances into the environment and to diminish the pressure on
natural resources, a take-back system should be used. Such systems will reuse or recycle
most of the materials of your end-lift equipment in a sound way.

The crossed-out wheeled bin symbol invites you to use those systems. If you need
more information on the collection, reuse and recycling systems, please contact your local
or regional waste administrator. You can also contact us for more information on the
environment performance of our products.
14 Appendix A
EMC Guidance and Manufacturer’s Declaration
This product complies with the EMC standard IEC 60601-1-2:2007.
Note:
1. The system should not be used adjacent to or stacked with other equipment. If the
adjacent or tacked use is necessary, the system should be observed to verify normal
operation in the configuration in which it will be used.
2. The system needs special precautions regarding EMC and needs to be installed and
put into service according to the EMC information provided below.
3. Preventing conducted RF immunity. Due to technological limitations, the conducted RF
immunity level are limited to 1Vrms level, conducted RF interference above 1Vrms may
cause wrong diagnosis and measurements. We suggested that you position the system
further from sources of conducted RF noise.
4. Portable and mobile RF communications equipment can affects this system.

Lotus Global Co., Ltd.
1 Four Seasons Terrace West Drayton,
Middlesex London, UB7 9GG United Kingdom
Tel: 0044-20-75868010 , 0044-20-70961611
Fax: 0044-20-79006187
CareRay Digital Medical System Co., Ltd.
Address: A2-201/B3-501, Biobay, 218 Xinghu Street, SuZhou Industrial
Park, SuZhou 215123, P. R. China
Tel: (86) 512-86860288 400 635 4696
Fax: (86) 512-86860388
E-mail: info@careray.com

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Technical Files RD-OI-16

Title: CareView 1500Cw Operation Manual Total: 55 pages

Editor Auditor Approval

2015.01.19 Initial Release Leilei. Li

2015.03.02 Updated Leilei. Li

2015.03.10 Delete wireless AP and software information Leilei. Li

Before using the instrument, be sure to read this manual thoroughly.

Page 1 of 55 RD-OI-16 A/0

No part of this document may be reproduced, translated, or transmitted without the

express written permission of CareRay Digital Medical System Co., Ltd.

the product without prior notice.

incurred in connection with furnishing or use of this manual.

This manual is intended to help Original Equipment Manufacturers in the installation of

radiography system. The equipment manufacturer or retrofitter is also responsible of the

validation of the CareView 1500Cw performance for the foreseen application.

CareView 1500Cw. Consult CareRay for additional information.

Page 2 of 55 RD-OI-16 A/0

the environment with strong electromagnetic field.

supply mains with protective earth.

recommended by CareRay to avoid unnecessary risks.

Page 3 of 55 RD-OI-16 A/0

Warning: Do not modify this equipment without authorization of the MANUFATURER.

Warning: If this equipment is modified, appropriate inspection and testing must be

conducted to ensure continued safe use of the equipment.

applicable in your area.

Battery Pack and Battery Charger Safety Information

Warning: The change of Li-polymer battery must be operated by a qualified engineer.

leak may occur, resulting in fire or electrical shock.

other liquids and do not allow them to get wet.

Page 4 of 55 RD-OI-16 A/0

dose of ionizing radiation is higher), and so unnecessary radiation exposure is of

particular concern for pediatric patients.

the examination to insure correct study is being performed.

Page 5 of 55 RD-OI-16 A/0

CAN/CSA-C22.2 No. General Requirements for Basic Safety and Essential

IEC/EN 60601-1-2 Medical electrical equipment

IEEE 802.11a/b/g/n Wireless Communications

Radio Frequency (RF) compliance information

European Union EN 300328 V1.8.1

Page 6 of 55 RD-OI-16 A/0

(1) This device may not cause harmful interference.

cause undesired operation.

reasonable protection against harmful interference when the equipment is operated in a

may cause harmful interference to radio communications. Operation of this equipment in

required to correct the interference at his own expense.

(1) For operation within 5.15~5.25GHz frequency range, it is restricted to indoor

Page 7 of 55 RD-OI-16 A/0

an electromagnetically noisy location. Attempt to maintain a suitable distance between

electrical devices to prevent malfunction.

Harmonic emissions and those directly connected to the public

Voltage fluctuations/ buildings used for domestic purposes.

flicker emissions Complies

Page 8 of 55 RD-OI-16 A/0

±2㎸ for ±2㎸ for

IEC 61000-4-4 ± 1 ㎸ for ± 1 ㎸ for environment.

differential differential Mains power quality should be that

Page 9 of 55 RD-OI-16 A/0

Power frequency Power frequency magnetic fields

(50/60 ㎐) should be at levels characteristic of

IEC 61000-4-8 commercial or hospital environment.

IEC 60601 Compliance Electromagnetic Environment –

Recommended separations distance

where P is the maximum output power