Compal Electronics SHC100 Single Stream 802.11a/b/g/n/ac + BT 4.1 M.2 Type Card User Manual

Compal Electronics Inc Single Stream 802.11a/b/g/n/ac + BT 4.1 M.2 Type Card Users Manual

Contents

User Manual-1

User Manual
Healthcare Information Terminal
SHC-100
版次：
0.7
文件日期： 2018/07/16
仁寶電腦工業股份有限公司
Compal Electronics, Inc.
SHC-100
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Instructions for the User
The document combines text and illustrations, providing a comprehensive overview of the system.
The information is presented as sequential steps of actions, allowing the users to learn directly how to use
the device.
The text provides explanations and instructs the user step-by-step in the practical use of the product,
with short, clear instructions in an easy-to-follow sequence.
Definitions
Avertissement!
A WARNING statement provides important information about a potentially hazardous
situation which, if not avoided, could result in death or serious injury
.
Une déclaration d'AVERTISSEMENT fournit des informations importantes sur une
situation potentiellement dangereuse qui, si elle n'est pas évitée, pourrait
entraîner la
mort ou des blessures graves.
Attemtion!
A CAUTION statement provides important information about a potentially hazardous
situation which, if not avoided, may result in minor or
moderate injury to the user or
patient or in damage
to the equipment or other property.
Une déclaration de
ATTENTION fournit des informations importantes sur une situation
potentiellement dangereuse qui, si elle n'est pas évitée, peut entraîner des blessures
mineures ou modérées pour l'utilisateur ou
le patient ou endommager l'équipement ou
d'autres biens.
Remarque!
A NOTE provides additional information intended to avoid inconveniences during
operation.
Une REMARQUE fournit des informations supplémentaires destinées à éviter les
désagréments pendant le fonctionnement.
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Safety Instructions
Strictly follow these instructions for use, please read these safety instructions carefully. Remember
to keep this user manual for later reference, and that any use of the product requires the full understanding
and strict observation of all portions of these instructions. Observe all WARNINGS and CAUTIONS as
rendered throughout this manual and on labels on the equipment.
Installation and repair of the device shall only be carried out by manufacturer authorized and trained
service personnel. Otherwise, the correct functioning of the device may be compromised.
Avertissement!
Installation is only to be carried out by manufacturer authorized and trained personnel.
Because of the
danger of electric shock, never remove the cover of a
device while it is in
operation or connected to a power outlet.
L'installation doit uniquement être effectuée par un fabricant autorisé et formé
.
En raison du risque d'électrocution, ne retirez jamais
le couvercle d'un appareil
lorsqu'il est en fonctionnement ou connecté à une prise de courant.
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If one of the following situations arises, get the equipment checked by service personnel:
The power cord or plug is damaged.
Liquid has penetrated into the equipment.
The equipment has been exposed to moisture.
The equipment does not work well, or you cannot get it to work according to the user manual.
The equipment has been dropped and damaged.
The equipment has obvious signs of breakage.
Disconnect this equipment from any AC outlet before cleaning. Use a damp cloth. Do not use liquid or
spray detergents for cleaning and keep this equipment away from humidity.
Attemtion!
To avoid short-circuiting and otherwise damaging the device, do not allow fluids to
come in contact with the device. If fluids are accidentally
spilled on the equipment,
remove the affected unit from service as soon
as possible and contact the service
personnel to verify that patient
safety is not compromised.
Pour éviter les courts
-circuits et l'endommagement de l'appareil, ne laissez pas les
liquides entrer en contact avec l'appareil. Si des liquides sont renversés
accidentellement sur l'équipement, retirez l'unité touchée du service dès que possible
et
contactez le personnel de service pour vérifier que la sécurité du patient n'est pas
compromise.
Put this equipment on a stable surface during installation. Dropping it or letting it fall may cause damage.
For plug-in equipment, the power outlet socket must be located near the equipment and must be easily
accessible.
Attemtion!
To prevent overheating, do not cover the openings or place the device in direct sunlight
or near radiant heaters.
Pour éviter toute surchauffe, ne couvrez pas les
ouvertures et placez l'appareil à la
lumière directe du soleil ou à proximité de radiateurs radiants.
Make sure the voltage of the power source is correct before connecting the equipment to the power outlet.
Position the power cord so that people cannot step on it. Do not place anything over the power cord. If the
equipment is not used for a long time, disconnect it from the power source to avoid damage by transient
overvoltage.
Attemtion!
Do not leave this equipment in an uncontrolled environment where the storage
temperature is below
-20° C (-4° F) or above 60° C (140° F). This may damage the
equipment.
Ne laissez pas cet équipement dans un environnement non contrôlé où la température de
stockage est inférieure à
-20 ° C (-4 ° F) ou supérieure à 60 ° C (140 ° F). Cela peut
endommager l'équipement.
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If your computer has lost its date and time settings or the BIOS configuration has been reset to its default
settings, the battery has no power.
Attemtion!
Do not replace the battery yourself. Please contact a qualified technician or your
retailer.
The computer is supplied with a battery
-powered real-time clock circuit.
There is a danger of explosion if the battery is incorrectly replaced. Replace
only with
the same or equivalent type
recommended by the manufacturer.
Discard used batteries according to the manufacturer’s instructions
.
A battery charge indicator is not included with this device. It will be
added to the
finished system assembly and be shown with the completed
system.
Ne
remplacez pas la batterie vous-même. Veuillez contacter un technicien qualifié ou
votre revendeur.
L'ordinateur est équipé d'un circuit d'horloge en temps réel alimenté par batterie.
Il existe un risque d'explosion si la batterie est incorrectement rempla
cée. Remplacez
uniquement par le même type ou un type équivalent recommandé par le fabricant.
Jetez les piles usagées conformément aux instructions du fabricant.
L'indicateur de charge de la batterie n'est pas inclus avec cet appareil. Il sera ajouté à
l'assemblage du système fini et montré avec le système terminé.
Improper installation of VESA mounting can result in serious personal injury! VESA mount installation
should be operated by a professional technician, please contact the service technician or your retailer if
you need this service. The detailed operating procedure is specified in chapter 3.4.
Classification:
I. Supply Class I adapter
II. No applied part
III. IPX1 compliant
IV. Continuous Operation
V. Not AP or APG category
Avertissement!
This device is not suitable for use in the presence of flammable anesthetic mixture with
air, oxygen, nitrous oxide, or for life support system.
Ce dispositif ne convient pas à une utilisation en présence d'un mélange anesthésique
inflammable avec de l'air, de
l'oxygène, de l'oxyde nitreux ou pour un système de
support de vie.
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Environmental protection: follow national requirements to dispose of the unit.
Maintenance: to properly maintain and clean the surfaces, use only the approved products or clean with a
dry applicator.
Attemtion!
When servicing the device, always use replacement parts that meet Compal standards.
Compal
products cannot warrant or endorse the safe performance of third-party
replacement parts for use
with our device.
Lors de l'entretien de l'appareil, utilisez toujours des pièces de rechange conformes aux
normes Compal. Le produit Compal ne peut pas garantir ou endosser les performances
sécuritaires des pièces de rechange tierces à utiliser avec notre appareil.
Make sure the user does not contact SIP/SOPs and the patient at the same time.
When networking with electrical devices, the operator is responsible for ensuring that the resulting system
meets the requirements set forth by the following standards:
IEC 60601-1
Medical electrical equipment
Part 1: General requirements for safety
IEC 60601-1-2
Medical electrical equipment
Part 1-2: General requirements for safety
Collateral standard: Electromagnetic compatibility; Requirements and tests
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Accessory equipment connected to the analog and digital interfaces must be in compliance with the
respective nationally harmonized IEC standards (i.e. IEC 60950 for data processing equipment, IEC
60065 for video equipment, IEC 61010-1 for laboratory equipment, and IEC 60601-1 for medical
equipment.) Furthermore, all configurations shall comply with the system standard IEC 60601-1-1.
Everybody who connects additional equipment to the signals input part or signals output part configures a
medical system and is therefore responsible that the system complies with the requirements of the system
standard IEC 60601-1-1. The unit is for exclusive interconnection with IEC 60601-1 certified equipment
in the patient environment and IEC 60XXX certified equipment outside of the patient environment. If in
doubt, consult the technical services department or your local representative.
Attemtion!
Use suitable mounting apparatus to avoid the risk of injury.
Utiliser un appareil de montage approprié pour éviter le risque de ble
ssure.
Grounding reliability can only be achieved when the equipment is connected to an equivalent receptacle
marked "Hospital Only" or "Hospital Grade".
Use a power cord that matches the voltage of the power outlet, which has been approved and complies
with the safety standard of your particular country.
Remarque!
Environmental protection
Follow national requirements to dispose of the unit.
Protection environnementale
Suivez les exigences nationales pour disposer de l'unité.
Avertissement!
Do not modify this equipment without the authorization of the manufacturer.
Ne modifiez pas cet équipement sans l'autorisation du fabricant.
Avertissement!
To avoid the risk of electric shock, this equipment must only be connected to supply
mains
with protective earth.
Pour éviter tout risque d'électrocution, cet équipement doit uniquement être raccordé au
réseau d'alimentation avec une terre de protection.
Attemtion!
This adapter DELTA MDS-060AAS19 B is a forming part of the medical device.
Cet adaptateur DELTA MDS
-060AAS19 B fait partie du dispositif médical.
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Avertissement!
To turn off the power, please disconnect the power cord.
Pour éteindre l'appareil, débranchez le cordon
d'alimentation.
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Explanation of Graphical Symbols
IEC 60878 and ISO 3864
-B.3.6 : Warning: dangerous voltage.
CEI 60878 et ISO 3864
-B.3.6: Avertissement: tension dangereuse.
ISO 7000-0434: Caution, consult ACCOMPANYING DOCUMENTS.
ISO 7000-0434: Attention, consulter les DOCUMENTS D'ACCOMPAGNEMENT.
ISO 7000-1641: Follow operating instructions or Consult instructions for use.
ISO 7000-1641: Suivre les instructions d'utilisation ou Consulter les instructions d'utilisation.
IEC 60417
- 5009: STAND-BY.
CEI 60417
- 5009: STAND-BY.
IEC 60417-5031: Direct current.
CEI 60417-5031: Courant continu.
ISO 7010
-M002: Refer to instruction manual/booklet
ISO 7010
-M002: Se reporter au manuel d'instructions / livret
IEC 60417-5032: Alternating Current
CEI 60417-5032: Courant Alternative
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Federal Communication Commission (FCC) Interference
Statement - Clase B
This device complies with Part 15 of the FCC Rules. The operation is subject to the following two
conditions: (1) This device may not cause harmful interference, and (2) this device must accept any
interference received, including interference that may cause undesired operation.
This equipment has been tested and found to comply with the limits for a Class B 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 residential environment. This
equipment generates uses and can radiate radio frequency energy. If not installed and used in
accordance with this user's manual, it may cause harmful interference to radio communications. Note
that even when this equipment is installed and used in accordance with this user's manual, there is still
no guarantee that interference will not occur. If this equipment is believed to be causing harmful
interference to radio or television reception, this can be determined by turning the equipment on and off.
If interference is occurring, the user is encouraged to try to correct the interference by one or more of
the following measures:
Reorient or relocate the receiving antenna
Increase the separation between the equipment and the receiver
Connect the equipment to a power outlet on a circuit different from that to which the receiver is
connected
Consult the dealer or an experienced radio/TV technician for help
Avertissement!
Any changes or modifications made to the equipment which are not expressly approved
by the relevant standards authority could void your
authority to operate the equipment.
Tout changement ou modification apporté à l'équipement qui n'est pas expressément
approuvé par l'autorité de normalisation concernée peut annuler votre droit
d'utiliser
l'équipement.
FOR MOBILE DEVICE USAGE (>20cm)
Radiation Exposure Statement:
This equipment complies with FCC radiation exposure limits set forth for an uncontrolled environment.
This equipment should be installed and operated with minimum distance 20cm between the radiator &
your body.
FOR COUNTRY CODE SELECTION USAGE (WLAN DEVICES)
Note: The country code selection is for the non-US model only and is not available to all US model. Per
FCC regulation, all WiFi product marketed in the US must fix to US operation channels only.
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Additional Information and Assistance
Contact your distributor, sales representative, or Compal's customer service center for technical support if
you need additional assistance. Please have the following information ready before you call:
Product name and serial number
Description of your peripheral attachments
Description of your software (operating system, version, application software, etc.)
A complete description of the problem
The exact wording of any error messages
This equipment is a source of electromagnetic waves. Before use please, make sure that there are not
EMI sensitive devices in its surrounding which may malfunction, therefore.
Manufacturer
COMPAL ELECTRONICS, INC.
NO.581, Ruiguang Rd., Taipei City 11492,
Taiwan, R.O.C.
TEL: 886-2-87978599
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Revision History
Version Date Description Author Reviewed by Approved by
V0.1
2018.05.10
Init Version
Bo
V0.2
2018.05.29
Add RoHS, remove EU
Bo
V0.22
2018.06.08
modify
Bo
V0.3
2018.06.11
Add lab suggestion
Bo
V0.31
2018.06.12
Add lab suggestion
Bo
V0.4
2018.06.14
Add TS and modify the spec
Bo
V0.41 2018.06.26
ISO 7000-1641 &
ISO 7010-M002
Bo
V0.5
2018.06.27
Installation warning
Bo
V0.6
2018.07.06
Add French Warning
Bo
V0.7 2018.07.16
Add control setting and
modify certification level
Bo
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Contents
CONTENTS ............................................................................................................................................. XII
CHAPTER 1 GENERAL INFORMATION ............................................................................................. 1
1.1 INTRODUCTION ................................................................................................................................. 1
1.1.1 Intended Use ...................................................................................................................... 1
1.2 DIMENSIONS ..................................................................................................................................... 2
1.3 BUTTONS AND REAR I/O .................................................................................................................. 3
1.4 OPTIONAL MODULES ........................................................................................................................ 6
1.5 CLEANING AND DISINFECTING .......................................................................................................... 7
1.6 INTENDED USER PROFILE .................................................................................................................. 9
CHAPTER 2 HARDWARE DESCRIPTION ......................................................................................... 11
2.1 SPECIFICATIONS .............................................................................................................................. 11
2.2 EXTERNAL VIEW ............................................................................................................................ 13
2.2.1 Front View ........................................................................................................................... 13
2.2.2 Side View ............................................................................................................................. 13
2.2.3 Rear View ............................................................................................................................ 14
CHAPTER 3 INSTALLATION ............................................................................................................... 15
3.1 INSTALLATION PROCEDURES .......................................................................................................... 15
3.1.1 Connecting the Power Cord ................................................................................................. 15
3.1.2 Switching on the power ....................................................................................................... 16
3.2 RUNNING THE BIOS SETUP PROGRAM ........................................................................................... 17
3.3 INSTALLING SYSTEM SOFTWARE .................................................................................................... 17
3.4 INSTALL VESA MOUNTING ............................................................................................................ 18
3.5 TROUBLESHOOTING ........................................................................................................................ 19
CHAPTER 4 SOFTWARE ....................................................................................................................... 20
4.1 DISPLAY CONTROL SETTINGS ......................................................................................................... 20
4.2 WINDOWS DRIVERS LIST ................................................................................................................ 22
CHAPTER 5 APPENDIX ......................................................................................................................... 23
5.1 ANNEX ........................................................................................................................................... 23
5.1.1 Guidance and manufacturer’s declaration – electromagnetic emissions ......................... 23
5.1.2 Recommended separation distances between portable and mobile RF communications
equipment and the model SHC-100 ................................................................................ 23
5.1.3 Guidance and manufacturer’s declaration – electromagnetic immunity ......................... 24
5.1.4 Guidance and manufacturer’s declaration – electromagnetic immunity ......................... 25
5.1.5 Names and contents of harmful substances in products (TW) ........................................ 26
5.1.6 产品中有害物质的名称及含量 (China) ........................................................................ 27
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Chapter 1 General Information
1.1 INTRODUCTION
The SHC-100 is a high-quality medical grade AIO (All-in-One) computer. It is a PC-based
system with an Intel® Core™ i5 processor, 21.5” widescreen TFT LCD display, 2.5” SATA and M.2
PCI-E hard drive, up to 32 GB DDR4 RAM and a capacitive multi-touch screen that enhances the
efficiency of hospital applications with glove-tolerant capabilities. It also features a dual-band
802.11 a/b/g/n/ac, Bluetooth 4.1 and NFC module. The fan-less design keeps its surrounding
environment quiet while enhancing infection control. IPS technology provides the SHC-100 with the
best image solution. With standard VESA mounting holes on the rear of the system, any standard
mount or stand can be installed to enhance the application experience.
1.1.1 Intended Use
The SHC-100 is intended to serve as a multimedia system that integrates with hospital systems.
Furthermore, the SHC-100 is designed for general purpose medical computing in the hospital
environment, data collection, and displaying information. It should not be used as a life-support
system nor for diagnostic purposes.
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1.2 DIMENSIONS
Dimensions: 535.2(W) x 375.7(H) x 50.4(D) mm
Figure 1.2-1 Dimensions
VESA Mounting Dimensions: 75 x 75 mm; 100 x 100 mm
Figure 1.2-2 VESA Mounting Dimensions
Avertissement!
Use suitable mounting apparatus to avoid the risk of injury.
Utiliser un
appareil de montage approprié pour éviter le risque de blessure.
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1.3 BUTTONS AND REAR I/O
Figure 1.3-1 SHC-100 Front View
○
1 Power Button
○
2 NFC Reader
○
3 Camera
Fig 1.3-2 SHC-100 Top View
○
1 Lens Cover Switch (for Camera)
○
2
○
1
○
3
○
1
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Figure 1.3-3 SHC-100 Rear View
○
1 VESA Mount
○
2 DC-In Power Port
○
3 Gigabit Ethernet Port (RJ-45)
○
4 HDMI Out Port
○
5 USB 2.0 Port x 3
○
6 USB 3.0 Port x 1
○
7 RS-232 Port
○
8 Kensington Lock Slot
○
9 External Antennas
○
1
○
2
○
3
○
4
○
5
○
6
○
7
○
8
○
9
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Figure 1.3-4 SHC-100 Side Views (Left and Right)
○
1 Smart Card Reader
○
2 USB 2.0 Port
○
3 SD Card Reader
○
4 Combo Audio Jack
○
5 Power Button
○
6 [Optional] RS-232 Port*
○
7 [Optional] USB 2.0Port x 3*
○
8 [Optional] Optical Disc Drive (ODD)*
*Items 6 and 7 are components featured on the optional accessory board which can be switched to
item 8.
Figure 1.3-5 SHC-100 Bottom View
○
1 Rear Cover Locks (Open: Turn Counterclockwise, Close: Turn Clockwise)
○
1
○
1
○
2
○
3
○
4
○
6
○
7
○
8
○
5
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1.4 OPTIONAL MODULES
Memory: 4GB or 8GB DDR4 2400/2666 SDRAM
SSD: M.2 PCIe 256GB SSD
Hand Set: USB Phone holder
Accessory Board: (1) RS-232 and USB 2.0 x 3
(2) ODD
Antenna: 3 dB External Antenna x 2
Stand: Standard VESA 100 x 100 mm table stand
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1.5 CLEANING AND DISINFECTING
During normal use of the SHC-100, the device may become dirty and as a result should be
regularly cleaned.
Steps:
1. Prepare a cleaning agent per manufacturer's instructions or hospital protocol.
2. Wipe the SHC-100 with a clean cloth that has been moistened by the cleaning agent.
3. Wipe thoroughly with the clean cloth.
Cleaning agent list: chemical disinfectants which have been tested on the SHC
No.
Cleaning Agents
1 Ethyl alcohol 70%
2 Isopropyl alcohol 70%
Attemtion!
Do not immerse or rinse the SHC or its peripherals. If you accidentally spill liquid
on the device, disconnect the unit from the power source. Contact your Biomed
Department regarding the continued safety of the unit before placing it back in
operation.
Do not spray cleaning agent on the chassis.
Do not use disinfectants that contain phenol. Do not autoclave or clean the SHC
or
its peripherals with strong aromatic, chlorinated,
ketone, ether, or Esther solvents,
sharp tools or abrasives. Never immerse electrical connectors in water or other
liquids.
Do not scratch the surface of the screen with any hard objects.
Do not spray liquid directly on the screen or allow excess liquid to drip down
inside the device.
Do not place anything, such as food and drink, on the screen at any time to preve
nt
damage to the screen.
Clean the LCD display only with a soft cloth dampened with 70% above isopropyl
alcohol or 70% ethyl alcohol.

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