IEI Technology HTB-100-HM170 User manual

Fanless Medical Embedded System with
Intel® Core™ i7-6822EQ/i5-6442EQ Processor, Isolated COM Ports,
GbE LAN, HDMI, VGA, USB 3.0, Audio and RoHS Compliant
HTB-100-HM170
Quick Installation Guide
Version 1.00
©2018 Copyright by IEI Integration Corp.
All rights reserved.

1
Revision
Date
Version
Changes
July 2, 2018
1.00
Initial release
Intended Use
The HTB-100-HM170 medical embedded system is intended to serve as a Medical
Embedded System for integration with the hospital system. The Medical Embedded
System is designed for general purpose for hospital environment. For data
collection and process for reference, include Surgical, Radiology, LIS (Lab
Information Systems) and Electronic Medical Record. It shall not be used for
life-supporting system.
Manual Conventions
WARNING
Warnings appear where overlooked details may cause damage to the
equipment or result in personal injury. Warnings should be taken
seriously.
CAUTION
Cautionary messages should be heeded to help reduce the chance of
losing data or damaging the product.
NOTE
These messages inform the reader of essential but non-critical
information. These messages should be read carefully as any
directions or instructions contained therein can help avoid making
mistakes.
Hot surface
This symbol indicates a hot surface that should not be touched without
taking care.
OPERATING INSTRUCTION
Follow operating instructions or consult instructions for use.
IEC 60417-5009: Stand-by
IEC 60417-5021: Equipotentiality
IEC 60417-5032: Alternating Current
Direct current

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Overview
The HTB-100-HM170 fanless medical embedded system is powered by
Intel® Core™ i7-6822EQ or Intel® Core™ i5-6442EQ processor. It is
designed for medical applications that require reliable operating and easy
maintenance features.
The HTB-100 is compliant with medical standards, including IEC 60601-1
V3.1, IEC 60601-1-2 V4.0, ISO 14971 and FCC part 18 Class B, making
the medical environment more reliable.
All of the COM ports support 2.5 kV isolation that meets medical standard.
The display interface options include VGA and HDMI with three audio jacks.
The HTB-100-HM170 series systems are all capable of supporting one 2.5”
SATA 6Gb/s solid-state drive (SSD) or an mSATA module.
WARNING:
Please do not touch patient and this medical device at the same time.

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Front Panel
Rear Panel

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System Specifications
HTB-100-HM170
CPU Intel® Core™ i7-6822EQ 2.0 GHz
(up to 2.8 GHz, quad-core, 25W TDP)
Intel® Core™ i5-6442EQ 1.9 GHz
(up to 2.7 GHz, quad-core, 25W TDP)
Chipset Intel® HM170
System Memory 2 x 260-pin DDR4 SO-DIMM slot (system max. 32 GB)
Preinstalled one 4.0 GB DDR4 SDRAM SO-DIMM
Thermal Solution Fanless
Ethernet 2 x RJ-45 PCIe GbE by Intel® I211 Ethernet controller
Display 1 x HDMI 2.0 port (up to 4096x2160 @ 60 Hz)
1 x VGA port (up to 1920x1200 @ 60 Hz)
Serial Port 2 x RS-232 (DB-9 with 2.5 kV isolation)
2 x RS-232/422/485 (DB-9 with 2.5 kV isolation)
USB 2 x USB 2.0 ports
4 x USB 3.0 ports
Audio Realtek ALC662 5.1-channel High Definition Audio (HDA)
1 x Audio line-in
1 x Audio line-out
1 x Audio mic-in
Storage 1 x 2.5” SATA 6Gb/s HDD/SSD bay
Expansion 1 x PCIe x16 slot (max. 12 W, 12 V)
1 x Half-size PCIe Mini card slot (max. 7 W, 3.3 V)
1 x Full-size PCIe Mini card slot (max. 7 W, 3.3 V) with mSATA
support (colay with SATA)
1 x M.2 2230 slot (A-key & E-key; USB or PCIe signal; max. 7
W, 3.3 V)
Chassis Construction Extruded aluminum alloy
Power Requirement 12 V–28 V DC

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Power Supply 150 W medical-grade power adapter
Input: 90 V AC ~ 264 V AC, 47 Hz ~ 63 Hz, 2.0 A ~ 0.85 A
Output: 150 W Max., 19 V 7.89 A
Power Consumption 19 V @ 4.4 A (with Intel® Core™ i7-6822EQ processor and 4
GB DDR4 memory)
Operating Shock Half-sine wave shock 5G; 11ms; 100 shocks per axis
Operating Vibration MIL-STD-810G 514.6C-1 (with SSD)
Temperature Operation: 0ºC–40ºC with air flow (SSD)
Storage/Transportation: -40ºC–70ºC with air flow (SSD)
Humidity Operation: 10%–95%, non-condensing
Storage/Transportation: 10%–95%, non-condensing
Pressure Operation: 700 hpa–1060 hpa
Storage/Transportation: 700 hpa–1060 hpa
Color Silver + Grayish blue
Weight (Net/Gross) 2.2 kg / 3.0 kg
Dimensions (W x D x
H)
294 mm x 209 mm x 90.2 mm
Safety/EMC CE, FCC class B part 18, IEC 60601-1 V3.1, IEC 60601-1-2
V4.0,
ISO 14971
IP Rating IP 41 compliant top cover
Supported OS Microsoft Windows 8 or 8.1
Microsoft Windows 10
Microsoft Windows Embedded Standard 7

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Installation Precautions
When installing the medical embedded system, please follow the
precautions listed below:
Manufacturer authorization: Do not modify this equipment
without authorization of manufacturer.
Read the user manual: The user manual provides a complete
description of the medical embedded system, installation
instructions and configuration options.
DANGER! Disconnect Power: Power to the medical embedded
system must be disconnected during the installation process.
Failing to disconnect the power may cause severe injury to the
body and/or damage to the system.
Certified Engineers: Only certified engineers should install and
modify the hardware settings.
Power turned off: When installing the medical embedded system,
make sure the power is off. Failing to turn off the power may cause
severe injury to the body and/or damage to the system.
Anti-static Discharge: If a user open the top cover of the medical
embedded system, to configure the jumpers or plug in added
peripheral devices, ground themselves first and wear an anti-static
wristband.
Grounding Cable Connection
To protect the HTB-100-HM170 from static electricity, the grounding cable
that came with the system has to be connected. To connect the grounding
cable, please follow the steps below.
Step 1: Connect the grounding cable to the equipotentiality terminal on the
rear panel of the HTB-100-HM170 (Figure 3 15).
Step 2: Use the hand clamp on the other end of the grounding cable to clip
on the Earth’s conductive surface.
Mounting the System
WARNING:
The HTB-100-HM170 can only be placed on a desktop or other surface
horizontally. Do not mount the HTB-100-HM170 onto a wall or other
mounting apparatus.

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Powering On the System
WARNING:
To avoid risk of electric shock, this equipment must only be connected to
supply mains with protective earth.
CAUTION:
The power adapter came with the HTB-100-HM170 is a forming part of
the medical device.
CAUTION:
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
over voltage.
Step 1: Connect the power cord to the power adapter. Connect the other
end of the power cord to a power source.
Step 2: Connect the power adapter to the power connector of the
HTB-100-HM170.
Step 3: Short-press the power button on the front panel until the power
LED lights on in blue.
Shutdown Procedure
Turn off the power and disconnect the power cord.
To prevent the risk of electric shock, make sure power cord is
unplugged from wall socket. To fully disengage the power to the unit,
please disconnect the power cord from the AC outlet. Refer servicing to
qualified service personnel. The AC outlet shall be readily available and
accessible.

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Troubleshooting
If the following situations happen, contact your distributor, sales
representatives or IEI customer service center for technical support.
The HDD is installed correctly, but the HTB-100-HM170 is unable to
boot with AC power input after pressing the power button.
Unable to shut down the HTB-100-HM170 normally
Please have the following information prepared prior to reporting the
abnormal situations:
Product name and S/N
OS, BIOS version and applications
A complete description of the abnormal situation (with photos or video
if available)
System Maintenance
If the components of the HTB-100-HM170 fail they must be replaced.
Please contact the system reseller or vendor to purchase the replacement
parts.
Maintenance and Cleaning
WARNING:
1. For safety reasons, turn-off the power and unplug the medical
embedded system before cleaning.
2. If you dropped any material or liquid such as water onto the medical
embedded system when cleaning, unplug the power cable immediately.
Always make sure your hands are dry when unplugging the power cable.
Prior to cleaning any part or component of the HTB-100-HM170, please
read the details below.
To clean the HTB-100-HM170,
oremove dirt with a lightly moistened cloth. Then wipe the external
chassis with a soft dry cloth.
ouse 75% ethanol alcohol to clean the external chassis.
Cleaning frequency: follow the cleaning method guidelines of the
hospital.
Never spray or squirt liquids directly onto any other components.
The interior of the HTB-100-HM170 does not require cleaning. Keep
fluids away from the HTB-100-HM170 interior.
Never drop any objects or liquids through the openings of the
HTB-100-HM170.

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Accessories
The HTB-100-HM170 medical embedded system is shipped with the
following components:
Quantity
Item
Image
1 medical embedded system
1 Power cord
1 Medical-grade power adapter
(150 W, 19 V DC output)
1 Grounding cable
1 HDMI cable holder
5 Screws (M3*4) for HDD installation
1 Spare screw (M2*4) for M.2
installation
2
Spare screws (M2*3) for PCIe Mini
card installation
4 Spare screws (M3*6)
7
Stickers for external chassis screws

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Optional Items
The following are optional components which may be separately
purchased:
Item and Part Number
Image
Cable cover
Wi-Fi kit
(P/N: EMB-WIFI-KIT02E-R10)

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DECLARATION OF CONFORMITY
This equipment is in conformity with the following EU directives:
EMC Directive (2004/108/EC, 2014/30/EU)
Low-Voltage Directive (2006/95/EC, 2014/35/EU)
RoHS II Directive (2011/65/EU, 2015/863/EU)
Medical Device Directive 93/42/EEC: EN 60601-1
If the user modifies and/or install other devices in the equipment, the CE
conformity declaration may no longer apply.
If this equipment has telecommunications functionality, it also complies
with the requirements of the Radio Equipment Directive 2014/53/EU.
IEI Integration Corp declares that this equipment is in compliance with the
essential requirements and other relevant provisions of Directive
2014/53/EU.
FCC WARNING
This equipment complies with part 18 of the FCC Rules.
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 radio communications. However, there is no
guarantee that interference will not occur in a particular installation. If this
equipment does cause harmful interference to radio or television
reception, which can be determined by turning the equipment off and on,
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 receiver.
Connect the equipment into an outlet on a circuit different from that
to which the receiver is connected.
UL CLASSIFIED
Medical general medical equipment with respect to electrical shock, fire
and mechanical hazards only in accordance with ANSI/AAMI ES60601-1
(2005 and Amendment 1), CAN/CSA-C22.2 NO. 60601-1 (2014).
ROHS STATEMENT
The label on the product indicates this product conforms to European
(EU) Restriction of Hazardous Substances (RoHS) that set maximum
concentration limits on hazardous materials used in electrical and
electronic equipment.

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CHINA ROHS
The label on the product indicates the estimated “Environmentally
Friendly Use Period” (EFUP). This is an estimate of the number of years
that these substances would “not leak out or undergo abrupt change.”
This product may contain replaceable sub-assemblies/components which
have a shorter EFUP such as batteries and lamps. These components will
be separately marked.
UL CLASSIFIED
Medical general medical equipment with respect to electrical shock, fire
and mechanical hazards only in accordance with ANSI/AAMI ES 60601-1
(2005) + AMD (2012) and CAN/CSA-C22.2 No. 60601-1: 14.
TÜV SÜD MARK
SAFETY TESTED. PRODUCTION MONITORED
Component carrying this mark was tested and certified by the independent
third-party organization TÜV SÜD Product Service for its conformity with
the safety requirements of EN60601-1.
TÜV RHEINLAND CERTIFIED
Component carrying this mark was tested and certified by the independent
third-party organization TÜV Rheinland Product Service for its conformity
with the safety requirements of EN60601-1 and IEC60601-1.
C-UL-US CERTIFICATE
The UL Recognized Component Mark indicates compliance with UL
requirements, as well as Canadian and U.S. requirements. Components
carrying this mark are covered by UL’s Follow-Up Service program to
determine continued compliance with UL’s requirements.
STANDARD INSPECTION BUREAU FOR CHINA
Authentication sign of the Standard Inspection Bureau for China.

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Safety Precautions
WARNING:
The precautions outlined below should be strictly followed. Failure to
follow these precautions may result in permanent damage to the
HTB-100-HM170.
General Safety Precautions
Please ensure the following safety precautions are adhered to at all times.
To prevent the risk of electric shock, make sure power cord is
unplugged from wall socket. To fully disengage the power to the unit,
please disconnect the power cord from the ac outlet. Refer servicing
to qualified service personnel. The AC outlet shall be readily available
and accessible.
Users must not allow SIP/SOPs and the patient to come into contact
at the same time.
Grounding reliability can only be achieved when the equipment is
connected to an equivalent receptacle marked “Hospital Only” or
“Hospital Grade”.
Make sure the power is turned off and the power cord is disconnected
whenever the HTB-100-HM170 is being installed, moved or modified.
Do not apply voltage levels that exceed the specified voltage range.
Doing so may cause fire and/or an electrical shock. 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.
Accessory equipment connected to the analog and digital interfaces
must be in compliance with the respective nationally harmonized IEC
standards (i.e. IEC 60601-1 for medical equipment.) Furthermore all
configurations shall comply with the system standard in IEC 60601-1.
Anyone who connects additional equipment to the signal input part or
signal output part is configuring a medical system, and is therefore,
responsible that the system complies with the requirements of the
system standard IEC 60601-1. 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.
The equipment should be installed near an easily accessible outlet.
For pluggable equipment, the power outlet must be installed near the
equipment and must be easily accessible.
Electric shocks can occur if the HTB-100-HM170 chassis is opened
when the HTB-100-HM170 is running. To avoid risk of electric shock,

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this equipment must only be connected to a supply mains with
protective earth.
If considerable amounts of dust, water, or fluids enter the
HTB-100-HM170, turn off the power supply immediately, unplug the
power cord, and contact the HTB-100-HM170 vendor.
Product Disposal
CAUTION:
Risk of explosion if battery is replaced by an incorrect type. Only certified
engineers should replace the on-board battery.
Dispose of used batteries according to instructions and local regulations.
Outside the European Union - If you wish to dispose of used electrical
and electronic products outside the European Union, please contact
your local authority so as to comply with the correct disposal method.
Within the European Union–The device that produces less waste
and is easier to recycle is classified as electronic device in terms of
the European Directive 2012/19/EU (WEEE), and must not be
disposed of as domestic garbage.
EU-wide legislation, as implemented in each Member State,
requires that waste electrical and electronic products carrying the
mark (left) must be disposed of separately from normal household
waste. This includes monitors and electrical accessories, such as
signal cables or power cords. When you need to dispose of your display
products, please follow the guidance of your local authority, or ask the shop
where you purchased the product. The mark on electrical and electronic
products only applies to the current European Union Member States.
Please follow the national guidelines for electrical and electronic product
disposal.
Classification
Power by Class I power supply (IEI, HTB-100-HM170)
No Applied Part.
No protection against the ingress of water: IPX0
Mode of operation: Continuous Operation
The equipment not suitable for use in the presence of a flammable
anesthetic mixture with air or with oxygen or nitrous oxide: Not AP or APG
Category.

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Contact Information
IEI Integration Corp.
Address: No. 29, Zongxing Rd., Xizhi Dist.,
New Taipei City 221, Taiwan
Phone:
[phone]
Fax:
[phone]
Web Site:
www.ieiworld.com
Sales Email:
[e-mail]