Onyx MD-100Pro User Manual

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MD-100Pro

10.1” Mini Bedside Terminal

SAMSUNG S5PV210 1GHz Processor

Ultra Low Power Consumption

Fanless & Compact design

MD-100Pro Manual 1st Edition

Dec, 2012

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Copyright Notice

This document is copyrighted, 2012. All rights are reserved. The
original manufacturer reserves the right to make improvements to
the products described in this manual at any time without notice.

No part of this manual may be reproduced, copied, translated, or
transmitted in any form or by any means without the prior written
permission of the original manufacturer. Information provided in
this manual is intended to be accurate and reliable. However, the
original manufacturer assumes no responsibility for its use, nor
for any infringements upon the rights of third parties, which may
result from its use.

The material in this document is for product information only and
is subject to change without notice. While reasonable efforts have
been made in the preparation of this document to assure its
accuracy, ONYX Healthcare Inc., assumes no liabilities resulting
from errors or omissions in this document, or from the use of the
information contained herein

ONYX Healthcare Inc. reserves the right to make changes in the
product design without notice to its users

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Acknowledgments

 SAMSUNG S5PV210 1GHz Process are registered

trademarks of SAMSUNG.

 IBM, PC/AT, PS/2 are trademarks of International Business

Machines Corporation.

 Microsoft

®

Windows is a registered trademark of Microsoft ®

Corporation.

 RTL is a trademark of Realtek Semi-Conductor Co., Ltd.
 C&T is a trademark of Chips and Technologies, Inc.
 UMC is a trademark of United Microelectronics Corporation.
 ITE is a trademark of Integrated Technology Express, Inc.
 SiS is a trademark of Silicon Integrated Systems Corp.
 VIA is a trademark of VIA Technology, Inc.

All other product names or trademarks are properties of their
respective owners.

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Packing List

Before you begin installing your Bedside Terminal, please make
sure that the following items have been shipped:

 MD-100Pro Mobile Tablet PC.
 AC/DC adapter and AC power cord
 Utility CD-ROM (Please insert the MD-100Pro CD-ROM into

external CD-ROM drive.), Drivers and Utilities

If any of these items are missing or damaged, you should contact
your distributor or sales representative immediately.

Headquarters
Onyx Healthcare Inc.
2F., No.135, Ln. 235, Baoqiao Rd., Xindian Dist.,
New Taipei City 231, Taiwan (R.O.C.).
TEL: [phone]
FAX: [phone]
E-mail: [e-mail]
http://www.onyx-healthcare.com

Worldwide Offices:

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Onyx Healthcare, USA Inc.
2663 Saturn street, Brea, CA 92821, USA
Tel : [phone]
Fax: [phone]
Email: [e-mail]

Onyx Healthcare EUROPE B.V.
Ekkersrijt 4002, 5692 DA Son, The Netherlands
Tel : [phone]
Fax: [phone]
Email: [e-mail]

Onyx Healthcare Technology GmbH
An der Trift65d
63303 Dreieich , Germany
TEL: [phone]
Fax: [phone]
Email: [e-mail]

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Onyx Healthcare (Nanjing) INC.
Room 1318, Metallurgy Building , East Zhongshan Road,
Nanjing, China
Tel: [phone]
Fax: [phone]
Email: [e-mail]

Onyx Healthcare Singapore PTE LTD
57 Genting Lane, #07-00, Singapore 349564
Tel: [phone]
Fax [phone]
Email: [e-mail]

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Safety & Warranty

1. Read these safety instructions carefully.

2. Keep this user's manual for later reference.

3. Disconnect this equipment from any AC outlet before cleaning. Do

not use liquid or spray detergents for cleaning. Use a damp cloth.

4. For pluggable equipment, the power outlet must be installed near the

equipment and must be easily accessible.

5. Keep this equipment away from humidity.

6. Put this equipment on a reliable surface during installation. Dropping

it or letting it fall could cause damage.

7. The openings on the enclosure are for air convection. Protect the

equipment from overheating. DO NOT COVER THE OPENINGS.

8. Make sure the voltage of the power source is correct before

connecting the equipment to the power outlet.

9. Position the power cord so that people cannot step on it. Do not

place anything over the power cord.

10. All cautions and warnings on the equipment should be noted.

11. If the equipment is not used for a long time, disconnect it from the

power source to avoid damage by transient over-voltage.

12. Never pour any liquid into an opening. This could cause fire or

electrical shock.

13. Never open the equipment. For safety reasons, only qualified service

personnel should open the equipment.

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14. If any of the following situations arises, get the equipment checked

by service personnel:

a. The power cord or plug is damaged.
b. Liquid has penetrated into the equipment.
c. The equipment has been exposed to moisture.
d. The equipment does not work well, or you cannot get it to

work according to the user’s manual.
e. The equipment has been dropped and damaged.
f. The equipment has obvious signs of breakage.

15. 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). IT MAY DAMAGE
THE EQUIPMENT.

16. External equipment intended for connection to signal

input/output or other connectors, shall comply with relevant UL
/ IEC standard (e.g. UL 60950-1 for IT equipment and ANSI/AAMI
ES 60601-1 / IEC 60601-1 series for systems – shall comply with
the standard IEC 60601-1-1, Safety requirements for medical
electrical systems. Equipment not complying with ANSI/AAMI
ES 60601-1 shall be kept outside the patient environment, as
defined in the standard.

17. WARNING: To avoid the risk of electric shock, this equipment

must only be connected to supply mains with protective earth.

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18. “ WARNING: No modification of this equipment is allowed”

19. Replaceable Batteries: The equipment contains replaceable
lithium battery, user replaceable type: The following warning in
user manual and service instructions.

* Caution: Danger of explosion if battery is incorrectly

replaced. Replace only with the same or equivalent type of battery
recommended by the manufacturer. Dispose of used batteries
according to the manufacturer instruction.

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Classification

1. Degree of production against electric shock: not classified

2. Equipment not suitable for use in the presence of a flammable

anesthetic mixture with air or with oxygen or nitrous oxide.

3. Mode of operation: Continuous

4. Type of protection against electric shock: Class I equipment

5. ME EQUIPMENT must be connected to an appropriate power

source, if loss of the power source would result in an
unacceptable RISK.

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Regulations Information

FCC-B Radio Frequency Interference Statement

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 in a residential installation. This equipment
generates, uses and radiates 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.

 Consult the dealer or an experienced radio TV technician for

help.