
ONYX-MD116
11.6” LCD with LED Backlight
Intel® Apollo Lake processor
Dual smart card readers for multiple-care workflow
Instant vehicle docking system
Mobile Medical Assistant
ONYX-MD116 Manual 1st Ed
November, 2017

Copyright Notice
This document is copyrighted, 2017. 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

Acknowledgments
Intel
®
PentiumTM is registered trademarks of Intel® Corporation.
Microsoft
®
Windows is a registered trademark of Microsoft®
Corporation.
All other product names or trademarks are properties of their
respective owners.

Packing List
Before you begin installing your Mobile Medical Assistant, please
make sure that the following items have been shipped:
ONYX-MD116 Mobile Medical Assistant
ONYX-MD116 Docking Station(model: OPM-T016)
Four VESA Screws(M:4mm x P:0.7mm x L:10mm)

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, Lane 235, Pao-Chiao Rd.,
Hsin-Tien City, Taipei 231, Taiwan, R.O.C.
TEL: +886-2-8919-2188
FAX: +886-2-8919-1699
E-mail: sales@onyx-healthcare.com
http://www.onyx-healthcare.com
Worldwide Offices:
Onyx Healthcare Inc.
2F., No.135, Ln. 235, Baoqiao Rd., Xindian Dist.,
New Taipei City 231, Taiwan (R.O.C.)
TEL: +886-2-8919-2188
FAX: +886-2-8919-1699
E-mail: sales@onyx-healthcare.com
http://www.onyx-healthcare.com
Worldwide Offices:
Onyx Healthcare, USA Inc.
324W. Blueridge Ave., Orange,, CA 92865, USA
Tel : +1-714-792-0774
Fax: +1-714-792-0481

Email: usasales@onyx-healthcare.com
Onyx Healthcare EUROPE B.V.
Primulalaan 42, 5582 GL Waalre, Netherlands
Tel : +31-(0)499-745600
Email: eusales@onyx-healthcare.com
Onyx Healthcare (Shanghai) INC.
20F, unit D, GEM Building, No. 487 Tianlin Road,
Shanghai, China
Tel: +86-021-64956588
Fax: +86-021-64956889
Email: cnsales@onyx-healthcare.com

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. Warning: To avoid risk of electric shock, this equipment must
only be connected to a supply mains with protective earth.
(Avertissement: Pour éviter tout risque de choc électrique, cet
appareil doit être connecté à une alimentation secteur avec une
prise de terre)
10. Position the power cord so that people cannot step on it. Do
not place anything over the power cord.
11. All cautions and warnings on the equipment should be noted.

12. If the equipment is not used for a long time, disconnect it from
the power source to avoid damage by transient over-voltage.
13. Never pour any liquid into an opening. This could cause fire or
electrical shock.
14. Never open the equipment. For safety reasons, only qualified
service personnel should open the equipment.
15. Warning: Do not modify this equipment without authorization of
the manufacturer. (Avertissement: Ne pas modifier cet équipement
sans l'autorisation du fabricant)
16. Warning : It is necessary for checking or replacing the battery
pack every year. (Avertissement: Il est nécessaire de vérifier ou de
remplacer la batterie chaque année)

16. 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 users manual.
e. The equipment has been dropped and damaged.
f. The equipment has obvious signs of breakage.
17. 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.
18. External equipment intended for connection to signal
input/output or other connectors, shall comply with
relevant UL / IEC standard (e.g. UL 1950 for IT equipment
and ANSI/AAMI ES 60601-1: 2005 AND CAN/CSA-C22.2 No.
60601-1:08 / IEC 60601 series for systems – shall comply
with the standard IEC 60601-1-1, Safety requirements for
medical electrical systems. Equipment not complying
with UL 60601-1 shall be kept outside the patient
environment, as defined in the standard.
Caution:
It may cause the danger of explosion if battery is incorrectly
replaced. Replace only with same or equivalent type
recommended by the manufacturer.

Classification
1. Degree of production against electric shock: not classified
2. Degree of protection against the ingress of water: IPX0
3. Mode of operation: Continuous
4. Type of protection against electric shock: Class I equipment
5. No Applied Part, No AP/APG

FCC
This device complies with Part 18 FCC
Rules. 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.

ONYX-MD116 module is developed to
suitable for the Classification Mark
requirement
OPM-T016 module is developed to suitable for
the Classification Mark requirement