Onyx MD101 User Manual

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Main model: ONYX-MD101

Series Model: xxxONYX-MD101xxxxxxxxxx(x=0~9, A~Z,

a~z or blank or middle bar; for marketing purpose only and no

impact safety related constructions and critical components)

10.1” LCD with LED Backlight

Intel® Cherry Trail Z8350 Processor

Mobile Medical Assistant Tablet

ONYX-MD101 Manual 1st Ed

Jul, 2017

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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

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Acknowledgments

 Intel

®

Cherry Trail 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 respec
tive owners.

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Packing List

Before you begin installing your Medical Tablet PC, please make sure
that the following items have been shipped:

 ONYX-MD101 Mobile Medical Assistant Tablet
 Medical Power Adapter 15V/2.4A
 Utility DVD-ROM, which contains Drivers and Utilities
 VESA Cradle (Optional)

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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: [phone]
FAX: [phone]
E-mail: [e-mail]
http://www.onyx-healthcare.com

Worldwide Offices:
Onyx Healthcare, USA Inc.
324W. Blueridge Ave., Orange,, CA 92865, USA
Tel : [phone]
Fax: [phone]
Email: [e-mail]

Onyx Healthcare EUROPE B.V.
Primulalaan 42, 5582 GL Waalre, Netherlands
Tel : [phone]
Email: [e-mail]

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Onyx Healthcare (Shanghai) INC.
20F, unit D, GEM Building, No. 487 Tianlin Road,
Shanghai, China
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. 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.

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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)

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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.

19. Unplug the power cord from the power adapter jack to
disconnect the device.

Caution:

It may cause the danger of explosion if battery is incorrectly
replaced. Replace only with same or equivalent type
recommended by the manufacturer.

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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

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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.

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UL Module Description

ONYX-MD101 modules are developed to
suitable for the Classification Mark
requirement

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Safety Symbol Description

The following safety symbols are the further explanations for your
reference.

Medical equipment with respect to electric
shock, fire and mechanical hazards only in
accordance with ANSI/AAMI ES 60601-1:

2005 AND CAN/CSA-C22.2 No.
60601-1:08

Attention, consult ACCOMPANYING
DOCUMENTS.

Stand-by

Ground wire
Protective Ground wire.

Alternating current

Direct current