Onyx VENUS-191 Manuale utente
Mobile Cart Computer
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VENUS-221/191
22”/19” LCD with LED Backlight
Intel®N2800 Dual Core Processor
Mobile Cart Computer
User Guide
VENUS-221/VENUS-191 Manual 1st Ed
May, 2014
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Copyright Notice
This document is copyrighted, 2013. 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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Packing List
Before you begin installing your Mobile Cart Computer, please make
sure that the following items have been shipped:
VENUS191/221 Mobile Cart Computer
Medical power adaptor 150W/24V
Lithium batteries x2
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, USA Inc.
324 W. Blueridge Ave.,
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Orange, CA 92865, USA
Tel : +1-714-792-0774
Fax: +1-714-792-0481
Email: usasales@onyx-healthcare.com
usa.onyx-healthcare.com
Onyx Healthcare EUROPE B.V.
Ekkersrijt 4002, 5692 DA Son, The Netherlands
Tel : +31-(0)499-462020
Fax: +31-(0)499-462010
Email: eusales@onyx-healthcare.com
e-FAE@onyx-healthcare.com (RMA)
Onyx Healthcare Technology GmbH
An der Trift65d
63303 Dreieich , Germany
TEL: +49-(0)61033-7479-00
Fax: +49-(0)61033-7479-49
Email: eusales@onyx-healthcare.com
e-FAE@onyx-healthcare.com (RMA)
Onyx Healthcare (SU ZHOU) INC.
Room 12, 2F, Building B, No.5 Xing Han Street, Suzhou Industrial
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Park, Jiang Su Province, China
Tel: +86-512-67625700
Fax: +86-512-67617337
Email: cnsales@onyx-healthcare.com
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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 anyAC 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.
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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. 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
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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.
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Classification
1. Degree of production against electric shock: not classified
2. Degree of protection against the ingress of water: Front IP65 and
body IPX1
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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