HM-JACKarc Operation Manual
Introduction
1 - 2
Rev.4
Applicable laws and standards
This Analyzer falls under a medical analyzer as specified by the
Pharmaceutical Affairs Act of Japan.
Medical instrument manufacturing license number: 22B3X00004
With regard to the electrical safety test, this is a Class I device of Type
B as specified by JIS T1001 and IEC 61010-1, 2.
Caution
This Manual should be kept where it will be readily available to those
who use this Analyzer.
The content of this Manual and software is subject to change without
notice.
In the event of any inconsistencies between this document and the
software, the software is to take precedence.
All other company names and product names used in this Manual
are trademarks or registered trademarks of their respective
companies.
Reproduction of all or part of this Manual without prior consent is
prohibited.
The content of this Manual is subject to change without notice.
While we have taken all possible precautions to ensure quality in the
content of this Manual, please contact your dealership or contact Kyowa
Medex Co., Ltd. if you find anything unclear, or any apparent errors or
omissions. Our contact details are stated on the last page of this
Manual.
This Manual is copyrighted by Kyowa Medex Co., Ltd.
2005 Kyowa Medex Co., Ltd. All Rights Reserved
Restrictions
Copying of the
HM-JACKarc
application software without prior
consent is prohibited.
We do not warrant the functionality of the
HM-JACKarc
control
computer when used for other purposes.
Do not install any other application software on the
HM-JACKarc
control computer. We do not warrant the functionality of the PC if any
other applications are installed.
Do not start any other application while the
HM-JACKarc
application
is running. We do not warrant the functionality if any other
application is running at the same time.
We do not warrant measurement data that is accidentally deleted.
Password-based restriction is provided for functions that are not
required in normal operation.
