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8 Infant Flow ® SiPAP<br />
Notices<br />
Copyright Notice<br />
Copyright © 2004 VIASYS Healthcare, Critical Care Division, California.<br />
This work is protected under Title 17 of the U.S. Code and is the sole property of the<br />
Company. No part of this document may be copied or otherwise reproduced, or<br />
stored in any electronic information retrieval system, except as specifically permitted<br />
under U.S. Copyright law, without the prior written consent of the Company. For<br />
more information, contact:<br />
World Headquarters European Office<br />
1100 Bird Center Drive Rembrandtlaan 1b<br />
Palm Springs, CA 92262-8099 3723 BG Bilthoven<br />
U.S.A. P.O. Box 299, 3720 AG Bilthoven<br />
Phone: (760) 778-7200 The Netherlands<br />
(800) 328-4139 Phone: +31 (30) 2289 711<br />
Fax: (760) 778-7274 Fax: +31 (30) 2286 244<br />
www.VIASYSCriticalCare.com<br />
Trademark Notices<br />
Infant Flow ® and SiPAP are trademarks of VIASYS Healthcare, Critical Care Division<br />
in the U.S. and some other countries. All other brand names and product names<br />
mentioned in this manual are trademarks, registered trademarks, or trade names of<br />
their respective holders.<br />
EMC Notice<br />
This equipment radiates and is susceptible to radio frequency energy. If not installed<br />
and used in accordance with the instructions in this manual, electromagnetic<br />
interference may result. The equipment has been tested and found to comply with<br />
the limits set forth in BS EN60601-1-2 for Medical Electrical Equipment Part 1-2:<br />
General requirements for safety-collateral standard. Electromagnetic compatibility –<br />
requirements and tests. These limits provide reasonable protection against<br />
electromagnetic interference when operated in the intended use environments (e.g.<br />
hospitals) described in this manual.<br />
This device is also designed and manufactured to comply with the following<br />
standards;<br />
Safety: UL 60601-1: 2003 Medical Electrical Equipment, Part 1: General<br />
Requirements for Safety.<br />
CAN/CSA C22.2 No 601.1-M90, Medical Electrical Equipment - Part<br />
1: General Requirements for Safety including C22.2 No. 601.1S1-94<br />
(IEC601-1, Amendment 1:1991) Supplement No. 1-94 to CAN/CSA<br />
22.2 No. 601.1-M90<br />
675-120 Revision C November 2004
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