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HT-F196UD 데이터시트(PDF) 3 Page - Inolux Corporation

부품명 HT-F196UD
상세설명  Harvatek Surface Mount LED
PDF  21 Pages
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제조업체  INOLUX [Inolux Corporation]
홈페이지  http://www.inolux-corp.com/index.php
Logo INOLUX - Inolux Corporation

HT-F196UD 데이터시트(HTML) 3 Page - Inolux Corporation

  HT-F196UD Datasheet HTML 1Page - Inolux Corporation HT-F196UD Datasheet HTML 2Page - Inolux Corporation HT-F196UD Datasheet HTML 3Page - Inolux Corporation HT-F196UD Datasheet HTML 4Page - Inolux Corporation HT-F196UD Datasheet HTML 5Page - Inolux Corporation HT-F196UD Datasheet HTML 6Page - Inolux Corporation HT-F196UD Datasheet HTML 7Page - Inolux Corporation HT-F196UD Datasheet HTML 8Page - Inolux Corporation HT-F196UD Datasheet HTML 9Page - Inolux Corporation Next Button
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HT-F196 Series
Official Product
Product: HT-F196 Series
Data Sheet No.
Tentative Product
****************
HT-F196 Series
Specifications are subject to change without notice. Data and
drawings herein are copyrighted.
June 23, 2013
Version of 1.0
Page
3/21
DISCLAIMER
HARVATEK reserves the right to make changes without further notice to any products herein
to improve reliability, function or design. HARVATEK does not assume any liability arising out
of the application or use of any product or circuit described herein; neither does it convey any
license under its patent rights, nor the rights of others.
LIFE SUPPORT POLICY
HARVATEK’s products are not authorized for use as critical components in life support devices
or systems without the express written approval of the President of HARVATEK or HARVATEK
INTERNATIONAL. As used herein:
1. Life support devices or systems are devices or systems which, (a) are intended for surgical
implant into the body, or (b) support or sustain life, and (c) whose failure to perform when
properly used in accordance with instructions for use provided in the labeling, can be
reasonably expected to result in a significant injury of the user.
2. A critical component in any component of a life support device or system whose failure to
perform can be reasonably expected to cause the failure of the life support device or system,
or to affect its safety or effectiveness.



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