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HTLP912UB.YR 数据表(PDF) 2 Page - Inolux Corporation

部件名 HTLP912UB.YR
功能描述  International Lead Frame Axial Lamp
PDF  12 Pages
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制造商  INOLUX [Inolux Corporation]
网页  http://www.inolux-corp.com/index.php
标志 INOLUX - Inolux Corporation

HTLP912UB.YR 数据表(HTML) 2 Page - Inolux Corporation

  HTLP912UB.YR Datasheet HTML 1Page - Inolux Corporation HTLP912UB.YR Datasheet HTML 2Page - Inolux Corporation HTLP912UB.YR Datasheet HTML 3Page - Inolux Corporation HTLP912UB.YR Datasheet HTML 4Page - Inolux Corporation HTLP912UB.YR Datasheet HTML 5Page - Inolux Corporation HTLP912UB.YR Datasheet HTML 6Page - Inolux Corporation HTLP912UB.YR Datasheet HTML 7Page - Inolux Corporation HTLP912UB.YR Datasheet HTML 8Page - Inolux Corporation HTLP912UB.YR Datasheet HTML 9Page - Inolux Corporation Next Button
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HTLP912XXX Series
Axial
Through Hole Lamp
Official Product
HTLP912XXX series
Customer Part No.
Data Sheet No.
****************
****************
HTLP912XXX series
Specifications are subject to change without notice. Data and
drawings herein are copyrighted.
June 27, 2013
Version of 1.0
Page
2/12
DISCLAIMER
INOLUX reserves the right to make changes without further notice to any products herein to
improve reliability, function or design. INOLUX 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
INOLUX’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 INOLUX or INOLUX
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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