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QBLP595-R5 データシート(PDF) 9 Page - QT-Brightek Corp.

部品番号 QBLP595-R5
部品情報  SMD 0402 Red LED
PDF  9 Pages
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メーカー  QTB [QT-Brightek Corp.]
ホームページ  https://www.qt-brightek.com/home.html
Logo QTB - QT-Brightek Corp.

QBLP595-R5 データシート(HTML) 9 Page - QT-Brightek Corp.

  QBLP595-R5 Datasheet HTML 1Page - QT-Brightek Corp. QBLP595-R5 Datasheet HTML 2Page - QT-Brightek Corp. QBLP595-R5 Datasheet HTML 3Page - QT-Brightek Corp. QBLP595-R5 Datasheet HTML 4Page - QT-Brightek Corp. QBLP595-R5 Datasheet HTML 5Page - QT-Brightek Corp. QBLP595-R5 Datasheet HTML 6Page - QT-Brightek Corp. QBLP595-R5 Datasheet HTML 7Page - QT-Brightek Corp. QBLP595-R5 Datasheet HTML 8Page - QT-Brightek Corp. QBLP595-R5 Datasheet HTML 9Page - QT-Brightek Corp.  
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QBLP595-R5
0402 LED
------------------------------------------------------------------------------------------------------------------------------------------
Product: QBLP595-R5
Date: July 20, 2022
Page 9 of 9
Version# 1.0
Revision History
Description:
Revision #
Revision Date
New Release of QBLP595-R5
V1.0
07/20/2022
Disclaimer
QT-BRIGHTEK reserves the right to make changes without further notice to any products herein to
improve reliability, function or design. QT-BRIGHTEK 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
QT-
BRIGHTEK’s products are not authorized for use as critical components in life support devices or
systems without the express written approval of QT-BRIGHTEK. 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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