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Andigilog, Inc. 
8380 S. Kyrene Rd., Suite 101 
Tempe, Arizona 85284 
Tel: (480) 940-6200      
Fax: (480) 940-4255 
 Andigilog, Inc. 2006 
- 40 - 
www.andigilog.com
October 2006 - 70A05007 
aSC7611
Data Sheet Classifications 
Preliminary Specification 
This classification is shown on the heading of each page of a specification for products that are either under 
development (design and qualification), or in the formative planning stages.  Andigilog reserves the right to 
change or discontinue these products without notice. 
New Release Specification 
This classification is shown on the heading of the first page only of a specification for products that are either 
under the later stages of development (characterization and qualification), or in the early weeks of release to 
production.  Andigilog reserves the right to change the specification and information for these products without 
notice. 
Fully Released Specification 
Fully released datasheets do not contain any classification in the first page header. These documents contain 
specification on products that are in full production. Andigilog will not change any guaranteed limits without 
written notice to the customers.  Obsolete datasheets that were written prior to January 1, 2001 without any 
header classification information should be considered as obsolete and non-active specifications, or in the best 
case as Preliminary Specifications. 
Pentium is a trademark of Intel Corporation 
Athlon and Duron are trademarks of AMD Corporation 
Windows XP is a trademark of Microsoft Corporation 
LIFE SUPPORT POLICY 
ANDIGILOG'S PRODUCTS ARE NOT AUTHORIZED FOR USE AS CRITICAL COMPONENTS IN LIFE SUPPORT DEVICES 
OR SYSTEMS WITHOUT THE EXPRESS WRITTEN APPROVAL OF THE PRESIDENT AND GENERAL COUNSEL OF 
ANDIGILOG, INC.  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 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 to the user.  
2.  A critical component is 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.