| DESCRIPTION |
+---------------------------------------------------------------+
| a medical device. As such, it may not be changed in any way. |
| Modifications to this software may result in an adulterated |
| medical device under 21CFR820, the use of which is considered |
| to be a violation of US Federal Statutes. |
+---------------------------------------------------------------+
The purpose of this table is to specify the first groups
of digits for the unique object identifiers that will be
generated by the software.
Note that this "root" for the UIDs is organization-specific,
| Property of the US Government. |
and that the FOIA release of this software will only
include data for this table for VA sites.
See the DICOM Standard (www.nema.org/dicom) PS 3.8 Annex A
for instructions on how to obtain a valid UID root.
| No permission to copy or redistribute this software is given. |
| Use of unreleased versions of this software requires the user |
| to execute a written test agreement with the VistA Imaging |
| Development Office of the Department of Veterans Affairs, |
| telephone (301) 734-0100. |
| |
| The Food and Drug Administration classifies this software as |
|
