Standard Practice for Digital Imaging and Communication in Nondestructive Evaluation (DICONDE) for Ultrasonic Test Methods
|Publication Date:||1 December 2011|
This practice facilitates the interoperability of ultrasonic
imaging equipment by specifying image data transfer and archival
storage methods in commonly accepted terms. This document is
intended to be used in conjunction with Practice E2339 on Digital
Imaging and Communication in Nondestructive Evaluation (DICONDE).
Practice E2339 defines an industrial adaptation of the NEMA
Standards Publication titled Digital Imaging and Communications in
Medicine (DICOM, see http://medical.nema.
This practice has been developed to overcome the issues that arise when analyzing or archiving data from ultrasonic test equipment using proprietary data transfer and storage methods. As digital technologies evolve, data must remain decipherable through the use of open, industry-wide methods for data transfer and archival storage. This practice defines a method where all the ultrasonic technique parameters and test results are communicated and stored in a standard format regardless of changes in digital technology.
This practice does not specify:
A testing or validation procedure to assess an implementation's conformance to the standard.
The implementation details of any features of the standard on a device claiming conformance.
The overall set of features and functions to be expected from a system implemented by integrating a group of devices each claiming DICONDE conformance.
Although this practice contains no values that require units, it does describe methods to store and communicate data that do require units to be properly interpreted. The SI units required by this practice are to be regarded as standard. No other units of measurement are included in this standard.
This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.
*A Summary of Changes section appears at the end of this standard.