DICOM PS3.3 2016a - Information Object Definitions
A.37.3 Raw Data IOD Module Table
Prev  A.37 Raw Data IOD  Next
PS3.3 > Composite Information Object Definitions (Normative) > Raw Data IOD > Raw Data IOD Module Table

A.37.3 Raw Data IOD Module Table

Table A.37-1. Raw Data IOD Modules

IE

Module

Reference

Usage

Patient

Patient

C.7.1.1

M

Clinical Trial Subject

C.7.1.3

U

Study

General Study

C.7.2.1

M

Patient Study

C.7.2.2

U

Clinical Trial Study

C.7.2.3

U

Series

General Series

C.7.3.1

M

Clinical Trial Series

C.7.3.2

U

Frame of Reference

Frame of Reference

C.7.4.1

U

Synchronization

C.7.4.2

C - Required if time synchronization was applied.

Equipment

General Equipment

C.7.5.1

M

Raw Data

Acquisition Context

C.7.6.14

M

Specimen

C.7.6.22

U

Raw Data

C.19.1

M

SOP Common

C.12.1

M

Note

The Specimen Identification Module was previously included in this IOD but has been retired, and its functionality replaced by the Specimen Module. See PS3.3-2008.

Prev  Up  Next
A.37.2 Raw Data Entity-Relationship Model  Home  A.38 Enhanced Computed Tomography Image IOD
DICOM PS3.3 2016a - Information Object Definitions