DICOM PS3.3 2018e - Information Object Definitions

A.37.3 Raw Data IOD Module Table (Current)
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### A.37.3 Raw Data IOD Module Table

Table A.37-1 specifies the Modules of the Raw Data IOD.

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.

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DICOM PS3.3 2018e - Information Object Definitions