The Raw Data Information Object Definition (IOD) specifies raw data.
The E-R Model in Section A.1.2 depicts those components of the DICOM Information Model, which directly reference the Raw Data IOD.
Table A.37-1. Raw Data IOD Modules
IE |
Module |
Reference |
Usage |
---|---|---|---|
Patient |
Patient |
M |
|
Clinical Trial Subject |
U |
||
Study |
General Study |
M |
|
Patient Study |
U |
||
Clinical Trial Study |
U |
||
Series |
General Series |
M |
|
Clinical Trial Series |
U |
||
Frame of Reference |
Frame of Reference |
U |
|
Synchronization |
C - Required if time synchronization was applied. |
||
Equipment |
General Equipment |
M |
|
Raw Data |
Acquisition Context |
M |
|
Specimen |
U |
||
Raw Data |
M |
||
SOP Common |
M |
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.