Gunter,

did you ever figure this out? Should probably get corrected at a DICOM level, maybe CP.

On Tuesday, 10 July 2018 at 08:57:27 UTC-4, gunter zeilinger wrote:
> DICOM PS 3.3, A.45.2.3 Encapsulated CDA IOD Module Table ( http://dicom.nema.org/medical/dicom/current/output/html/part03.html#sect_A.45.2.3 ) lists Module SC Equipment as mandatory, which itself ( http://dicom.nema.org/medical/dicom/current/output/html/part03.html#sect_C.8.6.1 ) specifies Attribute Conversion Type (0008,0064) as Type 1, but actually none of the listed
>
> Defined Terms:
>
> DV
> Digitized Video
> DI
> Digital Interface
> DF
> Digitized Film
> WSD
> Workstation
> SD
> Scanned Document
> SI
> Scanned Image
> DRW
> Drawing
> SYN
> Synthetic Image
>
> does make much sense in case of an encapsulated CDA Document. Also the other optional (Type 3) attributes of Module SC Equipment
>
> Secondary Capture Device ID (0018,1010)
> Secondary Capture Device Manufacturer (0018,1016)
> Secondary Capture Device Manufacturer's Model Name (0018,1018)
> Secondary Capture Device Software Versions (0018,1019)
> Video Image Format Acquired (0018,1022)
> Digital Image Format Acquired (0018,1023)
>
> typically does not apply to encapsulated CDAs - except for CDAs which itself contain a captured image (e.g. image/jpeg) or a scanned document (e.g. application/pdf).
>
> So I would suggest to relax the requirements in Table A.45.2-1. Encapsulated CDA IOD Modules, by changing the Usage Type of the SC Equipment from M(andatory) to U(ser Option) or (C)onditional.
>
> Any thoughts?
>
> Gunter Zeilinger
> J4care