DICOM Conformance Statement

DICOM Conformance Statement for Cerner ProVision TM PACS Release 4.5
Columns 0028,0011 S,*,U
Bits Allocated 0028,0100 S,*,U
Bits Stored 0028,0101 S,*,U
Observation DateTime 0040,A032 NONE
Completion Flag 0040,A491 NONE
Completion Flag Description 0040,A492 NONE
Verification Flag 0040,A493 NONE
Content Label 0070,0080 NONE
Content Description 0070,0081 NONE
Presentation Creation Date 0070,0082 NONE
Presentation Creation Time 0070,0083 NONE
Content Creator’s Name 0070,0084 NONE
Table 21: Patient Root Supported Elements
Name Tag Types of Matching
STUDY Level
Study Date 0008,0020 S,*,U,R
Study Time 0008,0030 S,*,U,R
Accession Number 0008,0050 S,*,U
Modalities in Study 0008,0061 S,*,U,R
Referring Physician Name 0008,0090 S,*,U
Study Description 0008,1030 S,*,U
Patient Name 0010,0010 S,*,U
Patient ID 0010,0020 S,*,U,L
Study Instance UID 0020,000D UNIQUE,L
Study ID 0020,0010 S,*,U
Number of Study Related Series 0020,1206 NONE
Number of Study Related Instances 0020,1208 NONE
SERIES Level
Series Date 0008,0021 S,*,U,R
Series Time 0008,0031 S,*,U,R
Retrieve AE Title 0008,0054 NONE
Modality 0008,0060 S,*,U,L
Manufacturer 0008,0070 NONE
Station Name 0008,1010 NONE
Series Description 0008,103E S,*,U
Body Part Examined 0018,0015 S,*,U
Patient Position 0018,5100 S,*,U
View Position 0018,5101 S,*,U
Series Instance UID 0020,000E UNIQUE,L
Series Number 0020,0011 S,*,U
Laterality 0020,0016 S,*,U
Cerner Corporation February 27, 2007 Page 24