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Template XeH Lab Device Participant 2022‑07‑30 14:57:58

Id2.16.840.1.113883.2.51.10.91Effective Date2022‑07‑30 14:57:58
Statusactive ActiveVersion Label1.0
NameXeHLabDeviceParticipantDisplay NameXeH Lab Device Participant
ClassificationCDA Header Level Template
Open/ClosedOpen (other than defined elements are allowed)
Used by / Uses
Used by 0 transactions and 4 templates, Uses 0 templates
Used by as NameVersion
2.16.840.1.113883.2.51.10.36Includeactive XeH Laboratory Report Data Processing Entry (1.0)2021‑10‑07 00:14:07
2.16.840.1.113883.2.51.10.56Includeactive XeH Laboratory Observation (1.0)2022‑02‑16 15:03:27
2.16.840.1.113883.2.51.10.70Includeactive XeH Laboratory Battery Organizer (2017)2022‑05‑09 22:33:51
2.16.840.1.113883.2.51.10.92Includeactive XeH Laboratory Isolate Organizer (1.0)2022‑07‑31 07:54:30
ItemDTCardConfDescriptionLabel
hl7:participantRole
1 … 1MXeHLdotspant
hl7:id
II0 … *The UDI Device Identifier MAY be specified as a second id element.
XeHLdotspant
hl7:playingDevice
1 … 1MXeHLdotspant
hl7:code
CE.IPS0 … 1Coded product type
XeHLdotspant
hl7:manufacturerModelName
SC0 … 1The element manufacturerModelName“ is intended to be used in the same manner as element “modelNumber” specified in the FHIR device resource. It shall carry model information of the device or software provided in element softwareName
XeHLdotspant
hl7:softwareName
SC1 … 1M
The element softwareName is the primary element and intended to be used in the same manner as element “deviceName” specified in the FHIR device resource. It should carry the name of the device or software.

Is SHOULD including the manufacturer name.

Note: In case of usage for laboratory related documentation (e.g. Laboratory Result Report), the device structure is also used to record "Laboratory Kits" used for the examination.
XeHLdotspant