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ref Template  Participant (Body, device)

Id 2.16.756.5.30.1.1.10.4.10
ref
(from repository: ch-palm-)		 Effective Date valid from 2017‑03‑24 16:17:11
Status draft Draft Version Label 2017
Name chpalm_entry_ParticipantBodyDevice Display Name Participant (Body, device)
Description Declaration of analyzer, test kit and manufacturer used to determine the result.
All participating elements (including devices), MUST according to XD-LAB contain name, addr and telecom.
Classification CDA Entry Level Template
Open/Closed Open (other than defined elements are allowed)
Used by / Uses
Used by 0 transactions and 8 templates, Uses 1 template
Used by as Name Version
2.16.756.5.30.1.1.10.4.17 Containment draft Laboratory Isolate Organizer (2017) 2017‑03‑24 16:26:22
2.16.756.5.30.1.1.10.4.4 link draft Laboratory Report Data Processing Entry (2017) 2017‑03‑21 10:41:01
2.16.756.5.30.1.1.10.3.3 link draft Laboratory Speciality Section (2017) 2017‑03‑16 23:57:18
2.16.756.5.30.1.1.1.1.3.9.1 link draft Laboratory Report V1 (2017) 2016‑03‑23
2.16.756.5.30.1.1.10.3.5 link draft Laboratory Report Item Section (2017) 2017‑03‑20 21:27:50
2.16.756.5.30.1.1.10.4.19 Containment draft Laboratory Battery Organizer (2017) 2017‑03‑24 16:28:35
2.16.756.5.30.1.1.10.4.3 Containment draft Laboratory Observation (2017) 2017‑03‑21 10:38:18
notice Circular reference found with 2.16.756.5.30.1.1.10.4.3, please check
2.16.756.5.30.1.1.10.4.11 link draft Specimen Collection (2017) 2017‑03‑24 16:18:41
Uses as Name Version
2.16.756.5.30.1.1.10.9.21 Containment draft Device with Name (2017) DYNAMIC
Relationship Specialization: template 2.16.840.1.113883.10.12.321 (2005‑09‑07)
Specialization: template 1.3.6.1.4.1.19376.1.3.1.9999.10.9.11 (2016‑07‑05)
Item DT Card Conf Description Label
@typeCode
 cs 1 … 1 F DEV
hl7:participantRole
 1 … 1 R (chpalm_entry_ParticipantBodyDevice)
hl7:playingDevice
 1 … 1 R Analyzer used to determine the result.
Contains 2.16.756.5.30.1.1.10.9.21 Device with Name (DYNAMIC) 		(chpalm_entry_ParticipantBodyDevice)
hl7:scopingEntity
 0 … 1 The test kit and its manufacturer CAN be specified. (chpalm_entry_ParticipantBodyDevice)
hl7:id
 II 0 … * The number of the test kit with which the result was determined CAN be specified. Multiple numbers are PERMITTED. (chpalm_entry_ParticipantBodyDevice)
@extension
 st 1 … 1 R MUST contain the number itself. The number MUST be unique within the system that issued the number.
@root
 uid 1 … 1 R MUST contain the OID of the system that issued the ID. OIDs of code systems, which are published in the public OID registry for the Swiss health care system (oid.refdata.ch) are REQUIRED. Others are NOT ALLOWED.
hl7:code
 CE 0 … 1 A code that identifies the test kit CAN be specified.
If no vocabulary is available, nullFlavor='ASKU' including a displayName MUST be used. In this case, @code, @codeSystem and @codeSystemName are NOT ALLOWED.
TODO schematron to check these busines rules. 		(chpalm_entry_ParticipantBodyDevice)
@nullFlavor
 cs 0 … 1 F ASKU
  If no vocabulary is available, nullFlavor='ASKU' including a displayName MUST be used.
@displayName
 st 1 … 1 R Name of the test kit, as used in the narrative text.
@codeSystemName
 st 0 … 1   The name of the code system MUST be specified for tracking purposes. However, processing is NOT ALLOWED.
@codeSystem
 oid 0 … 1   The OID of the code system MUST be specified.
@code
 cs 0 … 1   The code MUST be specified.
hl7:desc
 ED 0 … 1 The manufacturer (name) of the test kit and any further information MAY be declared. (chpalm_entry_ParticipantBodyDevice)