ClinicalDocument/informationRecipient MAY be present. When present, it SHALL be in
accordance with the HL7 CDA R2 standard and further constrained by this specification
to require the presence of name (on the informationRecipient and/or receivedOrganization),
addr and telecom. Additionally, it SHALL have the following:
<templateId root="1.3.6.1.4.1.19376.1.3.3.1.4"/> - The templateId element identifies
this participant as an intended recipient. The templateId SHALL have root="1.3.6.1.4.1.19376.1.3.3.1.4".
The informationRecipient/intendedRecipient element can be multiple. It introduces
an intended recipient of the laboratory report, other than the Ordering Provider (described
as a referrer participant). These elements carry the list of the originally intended
recipients of the laboratory report, i.e. those who were known at the time the report
was created and published for
sharing.
Context
Parent nodes van template element met id 1.3.6.1.4.1.19376.1.3.3.1.4
Classificatie
CDA header level template
Open/gesloten
Open (ook andere dan gedefinieerde elementen zijn toegestaan)
Gebruikt door / Gebruikt
Gebruikt door 0 transacties en 1 template, Gebruikt 2 templates