This page is part of the FHIR Specification (v3.0.2: STU 3). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions . Page versions: R5 R3
Orders and Observations Work Group | Maturity Level: N/A | Ballot Status: Informative | Compartments: Device |
This is the narrative for the resource. See also the XML or JSON format. This example conforms to the profile Device.
Generated Narrative with Details
id: example-udi2
- | DeviceIdentifier | Name | Jurisdiction | Issuer |
* | A9999XYZ100T0474 | Bone,Putty Demineralized | http://hl7.org/fhir/NamingSystem/fda-udi | http://hl7.org/fhir/NamingSystem/iccbba-other |
status: inactive
manufacturer: Acme Devices, Inc
manufactureDate: 01/02/2013
expirationDate: 01/02/2014
patient: Patient/example
Usage note: every effort has been made to ensure that the examples are correct and useful, but they are not a normative part of the specification.