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 |
Implantable device/UDI example HIBBC Format (id = "example-udi3")
<Device xmlns="http://hl7.org/fhir"> <id value="example-udi3"/> <text> <status value="generated"/> <div xmlns="http://www.w3.org/1999/xhtml"><p> <b> Generated Narrative with Details</b> </p> <p> <b> id</b> : example-udi3</p> <p> <b> identifier</b> : Serial Number = XYZ456789012345678</p> <h3> Udis</h3> <table> <tr> <td> -</td> <td> <b> Name</b> </td> <td> <b> Jurisdiction</b> </td> <td> <b> CarrierHRF</b> </td> <td> <b> Issuer</b> </td> <td> <b> EntryType</b> </td> </tr> <tr> <td> *</td> <td> FHIR® Ulltra Implantable</td> <td> <a> http://hl7.org/fhir/NamingSystem/fda-udi</a> </td> <td> +H123PARTNO1234567890120/$$420020216LOT123456789012345/SXYZ456789012345678/16D20130202C</td> <td> <a> http://hl7.org/fhir/NamingSystem/hibcc</a> </td> <td> manual</td> </tr> </table> <p> <b> status</b> : inactive</p> <p> <b> lotNumber</b> : LOT123456789012345</p> <p> <b> manufacturer</b> : GlobalMed, Inc</p> <p> <b> manufactureDate</b> : 02/02/2013</p> <p> <b> expirationDate</b> : 02/02/2020</p> <p> <b> model</b> : Ultra Implantable</p> <p> <b> patient</b> : <a> Patient/example</a> </p> </div> </text> <identifier> <!-- The serial number which is a component of the production identifier (PI), a conditional, variable portion of a UDI. The identifier.type code should be set to “SNO”(Serial Number) and the system left empty. --> <type> <coding> <system value="http://hl7.org/fhir/identifier-type"/> <code value="SNO"/> </coding> </type> <value value="XYZ456789012345678"/> <!-- this is the serial number --> </identifier> <udi> <!-- brand name on label --> <name value="FHIR® Ulltra Implantable"/> <!-- This is US FDA example --> <jurisdiction value="http://hl7.org/fhir/NamingSystem/fda-udi"/> <!-- The Human readable form here which is FDA GS-1 format of the udi --> <carrierHRF value="+H123PARTNO1234567890120/$$420020216LOT123456789012345/SXYZ456789012345678/16D20130202C"/> <issuer value="http://hl7.org/fhir/NamingSystem/hibcc"/> <!-- YOu may want to know how the data was entered for data integrity reasons. This has overlap with Provenance which could identify the enterer --> <entryType value="manual"/> </udi> <status value="inactive"/> <lotNumber value="LOT123456789012345"/> <manufacturer value="GlobalMed, Inc"/> <manufactureDate value="2013-02-02"/> <!-- 20130202= this is the manufacturing date expressed in [YYYYMMDD] --> <expirationDate value="2020-02-02"/> <!-- 20020216 = this is the expiration date expressed in YYMMDDHH --> <model value="Ultra Implantable"/> <patient> <reference value="Patient/example"/> </patient> </Device>
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.