R4 Ballot #1 (Mixed Normative/Trial use)

This page is part of the FHIR Specification (v3.3.0: R4 Ballot 2). 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

Device-example-udi1

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-udi1

identifier: 1234-5678-90AB-CDEF, Serial Number = 10987654d321

Udis

-

DeviceIdentifier

Name

Jurisdiction

CarrierHRF

CarrierAIDC

Issuer

EntryType

*

00844588003288

FHIR® Hip System

http://hl7.org/fhir/NamingSystem/fda-udi

{01}00844588003288{17}141120{10}7654321D{21}10987654d321

XWQyMDExMDg1NzY3NDAwMjAxNzE3MTQxMTIwMTBOWUZVTDAx4oaUMjExOTI4MzfihpQ3MTNBMUIyQzNENEU1RjZH

http://hl7.org/fhir/NamingSystem/gs1

barcode

status: active

type: Coated femoral stem prosthesis, modular (Details : {SNOMED CT code '468063009' = 'Coated femoral stem prosthesis, modular', given as 'Coated femoral stem prosthesis, modular'})

lotNumber: 7654321D

manufacturer: Acme Devices, Inc

expirationDate: 20/11/2014

model: PM/Octane 2014

patient: Patient/example

safety: MR Unsafe (Details : {urn:oid:2.16.840.1.113883.3.26.1.1 code 'mr-unsafe' = 'mr-unsafe', given as 'MR Unsafe'})

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.