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Packagehl7.terminology
Resource TypeCodeSystem
IdCodeSystem-device-nametype.json
FHIR VersionR5
Sourcehttps://build.fhir.org/ig/HL7/UTG/CodeSystem-device-nametype.html
URLhttp://terminology.hl7.org/CodeSystem/device-nametype
Version1.0.0
Statusactive
Date2026-06-01
NameDeviceNameType
TitleDevice Name Type
Realmuv
Authorityhl7
DescriptionThe type of name the device is referred by.
CopyrightThis material derives from the HL7 Terminology (THO). THO is copyright ©1989+ Health Level Seven International and is made available under the CC0 designation. For more licensing information see: https://terminology.hl7.org/license
Contentcomplete

Resources that use this resource

ValueSet
hl7.terminology#currentdevice-nametypeDevice Name Type

Resources that this resource uses

No resources found


Narrative

Note: links and images are rebased to the (stated) source

Generated Narrative: CodeSystem device-nametype

Last updated: 2026-05-28 22:17:06+0000

This case-sensitive code system http://terminology.hl7.org/CodeSystem/device-nametype defines the following codes:

CodeDisplayDefinition
registered-name Registered nameThe term assigned to a device by the entity that may be registered or submitted to a jurisdiction, certification body, or its databases. This may be considered the manufacturer assigned name (e.g., brand name assigned by the labeler or manufacturer in US, or device name assigned by the manufacturer in EU) and may also be synonymous with proprietary name or trade name of the device.
user-friendly-name User Friendly nameThe term that generically describes the device by a name as assigned by the manufacturer that is recognized by lay person. This common or generic name may be printed on the package it came in or some combination of that name with the model number, serial number, or other attribute that makes the name easy to understand for the user of that device. It is often exposed in communicating devices transport protocols. It is provided to help users identify the device when reported in discovery operations.
patient-reported-name Patient Reported namethe term used by the patient associated with the device when describing the device, for example 'knee implant', when documented as a self-reported device.

Source1

{
  "resourceType": "CodeSystem",
  "id": "device-nametype",
  "meta": {
    "lastUpdated": "2026-05-28T22:17:06.96+00:00"
  },
  "text": {
    "status": "generated",
    "div": "<!-- snip (see above) -->"
  },
  "extension": [
    {
      "url": "http://hl7.org/fhir/StructureDefinition/structuredefinition-wg",
      "valueCode": "oo"
    },
    {
      "url": "http://hl7.org/fhir/StructureDefinition/structuredefinition-fmm",
      "valueInteger": 2
    }
  ],
  "url": "http://terminology.hl7.org/CodeSystem/device-nametype",
  "identifier": [
    {
      "system": "urn:ietf:rfc:3986",
      "value": "urn:oid:2.16.840.1.113883.4.642.4.1084"
    }
  ],
  "version": "1.0.0",
  "name": "DeviceNameType",
  "title": "Device Name Type",
  "status": "active",
  "experimental": false,
  "date": "2026-06-01",
  "publisher": "Health Level Seven International",
  "contact": [
    {
      "telecom": [
        {
          "system": "url",
          "value": "http://hl7.org"
        },
        {
          "system": "email",
          "value": "hq@HL7.org"
        }
      ]
    }
  ],
  "description": "The type of name the device is referred by.",
  "jurisdiction": [
    {
      "coding": [
        {
          "system": "http://unstats.un.org/unsd/methods/m49/m49.htm",
          "code": "001",
          "display": "World"
        }
      ]
    }
  ],
  "copyright": "This material derives from the HL7 Terminology (THO). THO is copyright ©1989+ Health Level Seven International and is made available under the CC0 designation. For more licensing information see: https://terminology.hl7.org/license",
  "caseSensitive": true,
  "valueSet": "http://terminology.hl7.org/ValueSet/device-nametype",
  "content": "complete",
  "concept": [
    {
      "code": "registered-name",
      "display": "Registered name",
      "definition": "The term assigned to a device by the entity that may be registered or submitted to a jurisdiction, certification body, or its databases. This may be considered the manufacturer assigned name (e.g., brand name assigned by the labeler or manufacturer in US, or device name assigned by the manufacturer in EU) and may also be synonymous with proprietary name or trade name of the device."
    },
    {
      "code": "user-friendly-name",
      "display": "User Friendly name",
      "definition": "The term that generically describes the device by a name as assigned by the manufacturer that is recognized by lay person.  This common or generic name may be printed on the package it came in or some combination of that name with the model number, serial number, or other attribute that makes the name easy to understand for the user of that device. It is often exposed in communicating devices transport protocols. It is provided to help users identify the device when reported in discovery operations."
    },
    {
      "code": "patient-reported-name",
      "display": "Patient Reported name",
      "definition": "the term used by the patient associated with the device when describing the device, for example 'knee implant', when documented as a self-reported device."
    }
  ]
}