R6 Ballot (1st Draft)

This page is part of the FHIR Specification v6.0.0-ballot1: Release 6 Ballot (1st Draft) (see Ballot Notes). The current version is 5.0.0. For a full list of available versions, see the Directory of published versions

Example CodeSystem/device-nametype (JSON)

Orders and Observations Work GroupMaturity Level: N/AStandards Status: Informative

Raw JSON (canonical form + also see JSON Format Specification)

Definition for Code SystemDeviceNameType

{
  "resourceType" : "CodeSystem",
  "id" : "device-nametype",
  "meta" : {
    "lastUpdated" : "2023-12-18T15:12:07.602+11:00",
    "profile" : ["http://hl7.org/fhir/StructureDefinition/shareablecodesystem"]
  },
  "text" : {
    "status" : "generated",
    "div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p>This case-sensitive code system <code>http://hl7.org/fhir/device-nametype</code> defines the following codes:</p><table class=\"codes\"><tr><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td><td><b>Definition</b></td></tr><tr><td style=\"white-space:nowrap\">registered-name<a name=\"device-nametype-registered-name\"> </a></td><td>Registered name</td><td>The term assigned to a medical device by the entity who registers or submits information about it to a jurisdiction 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.</td></tr><tr><td style=\"white-space:nowrap\">user-friendly-name<a name=\"device-nametype-user-friendly-name\"> </a></td><td>User Friendly name</td><td>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.</td></tr><tr><td style=\"white-space:nowrap\">patient-reported-name<a name=\"device-nametype-patient-reported-name\"> </a></td><td>Patient Reported name</td><td>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.</td></tr></table></div>"
  },
  "extension" : [{
    "url" : "http://hl7.org/fhir/StructureDefinition/structuredefinition-wg",
    "valueCode" : "oo"
  },
  {
    "url" : "http://hl7.org/fhir/StructureDefinition/structuredefinition-standards-status",
    "valueCode" : "trial-use"
  },
  {
    "url" : "http://hl7.org/fhir/StructureDefinition/structuredefinition-fmm",
    "valueInteger" : 1
  }],
  "url" : "http://hl7.org/fhir/device-nametype",
  "identifier" : [{
    "system" : "urn:ietf:rfc:3986",
    "value" : "urn:oid:2.16.840.1.113883.4.642.4.1084"
  }],
  "version" : "6.0.0-ballot1",
  "name" : "DeviceNameType",
  "title" : "Device Name Type",
  "status" : "active",
  "experimental" : false,
  "date" : "2021-01-05T10:01:24+11:00",
  "publisher" : "HL7 (FHIR Project)",
  "contact" : [{
    "telecom" : [{
      "system" : "url",
      "value" : "http://hl7.org/fhir"
    },
    {
      "system" : "email",
      "value" : "fhir@lists.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"
    }]
  }],
  "caseSensitive" : true,
  "valueSet" : "http://hl7.org/fhir/ValueSet/device-nametype",
  "content" : "complete",
  "concept" : [{
    "code" : "registered-name",
    "display" : "Registered name",
    "definition" : "The term assigned to a medical device by the entity who registers or submits information about it to a jurisdiction 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."
  }]
}

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.