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Example CodeSystem/device-nametype (XML)

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

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

Definition for Code SystemDeviceNameType

<?xml version="1.0" encoding="UTF-8"?>

<CodeSystem xmlns="http://hl7.org/fhir">
  <id value="device-nametype"/> 
  <meta> 
    <lastUpdated value="2024-06-14T04:47:47.285+00:00"/> 
    <profile value="http://hl7.org/fhir/StructureDefinition/shareablecodesystem"/> 
  </meta> 
  <text> 
    <status value="generated"/> 
    <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> 
  </text> 
  <extension url="http://hl7.org/fhir/StructureDefinition/structuredefinition-wg">
    <valueCode value="oo"/> 
  </extension> 
  <extension url="http://hl7.org/fhir/StructureDefinition/structuredefinition-standards-status">
    <valueCode value="trial-use"/> 
  </extension> 
  <extension url="http://hl7.org/fhir/StructureDefinition/structuredefinition-fmm">
    <valueInteger value="1"/> 
  </extension> 
  <url value="http://hl7.org/fhir/device-nametype"/> 
  <identifier> 
    <system value="urn:ietf:rfc:3986"/> 
    <value value="urn:oid:2.16.840.1.113883.4.642.4.1084"/> 
  </identifier> 
  <version value="6.0.0-cibuild"/> 
  <name value="DeviceNameType"/> 
  <title value="Device Name Type"/> 
  <status value="active"/> 
  <experimental value="false"/> 
  <date value="2021-01-05T10:01:24+11:00"/> 
  <publisher value="HL7 (FHIR Project)"/> 
  <contact> 
    <telecom> 
      <system value="url"/> 
      <value value="http://hl7.org/fhir"/> 
    </telecom> 
    <telecom> 
      <system value="email"/> 
      <value value="fhir@lists.hl7.org"/> 
    </telecom> 
  </contact> 
  <description value="The type of name the device is referred by."/> 
  <jurisdiction> 
    <coding> 
      <system value="http://unstats.un.org/unsd/methods/m49/m49.htm"/> 
      <code value="001"/> 
      <display value="World"/> 
    </coding> 
  </jurisdiction> 
  <caseSensitive value="true"/> 
  <valueSet value="http://hl7.org/fhir/ValueSet/device-nametype"/> 
  <content value="complete"/> 
  <concept> 
    <code value="registered-name"/> 
    <display value="Registered name"/> 
    <definition value="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."/> 
  </concept> 
  <concept> 
    <code value="user-friendly-name"/> 
    <display value="User Friendly name"/> 
    <definition value="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."/> 
  </concept> 
  <concept> 
    <code value="patient-reported-name"/> 
    <display value="Patient Reported name"/> 
    <definition value="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."/> 
  </concept> 
</CodeSystem> 

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.