Extensions for Using Data Elements from FHIR R5 in FHIR R4 - Downloaded Version null See the Directory of published versions

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: DeviceNameType - XML Representation

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<CodeSystem xmlns="http://hl7.org/fhir">
  <id value="device-nametype"/>
  <text>
    <status value="generated"/>
    <div xmlns="http://www.w3.org/1999/xhtml">
            <p>This 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-standards-status">
    <valueCode value="trial-use"/>
  </extension>
  <extension
             url="http://hl7.org/fhir/StructureDefinition/structuredefinition-fmm">
    <valueInteger value="1"/>
  </extension>
  <extension url="http://hl7.org/fhir/StructureDefinition/package-source">
    <extension url="packageId">
      <valueId value="hl7.fhir.uv.xver-r5.r4"/>
    </extension>
    <extension url="version">
      <valueString value="0.1.0"/>
    </extension>
    <extension url="uri">
      <valueUri
                value="http://hl7.org/fhir/uv/xver/ImplementationGuide/hl7.fhir.uv.xver-r5.r4"/>
    </extension>
  </extension>
  <extension
             url="http://hl7.org/fhir/StructureDefinition/structuredefinition-wg">
    <valueCode value="oo"/>
  </extension>
  <url value="http://hl7.org/fhir/device-nametype"/>
  <version value="5.0.0"/>
  <name value="DeviceNameType"/>
  <title value="Device Name Type"/>
  <status value="active"/>
  <experimental value="false"/>
  <date value="2021-01-04T17:01:24-06:00"/>
  <publisher value="Orders and Observations"/>
  <contact>
    <name value="Orders and Observations"/>
    <telecom>
      <system value="url"/>
      <value value="http://www.hl7.org/Special/committees/orders"/>
    </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|4.0.1"/>
  <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>