Adverse Event Clinical Research R4 Backport
1.0.1 - STU1 International flag

This page is part of the Adverse Event Clinical Research R4 Backport (v1.0.1: STU 1) based on FHIR (HL7® FHIR® Standard) R4. This is the current published version. For a full list of available versions, see the Directory of published versions

: Device - Infuser that exploded - XML Representation

Page standards status: Informative

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<Device xmlns="http://hl7.org/fhir">
  <id value="device-infuser"/>
  <text>
    <status value="generated"/>
    <div xmlns="http://www.w3.org/1999/xhtml"><p><b>Generated Narrative: Device</b><a name="device-infuser"> </a><a name="hcdevice-infuser"> </a></p><div style="display: inline-block; background-color: #d9e0e7; padding: 6px; margin: 4px; border: 1px solid #8da1b4; border-radius: 5px; line-height: 60%"><p style="margin-bottom: 0px">Resource Device &quot;device-infuser&quot; </p></div><p><b>identifier</b>: /10896128002012</p><h3>UdiCarriers</h3><table class="grid"><tr><td style="display: none">-</td><td><b>DeviceIdentifier</b></td><td><b>Issuer</b></td><td><b>Jurisdiction</b></td></tr><tr><td style="display: none">*</td><td>10896128002012</td><td><a href="http://hl7.org/fhir/NamingSystem/hibcc-dI">http://hl7.org/fhir/NamingSystem/hibcc-dI</a></td><td><a href="http://hl7.org/fhir/NamingSystem/fda-udi">http://hl7.org/fhir/NamingSystem/fda-udi</a></td></tr></table><p><b>status</b>: inactive</p><p><b>manufacturer</b>: Safe Device Co</p><p><b>manufactureDate</b>: 2000-02-01</p><p><b>expirationDate</b>: 2021-02-01</p><p><b>serialNumber</b>: C7H5N3O6</p><blockquote><p><b>deviceName</b></p><p><b>name</b>: Hyperspeed</p><p><b>type</b>: manufacturer-name</p></blockquote><blockquote><p><b>deviceName</b></p><p><b>name</b>: Hyperspeed Chemo Infuser</p><p><b>type</b>: user-friendly-name</p></blockquote><p><b>modelNumber</b>: FRN</p><p><b>type</b>: Infusion Pump <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> ()</span></p><p><b>owner</b>: <span>: Place that owns the device</span></p><p><b>location</b>: <span>: Where device is found</span></p></div>
  </text>
  <identifier>
    <type>
      <coding>
        <system value="http://hl7.org/fhir/NamingSystem/hibcc-dI"/>
      </coding>
    </type>
    <value value="10896128002012"/>
  </identifier>
  <udiCarrier>
    <deviceIdentifier value="10896128002012"/>
    <issuer value="http://hl7.org/fhir/NamingSystem/hibcc-dI"/>
    <jurisdiction value="http://hl7.org/fhir/NamingSystem/fda-udi"/>
  </udiCarrier>
  <status value="inactive"/>
  <manufacturer value="Safe Device Co"/>
  <manufactureDate value="2000-02-01"/>
  <expirationDate value="2021-02-01"/>
  <serialNumber value="C7H5N3O6"/>
  <deviceName>
    <name value="Hyperspeed"/>
    <type value="manufacturer-name"/>
  </deviceName>
  <deviceName>
    <name value="Hyperspeed Chemo Infuser"/>
    <type value="user-friendly-name"/>
  </deviceName>
  <modelNumber value="FRN"/>
  <type>
    <text value="Infusion Pump"/>
  </type>
  <owner>
    <display value="Place that owns the device"/>
  </owner>
  <location>
    <display value="Where device is found"/>
  </location>
</Device>