Order Catalog Implementation Guide, published by HL7 International / Orders and Observations. This guide is not an authorized publication; it is the continuous build for version 1.0.0-ballot built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/fhir-order-catalog/ and changes regularly. See the Directory of published versions
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<DeviceDefinition xmlns="http://hl7.org/fhir">
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<div xmlns="http://www.w3.org/1999/xhtml" xml:lang="en-US" lang="en-US"><p class="res-header-id"><b>Generated Narrative: DeviceDefinition example-devicemodel-presthetics-accessories</b></p><a name="example-devicemodel-presthetics-accessories"> </a><a name="hcexample-devicemodel-presthetics-accessories"> </a><a name="example-devicemodel-presthetics-accessories-en-US"> </a><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">Language: en-US</p><p style="margin-bottom: 0px">Profile: <a href="StructureDefinition-DeviceModel.html">Device Model</a></p></div><p><b>Reference to a catalog</b>: <a href="Composition-example-device-catalog-header.html">Composition Worldwide Device Catalog</a></p><p><b>description</b>: </p><div><p>Titanium Healing Cap, 3.75 mm Diameter, 5 mm lengh</p>
</div><blockquote><p><b>udiDeviceIdentifier</b></p><p><b>deviceIdentifier</b>: 07290107271400</p><p><b>issuer</b>: urn:oid:2.51.1.1</p><p><b>jurisdiction</b>: urn:oid:2.16.840.1.113883.3.150</p><h3>MarketDistributions</h3><table class="grid"><tr><td style="display: none">-</td><td><b>MarketPeriod</b></td><td><b>SubJurisdiction</b></td></tr><tr><td style="display: none">*</td><td>2019-05-05 --> (ongoing)</td><td>urn:oid:2.16.840.1.113883.3.150</td></tr></table></blockquote><p><b>partNumber</b>: P0-3.75,5</p><p><b>manufacturer</b>: A.B. DENTAL DEVICES LTD</p><h3>DeviceNames</h3><table class="grid"><tr><td style="display: none">-</td><td><b>Name</b></td><td><b>Type</b></td></tr><tr><td style="display: none">*</td><td>Presthetic Accessories</td><td>Registered name</td></tr></table><p><b>modelNumber</b>: P0-3.75,5</p><blockquote><p><b>classification</b></p><p><b>type</b>: <span title="Codes:{http://terminology.hl7.org/CodeSystem/GMDN 44881}">Dental implant suprastructure kit</span></p><h3>Justifications</h3><table class="grid"><tr><td style="display: none">-</td><td><b>Type</b></td><td><b>Citation</b></td></tr><tr><td style="display: none">*</td><td>Citation</td><td><div><p>A collection of prefabricated dental devices and components used to create a suprastructure on a dental implant to mimic preparations of natural teeth. It is used during dental implant restorative and laboratory procedures and will typically consist of a direct dental abutment (the device that is screwed into the surgically implanted fixture that creates the anchorage for the prosthetic tooth in the mandible or maxilla), a carrier, an impression pick-up, a replica, a healing cap and a burnout cylinder. This is a single-use device.</p>
</div></td></tr></table></blockquote><blockquote><p><b>classification</b></p><p><b>type</b>: <span title="Codes:{http://snomed.info/sct 1141761008}">Dental implant suprastructure</span></p></blockquote><blockquote><p><b>classification</b></p><p><b>type</b>: <span title="Codes:{urn:oid:1.2.250.1.213.2.68 P01020180}">Dental implants - accessories</span></p></blockquote><blockquote><p><b>packaging</b></p><p><b>type</b>: <span title="Codes:{http://snomed.info/sct 37284003}">Bag, device</span></p><p><b>count</b>: 10</p><h3>UdiDeviceIdentifiers</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>17290107271407</td><td>urn:oid:2.51.1.1</td><td>urn:oid:2.16.840.1.113883.3.150</td></tr></table><blockquote><p><b>packaging</b></p><p><b>type</b>: <span title="Codes:{http://snomed.info/sct 37284003}">Bag, device</span></p><p><b>count</b>: 100</p><h3>UdiDeviceIdentifiers</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>27290107271404</td><td>urn:oid:2.51.1.1</td><td>urn:oid:2.16.840.1.113883.3.150</td></tr></table></blockquote></blockquote><p><b>safety</b>: <span title="Codes:{urn:oid:2.16.840.1.113883.3.26.1.1 C113844}">Labeling does not Contain MRI Safety Information</span></p><p><b>languageCode</b>: <span title="Codes:{urn:ietf:bcp:47 en-US}">English (United States)</span></p><blockquote><p><b>property</b></p><p><b>type</b>: <span title="Codes:">For single use</span></p><p><b>value</b>: true</p></blockquote><blockquote><p><b>property</b></p><p><b>type</b>: <span title="Codes:">Prescription use</span></p><p><b>value</b>: true</p></blockquote><blockquote><p><b>property</b></p><p><b>type</b>: <span title="Codes:">Over the counter</span></p><p><b>value</b>: false</p></blockquote><blockquote><p><b>property</b></p><p><b>type</b>: <span title="Codes:">Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)</span></p><p><b>value</b>: false</p></blockquote><blockquote><p><b>property</b></p><p><b>type</b>: <span title="Codes:">Device Packaged as Sterile</span></p><p><b>value</b>: false</p></blockquote><blockquote><p><b>property</b></p><p><b>type</b>: <span title="Codes:">Requires Sterilization Prior to Use</span></p><p><b>value</b>: true</p></blockquote><p><b>contact</b>: <a href="mailto:Info@ab-dent.com">Info@ab-dent.com</a></p><blockquote><p><b>guideline</b></p><blockquote><p><b>relatedArtifact</b></p><p><b>type</b>: Documentation</p><p><b>label</b>: Device described in GUDID:</p><h3>Documents</h3><table class="grid"><tr><td style="display: none">-</td><td><b>Url</b></td></tr><tr><td style="display: none">*</td><td><a href="https://accessgudid.nlm.nih.gov/devices/07290107271400">https://accessgudid.nlm.nih.gov/devices/07290107271400</a></td></tr></table></blockquote></blockquote></div>
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value="A collection of prefabricated dental devices and components used to create a suprastructure on a dental implant to mimic preparations of natural teeth. It is used during dental implant restorative and laboratory procedures and will typically consist of a direct dental abutment (the device that is screwed into the surgically implanted fixture that creates the anchorage for the prosthetic tooth in the mandible or maxilla), a carrier, an impression pick-up, a replica, a healing cap and a burnout cylinder. This is a single-use device."/>
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