Order Catalog Implementation Guide, published by HL7 International - Orders and Observations Work Group. This is not an authorized publication; it is the continuous build for version current). 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
Generated Narrative: DeviceDefinition
Resource DeviceDefinition "example-devicemodel-presthetics-accessories" (Language "en-US")
Profile: Device Model
Reference to a catalog: Composition/example-device-catalog-header
description: Titanium Healing Cap, 3.75 mm Diameter, 5 mm lengh
udiDeviceIdentifier
deviceIdentifier: 07290107271400
issuer:
urn:oid:2.51.1.1
jurisdiction:
urn:oid:2.16.840.1.113883.3.150
MarketDistributions
MarketPeriod SubJurisdiction 2019-05-05 --> (ongoing) urn:oid:2.16.840.1.113883.3.150
partNumber: P0-3.75,5
manufacturer: : A.B. DENTAL DEVICES LTD
Name | Type |
Presthetic Accessories | registered-name |
modelNumber: P0-3.75,5
classification
type: Dental implant suprastructure kit (Global Medical Device Nomenclature#44881)
Justifications
Type Citation citation 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.
classification
type: Dental implant suprastructure (SNOMED CT#1141761008)
classification
type: Dental implants - accessories (unknown#P01020180)
packaging
type: Bag, device (SNOMED CT#37284003)
count: 10
UdiDeviceIdentifiers
DeviceIdentifier Issuer Jurisdiction 17290107271407 urn:oid:2.51.1.1
urn:oid:2.16.840.1.113883.3.150
packaging
type: Bag, device (SNOMED CT#37284003)
count: 100
udiDeviceIdentifier
safety: Labeling does not Contain MRI Safety Information (unknown#C113844)
languageCode: American English (ISO 639-1: Codes for the representation of names of languages -- Part 1: Alpha-2 code#en-US)
property
type: For single use ()
value: true
property
type: Prescription use ()
value: true
property
type: Over the counter ()
value: false
property
type: Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P) ()
value: false
property
type: Device Packaged as Sterile ()
value: false
property
type: Requires Sterilization Prior to Use ()
value: true
contact: Info@ab-dent.com
guideline
relatedArtifact
type: documentation
label: Device described in GUDID:
document