Order Catalog Implementation Guide
1.0.0-ballot - CI Build International flag

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

Example DeviceDefinition: Device model of presthetics-accessories

Page standards status: Informative

Language: en-US

Profile: Device Model

Reference to a catalog: Composition Worldwide Device Catalog

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

-MarketPeriodSubJurisdiction
*2019-05-05 --> (ongoing)urn:oid:2.16.840.1.113883.3.150

partNumber: P0-3.75,5

manufacturer: A.B. DENTAL DEVICES LTD

DeviceNames

-NameType
*Presthetic AccessoriesRegistered name

modelNumber: P0-3.75,5

classification

type: Dental implant suprastructure kit

Justifications

-TypeCitation
*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

classification

type: Dental implants - accessories

packaging

type: Bag, device

count: 10

UdiDeviceIdentifiers

-DeviceIdentifierIssuerJurisdiction
*17290107271407urn:oid:2.51.1.1urn:oid:2.16.840.1.113883.3.150

packaging

type: Bag, device

count: 100

UdiDeviceIdentifiers

-DeviceIdentifierIssuerJurisdiction
*27290107271404urn:oid:2.51.1.1urn:oid:2.16.840.1.113883.3.150

safety: Labeling does not Contain MRI Safety Information

languageCode: English (United States)

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:

Documents

-Url
*https://accessgudid.nlm.nih.gov/devices/07290107271400