R6 Ballot (1st Draft)

This page is part of the FHIR Specification v6.0.0-ballot1: Release 6 Ballot (1st Draft) (see Ballot Notes). The current version is 5.0.0. For a full list of available versions, see the Directory of published versions

4.4.1.55 ValueSet http://hl7.org/fhir/ValueSet/device-nametype

Orders and Observations icon Work Group Maturity Level: 2Trial Use Use Context: Country: World, Not yet ready for Production use
Official URL: http://hl7.org/fhir/ValueSet/device-nametype Version: 6.0.0-ballot1
draft as of 2020-12-28 Computable Name: DeviceNameType
Flags: Experimental, Immutable OID: 2.16.840.1.113883.4.642.3.1083

This value set is used in the following places:

The type of name the device is referred by.


 

This expansion generated 18 Dec 2023


Expansion based on codesystem Device Name Type v6.0.0-ballot1 (CodeSystem)

This value set contains 3 concepts

CodeSystemDisplayDefinition
  registered-namehttp://hl7.org/fhir/device-nametypeRegistered name

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.

  user-friendly-namehttp://hl7.org/fhir/device-nametypeUser Friendly name

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.

  patient-reported-namehttp://hl7.org/fhir/device-nametypePatient Reported name

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.

 

See the full registry of value sets defined as part of FHIR.


Explanation of the columns that may appear on this page:

LvlA few code lists that FHIR defines are hierarchical - each code is assigned a level. For value sets, levels are mostly used to organize codes for user convenience, but may follow code system hierarchy - see Code System for further information
SourceThe source of the definition of the code (when the value set draws in codes defined elsewhere)
CodeThe code (used as the code in the resource instance). If the code is in italics, this indicates that the code is not selectable ('Abstract')
DisplayThe display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application
DefinitionAn explanation of the meaning of the concept
CommentsAdditional notes about how to use the code