Uzbekistan Digital Health Platform
0.12.0 - ci-build Uzbekistan flag

Uzbekistan Digital Health Platform, published by Ministry of Health of the Republic of Uzbekistan. This guide is not an authorized publication; it is the continuous build for version 0.12.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/uzinfocom-org/digital-health-ig/ and changes regularly. See the Directory of published versions

ValueSet: Device name type (Experimental)

Official URL: https://terminology.dhp.uz/fhir/core/ValueSet/device-name-type-vs Version: 0.12.0
Draft as of 2026-10-30 Computable Name: DeviceNameTypeVS

Device name types

References

Logical Definition (CLD)

This ValueSet requires the Code system Supplement Device name type translations.

 

Expansion

This value set contains 3 concepts

SystemCodeDisplay (en)DefinitionJSONXML
http://hl7.org/fhir/device-nametype  registered-nameRegistered nameThe 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.
http://hl7.org/fhir/device-nametype  user-friendly-nameUser Friendly nameThe 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.
http://hl7.org/fhir/device-nametype  patient-reported-namePatient Reported namethe term used by the patient associated with the device when describing the device, for example 'knee implant', when documented as a self-reported device.

Description of the above table(s).