SMART Product Catalog
0.1.0 - ci-build
SMART Product Catalog, published by WHO. This guide is not an authorized publication; it is the continuous build for version 0.1.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/WorldHealthOrganization/smart-pcmt/tree/draft-logical-model and changes regularly. See the Directory of published versions
| Official URL: http://smart.who.int/pcmt/ValueSet/NameType | Version: 0.1.0 | |||
| Draft as of 2025-01-31 | Computable Name: NameType | |||
Product name type
References
Generated Narrative: ValueSet NameType
http://hl7.org/fhir/device-nametype
Generated Narrative: ValueSet
Expansion done internally based on codesystem Device Name Type v5.0.0 (CodeSystem)
This value set contains 3 concepts
| Code | System | Display | Definition |
| registered-name | http://hl7.org/fhir/device-nametype | Registered 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-name | http://hl7.org/fhir/device-nametype | User 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-name | http://hl7.org/fhir/device-nametype | Patient 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. |
Explanation of the columns that may appear on this page:
| Level | A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies |
| System | The source of the definition of the code (when the value set draws in codes defined elsewhere) |
| Code | The code (used as the code in the resource instance) |
| Display | The 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 |
| Definition | An explanation of the meaning of the concept |
| Comments | Additional notes about how to use the code |