DeviceDefinition FHIR Resource Proposal
- 1 DeviceDefinition
- 1.1 Owning Committee Name
- 1.2 Committee Approval Date:
- 1.3 Contributing or Reviewing Work Groups
- 1.4 FHIR Resource Development Project Insight ID
- 1.5 Scope of coverage
- 1.6 RIM scope
- 1.7 Resource appropriateness
- 1.8 Expected implementations
- 1.9 Content sources
- 1.10 Example Scenarios
- 1.11 Resource Relationships
- 1.12 Timelines
- 1.13 gForge Users
- 1.14 When Resource Proposal Is Complete
- 1.15 FMG Notes
Owning Committee Name
Orders & Observations
Committee Approval Date:
Please enter the date that the committee approved this Resource proposal
Contributing or Reviewing Work Groups
- Work Group Name
- or link
- or "None"
FHIR Resource Development Project Insight ID
Scope of coverage
This is a specialized resource that defines the characteristics and capabilities of a device. Devices include durable (reusable) medical equipment, implantable devices, as well as disposable equipment used for diagnostic, treatment and research for healthcare and public health, as well as devices such as an x-ray machine, lab analyzer, cellphone, computer, software/application, etc. A device may also be a simpler entity such as a syringe or applicator, provided with a medicinal product.
The DeviceDefinition resource is used to describe the common characteristics and capabilities of a device of a certain type or kind, e.g., a certain model or class of a device such as a x-ray model or personal wearable device model, whereas a Device resource documents an actual instance of a device such as the actual x-ray machine that is installed or the personal wearable device being worn
The DeviceDefinition is typically used in catalogs, publications, or other use cases where the reference to a device is generically to a type of device, not a specific instance of a device. For example, a catalog of orderable devices, or the mapping of device specific test codes and result values to industry standards.
There does not appear to be a DeviceDefinition concept in the RIM, rather only the Device instance is referenced The Common Product Model touches on elements, but not all.
The DeviceDefinition resource contains the "catalog" definition of a device - whether that definition is authored by the manufacturer or a regulatory entity and allows defining valid hierarchical device configurations (devices as part of other devices).
Device vs DeviceDefinition: The Device resource is meant to refer to a physical instance of a device - hence having attributes like lot number, patient, location and operational status, which the DeviceDefinition resource does not have.
Separating the DeviceDefinition from Device enables clearer distinction, considering that a number of use cases primarily focus on Device, while others focus on DeviceDefinition. There will be many more Device instances than there will be DeviceDefinition instances. The DeviceDefinition would be used in catalogs and would have a different update lifecycle to the Device resource instances.
Implementations of catalogs, e.g., LIVD as well as implementations needing to reference device definitions. The LIVD implementation guide addresses Lab device manufacturers to document recommended mapping of test codes and result values used on their devices using proprietary/local code systems to (inter)national vocabularies such as LOINC and SNOMED.
EMA plan to use this for representing the devices that are commonly supplied with medication items, within the same packaging (e.g., syringe, spoon etc). This "SPOR" project is currently implementing, with a first release in early 2020.
- HL7 FHIR Device and DeviceMetrics
- HL7 V2 EQU and DEV segments
- EMA XEVPRM implementation of regulatory medications information
Ordering supplies using SupplyRequest would typically reference DeviceDefinitions rather than specific devices.
Ordering DME would typically reference DeviceDefinitions rather than specific devices.
Standard vocabulary mappings for devices typically define common mappings based on device models, thus DeviceDefinition rather than for each individual device.
Submission by a pharmaceutical manufacturer of the details of a packaged medicinal product for licencing by regulators (e.g. EMA, FDA, MHRA) would typically include definitions of the devices included (description, dimensions, materials, manufacturer etc).
- PackagedMedicinalProductDefinition (contains devices as defined by DeviceDefinition)
September 2018 inclusion in FHIR R4.
Eric Haas, Jose Costa Teixeira
When Resource Proposal Is Complete
When you have completed your proposal, please send an email to FMGcontact@HL7.org