FHIR to OMOP FHIR IG, published by HL7 International / Biomedical Research and Regulation. 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/HL7/fhir-omop-ig/ and changes regularly. See the Directory of published versions
Official URL: http://hl7.org/fhir/uv/omop/StructureDefinition/DeviceExposure | Version: 0.1.0 | |||
Standards status: Draft | Maturity Level: 1 | Computable Name: DeviceExposure |
The Device domain captures information about a person's exposure to a foreign physical object or instrument which is used for diagnostic or therapeutic purposes through a mechanism beyond chemical action. Devices include implantable objects (e.g. pacemakers, stents, artificial joints), medical equipment and supplies (e.g. bandages, crutches, syringes), other instruments used in medical procedures (e.g. sutures, defibrillators) and material used in clinical care (e.g. adhesives, body material, dental material, surgical material).).
Usage:
Description of Profiles, Differentials, Snapshots and how the different presentations work.
This structure is derived from Base
This structure is derived from Base
Summary
Mandatory: 0 element(5 nested mandatory elements)
Structures
This structure refers to these other structures:
Maturity: 1
Differential View
This structure is derived from Base
Key Elements View
Snapshot View
This structure is derived from Base
Summary
Mandatory: 0 element(5 nested mandatory elements)
Structures
This structure refers to these other structures:
Maturity: 1