Device (53)

#NameSourceVerDescription
1ADHA Implantable Medical Deviceau.digitalhealth.r4#currentR4The purpose of this profile is to define a representation of an implantable medical device for a patient for exchange usage scenarios to support the electronic exchange of health information between individuals, healthcare providers, and the My Health Record system infrastructure in Australia.
2ADHA Participant Deviceau.digitalhealth.r4#currentR4The purpose of this profile is to define a representation of a device acting as an observer or performer for exchange usage scenarios to support the electronic exchange of health information between individuals, healthcare providers, and the My Health Record system infrastructure in Australia.
3ADHA System Deviceau.digitalhealth.r4#currentR4The purpose of this profile is to define a representation of a device as a system in the role of an author or exchange target or source for exchange usage scenarios to support the electronic exchange of health information between individuals, healthcare providers, and the My Health Record system infrastructure in Australia.
4Argonaut Device Profilefhir.argonaut.r2#1.0.0R2
5AS Device Profileans.fhir.fr.annuaire#1.0.0-ballot-2R4Profil créé à partir de Device dans le contexte de l'Annuaire Santé pour décrire les équipements matériels lourds ('EML') mis en oeuvre au sein d'un établissement.
6AS Donnée Publique Device Profileans.fhir.fr.annuaire#1.0.0-ballot-2R4Profil applicatif créé à partir du profil générique as-device dans le contexte des données en libre accès de l’Annuaire Santé.
7AS Donnée Restreinte Device Profileans.fhir.fr.annuaire#1.0.0-ballot-2R4Profil applicatif créé à partir du profil générique as-device dans le contexte des données en accès restreint de l’Annuaire Santé.
8AU Core System Devicehl7.fhir.au.core#currentR4This profile sets minimum expectations for a Device resource to record, search, and fetch basic identifying and other administrative information about an information system device. It is based on the core [Device]( http://hl7.org/fhir/R4/device.html) resource and identifies the *additional* mandatory core elements, extensions, vocabularies and value sets that **SHALL** be present in the Device when conforming to this profile. It provides the floor for standards development for specific uses cases in an Australian context.
9Blood Pressure Devicehl7.fhir.us.vitals#currentR4A profile of the Device resource used specifically for blood pressure devices and includes an extension for blood pressure cuff size.
10CH EMED EPR Devicech.cara.fhir.epr.emed#currentR4Definition of the device for the eMedication context
11CH eTOC Devicech.fhir.ig.ch-etoc#currentR4Definition for the Device resource in the context of electronic transition of care.
12Channel Device profilehl7.fhir.uv.pocd#currentR4StructureDefinition for Device resources that represent Channels, which are used for grouping metrics together.
13CMI Software System Devicehl7.fhir.uv.cmi#currentR4The Software System device profile is used to capture software details about the various systems used in authoring, testing, packaging, or evaluation of a knowledge artifact
14CQFM Devicehl7.fhir.us.cqfmeasures#currentR4The SoftwareSystem device profile is used to capture software details about the various systems used in authoring, testing, packaging, or evaluation of a knowledge artifact
15CRD Devicehl7.fhir.us.davinci-crd#currentR4This profile specifies additional constraints on the US Core Device Profile to support coverage requirements discovery.
16CRMI Software System Devicehl7.fhir.uv.crmi#currentR4The Software System device profile is used to capture software details about the various systems used in authoring, testing, packaging, or evaluation of a knowledge artifact
17Device (AU IPS)hl7.fhir.au.ips#currentR4This profile is based on the UV profile, with Australian rules added as well (by reference to the Australian profile)
18Device (CZ)ncez.cz.fhir.core#currentR4This profile represents the constraints applied to the Device resource by the Czech national interoperability project.
19Device (IPS)hl7.fhir.uv.ips#currentR4This profile represents the constraints applied to the Device resource by the International Patient Summary (IPS) FHIR Implementation Guide, based on FHIR R4. A device used by or implanted on the patient is described in the patient summary as an instance of a Device resource constrained by this profile.
20Device - At-Home In-Vitro Testhl7.fhir.us.home-lab-report#currentR4This profile constrains the Device resource for At-Home In-Vitro Tests.
21Device - DICOM SR TID 4019 Algorithm Identification Mappinghl7.fhir.uv.dicom-sr#currentR5DICOM SR Algorithm Identification to Device
22Device - Lab Reporthl7.fhir.it.lab-report#currentR4Descrive la risorsa Device che descrive un dispositivo.
23Device - performer, observerhl7.fhir.au.ips#currentR4This profile is based on the UV profile, with Australian rules added as well (by reference to the Australian profile)
24Device - performer, observerhl7.fhir.uv.ips#currentR4This profile represents the constraints applied to the Device resource by the IPS project, which specifies an international patient summary based on the FHIR standard R4.; This profile describes a device that plays the role of observer or performer.
25Device - performer, observerncez.cz.fhir.core#currentR4This profile represents the constraints applied to the Device resource by the Czech national interoperability project. This profile describes a device that plays the role of observer or performer.
26Device CRNhl7.fhir.us.womens-health-registries#0.2.0R4Device profile for CRN project
27Device Profile (Implantable)hl7.fhir.ca.baseline#currentR4Proposed constraints on the Device resource for the minimal set of data to query and retrieve a patient's implantable device.
28Device Profile (Medical and Non-medical)hl7.fhir.ca.baseline#currentR4Proposed constraints on the Device resource for the minimal set of data to query and retrieve a medical or non-medical device.
29Finnish PHR Device profileSUPPORT.R4#3.0.0R4Finnish PHR profile device. Used in vital sign observations.
30HCIM AbilityToPerformMouthcareActivities MedicalDeviceProductnictiz.fhir.nl.stu3.zib2017#2.2.15R3A MedicalDeviceProduct resource as defined by the Dutch Health and Care Information models (Dutch: Zorginformatiebouwsteen or ZIB) AbilityToPerformMouthcareActivities v3.1(2017EN). The ability to perform mouthcare activities is part of self-care. This includes brushing teeth twice a day with fluoride toothpaste and/or cleaning (partial) dentures, cleaning jaws without teeth (edentulous jaws) and taking care of the mucous membrane of the mouth. Limitations in this ability indicate a reduced ability to cope for oneself. This activity and activities such as those including eating, getting dressed and bathing are also known as activities of daily living (ADL). These are the activities people go through in daily life. The extent to which a person is able to do all these activities by themselves is a measure for their total ability to do things independently. (Source: Instruction card for oral hygiene, 2011)
31HCIM BladderFunction UrineCatheter Productnictiz.fhir.nl.stu3.zib2017#2.2.15R3Resource describes what product is used as an urine catheter.
32HCIM FeedingTubeSystem Productnictiz.fhir.nl.stu3.zib2017#2.2.15R3This resource is part of FeedingTubeSystem as defined by the Dutch Health and Care Information models (Dutch: Zorginformatiebouwsteen or ZIB) version 3.2, release 2017.
33HCIM HearingFunction HearingAid Productnictiz.fhir.nl.stu3.zib2017#2.2.15R3A HearingFunction resource as defined by the Dutch Health and Care Information models (Dutch: Zorginformatiebouwsteen or ZIB) HearingFunction v3.1(2017EN). Hearing is the ability to observe sound, with the purpose of communicating with others, localizing the source of the sound and recognizing certain sounds. This pertains to observing the sound waves, and not processing the sounds in the brain. A hearing disorder can lead to things including communication problems.
34HCIM Infusion Productnictiz.fhir.nl.stu3.zib2017#2.2.15R3This resource is part of Infusion as defined by the Dutch Health and Care Information models (Dutch: Zorginformatiebouwsteen or ZIB) version 3.2, release 2017.
35HCIM MedicalDevice Productnictiz.fhir.nl.stu3.zib2017#2.2.15R3This resource is part of MedicalDevice as defined by the Dutch Health and Care Information models (Dutch: Zorginformatiebouwsteen or ZIB) version 3.1, release 2017. Medical aids are any internally implanted and external devices and/or aids used by the patient (in the past) to reduce the effects of functional limitations in organ systems or to facilitate the treatment of a disease.
36HCIM Respiration AdministeredOxygen AdministrationDeviceProductnictiz.fhir.nl.stu3.zib2017#2.2.15R3A Device resource as defined by the Dutch HCIM Respiration v3.1(2017EN). During breathing or respiration, air flows to and from the lungs, where gas exchange occurs, absorbing oxygen from the air into the blood and exhaling carbon dioxide into the air. Observations of spontaneous breathing, usually registered as part of the observation of vital functions.
37HCIM VisualFunction VisualAid Productnictiz.fhir.nl.stu3.zib2017#2.2.15R3An Observation resource as defined by the Dutch Health and Care Information models (Dutch: Zorginformatiebouwsteen or ZIB) VisualFunction v3.1(2017EN). Sight is the ability to observe lit objects, with the goal of orienting yourself on objects and people in a lit environment. This pertains to observing the light stimuli, and not processing them in the brain. A sight disorder can lead to things including orientation problems.
38HCIM Wound MedicalDeviceProductnictiz.fhir.nl.stu3.zib2017#2.2.15R3A deviceUseStatement as defined by the Dutch HCIM Zorginformatiebouwsteen Wond v3.1(2017EN). A drain is a medical aid placed to drain blood and exudate from the wound area.
39Imaging Devicearkhn.fhir.uv.osiris#currentR4Qualification of the equipment used to acquire a series of images
40MDS Device profilehl7.fhir.uv.pocd#currentR4StructureDefinition for Device resources that represent a Medical Device System (MDS). This is the top-level resource in the hierarchical model of a Point-of-Care device.
41MedNet Interface (MNI) - Deviceswiss.mednet.fhir#0.15.0R4MedNet Interface (MNI) - Device Profile
42mHealth ADE Device profilehl7.fhir.uv.mhealth-framework#0.1.0R4Defines constraints on the Device Resource for data communicating about the source of device data.
43Modality Devicehl7.fhir.uv.radiation-dose-summary#currentR4Modality profiling as a Device resource
44PDex Devicehl7.fhir.us.davinci-pdex#currentR4The PDex Device profile is provided to enable payers to record information about devices used by a member that may not have a UDI number. FHIR-29796 PDex Device uses base resource not US Core Implantable Device Profile. Pdex-Device enables payers to record non-implantable device data. CGP Voted on variance approval: Drew Torres/Eric Haas: 9-0-0
45PhdDevicehl7.fhir.uv.phd#currentR4Base StructureDefinition for the Device Resource for a PHD
46PhgDevicehl7.fhir.uv.phd#currentR4Base StructureDefinition for the Device Resource for a PHG
47QICore Devicehl7.fhir.us.qicore#currentR4Profile of Device for decision support/quality metrics. Defines the core set of elements and extensions for quality rule and measure authors.
48Radiotherapy Seed Devicehl7.fhir.us.codex-radiation-therapy#currentR4A device that represents implanted seeds for brachytherapy. The device is specified by the type of radioactive seed (at a minimum).
49Radiotherapy Treatment Devicehl7.fhir.us.codex-radiation-therapy#currentR4The device used to deliver radiotherapy. For example, a LINAC (external beam) or an afterloader (brachytherapy). The device is specified by at least its manufacturer and model name.
50RTLS Tag Device Profilehl7.fhir.uv.rtls#currentR5Device resource profile for tags or badges in RTLS workflows.
51Sequencing Devicearkhn.fhir.uv.osiris#currentR4Description of a sequencing device used for a Sequencing Analysis.
52US Core Implantable Device Profilehl7.fhir.us.core#currentR4The US Core Implantable Device Profile is based upon the core FHIR Device Resource and meets the U.S. Core Data for Interoperability (USCDI) v2 *Unique Device Identifier(s) for a Patient's Implantable Device(s)* requirements. To promote interoperability and adoption through common implementation, this profile sets minimum expectations for the Device resource to record, search, and fetch UDI information associated with a patient's implantable device(s). It identifies which core elements, extensions, vocabularies, and value sets **SHALL** be present in the resource and constrains the way the elements are used when using this profile. It provides the floor for standards development for specific use cases.
53VMD Device profilehl7.fhir.uv.pocd#currentR4StructureDefinition for Device resources that represent Virtual Medical Devices (VMD). These are medical-related subsystems in the hierarchical model of a Point-of-Care device.
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Device I C D D D I D D D D D D D I D D D
Device.id D
Device.specialization C C D C D D
Device.specialization.version C D
Device.specialization.systemType C D
Device.specialization.systemType.coding S C (2) S C (2)
Device.specialization.systemType.coding.code C C
Device.specialization.systemType.coding.system C F C F
Device.distinctIdentifier C C C C C
Device.statusReason C C D C
Device.udi C
Device.udi.carrierHRF D
Device.udi.deviceIdentifier
Device.deviceName C C C C C S C (2) C D C S C (3) S C (2)
Device.deviceName.type C F C F C F F B M F F F (2) F
Device.deviceName.name C C C
Device.patient C I C C C D C C C C C C C C C C
Device.patient.reference C C
Device.meta C C
Device.meta.profile C F S C F (2) S C F (2)
Device.meta.tag D
Device.meta.security D
Device.meta.source D
Device.meta.lastUpdated D
Device.meta.versionId D
Device.meta.extension S C D
Device.implicitRules C D
Device.language
Device.text
Device.contained
Device.extension S C (3) S C (2) S C D (4) S C D (6) S C D (5)
Device.extension.valueCode
Device.extension.valueCodeableConcept
Device.extension.valueCodeableConcept.coding
Device.extension.valueCodeableConcept.coding.code
Device.extension.valueCodeableConcept.coding.system
Device.extension.valueUnsignedInt (2) (2) (2)
Device.extension.extension S (2) S (2)
Device.extension.extension.valueString
Device.extension.extension.valueUnsignedInt
Device.modifierExtension C D
Device.identifier S C (2) S C (2) C S C (3) C S C D (2) S C (2) S C (5) S C D (4) S C D (4) C C D
Device.identifier.use D
Device.identifier.value C (3) C D C C C (4) C D (3) C D (3)
Device.identifier.system C F (3) C D C F F C F D (3) C F D (3)
Device.identifier.assigner D C
Device.identifier.period D C
Device.identifier.type D C C F C F (4) C (3) C (3)
Device.identifier.type.coding C C (3) C (3)
Device.identifier.type.coding.code C F C F (3) C F (3)
Device.identifier.type.coding.system C F C F (3) C F (3)
Device.identifier.extension D
Device.displayName
Device.definition C C D C
Device.udiCarrier C C C D C C C C I C C D
Device.udiCarrier.extension
Device.udiCarrier.modifierExtension
Device.udiCarrier.deviceIdentifier C C D C C C
Device.udiCarrier.issuer C
Device.udiCarrier.jurisdiction
Device.udiCarrier.carrierAIDC C
Device.udiCarrier.carrierHRF C
Device.udiCarrier.entryType C
Device.status C D C I C B M
Device.availabilityStatus
Device.biologicalSourceEvent
Device.manufacturer C C C D C D D C
Device.manufactureDate C C C
Device.expirationDate C C C C C C
Device.lotNumber C C C C C C
Device.serialNumber C C C D
Device.name
Device.name.extension
Device.name.modifierExtension
Device.name.value
Device.name.type
Device.name.display
Device.modelNumber C C C C D
Device.partNumber C C D
Device.category
Device.type C B M C B M B M B M B M D C B M C B M C B M C B M B M C B M B M C B M C B M C D B M B M B M B M D B M D B M B M B M B M C B M C B M C B M C C B M C D B M C B M C B M
Device.type.text D D D
Device.type.coding S C D (2) S C D (2)
Device.type.coding.code C C F D C F D
Device.type.coding.version
Device.type.coding.system C C F D C F D
Device.version C C C C C C D C D C C
Device.version.extension
Device.version.modifierExtension
Device.version.type C C C C C
Device.version.type.text F
Device.version.type.coding S C (2) S C (2) D B M
Device.version.type.coding.code C D C D
Device.version.type.coding.version
Device.version.type.coding.system C F C F
Device.version.component C C C
Device.version.installDate
Device.version.value C C
Device.conformsTo
Device.conformsTo.extension
Device.conformsTo.modifierExtension
Device.conformsTo.category
Device.conformsTo.specification
Device.conformsTo.version
Device.property C C D C S D (4) S C D (4)
Device.property.valueCode C (3) C (3)
Device.property.valueCode.coding S C (3) S C (3)
Device.property.valueCode.coding.code C D (2) C D (2)
Device.property.valueCode.coding.version
Device.property.valueCode.coding.system C F D (2) C F D (2)
Device.property.valueQuantity C D (3) C D (3)
Device.property.valueQuantity.code C F D C F D
Device.property.valueQuantity.system C F D C F D
Device.property.valueQuantity.value C D C D
Device.property.extension
Device.property.modifierExtension
Device.property.type D B M (3) D B M (3)
Device.property.type.text D (3) D (3)
Device.property.type.coding S C (4) C (3)
Device.property.type.coding.code C D (3) C D (3)
Device.property.type.coding.version
Device.property.type.coding.system C F (3) C F (3)
Device.property.value[x]
Device.mode
Device.cycle
Device.duration
Device.owner C I C D C
Device.contact C C
Device.location C C D C C C
Device.url C C C
Device.endpoint
Device.gateway
Device.note C C
Device.note.text D
Device.note.author[x] S C D (2) C
Device.safety C C D B M C B M
Device.safety.coding
Device.safety.coding.code B M
Device.safety.coding.system D D D
Device.parent C C D C C C C
S: There is slicing defined in the element(s)
C: There is cardinality erstrictions defined in the element(s)
I: There is invariants defined in the element(s)
F: There is a fixed or pattern value defined in the element(s)
D: There is document provided in the element(s)
B: There is terminology bindings defined in the element(s)
M: At least one of the element(s) has must-support = true
(N): The number of elements if > 1

Produced 08 Sep 2023