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Device use model - EHDS Logical Information Models v0.1.0


IDPathMinMaxType(s)ShortDefinitionBinding StrengthBinding DescriptionLäkemedelsverketRegion VästerbottenIneraE-hälso-myndigheten
EHDSDeviceUseEHDSDeviceUse0*
Device use modelC.25 - EHDS refined base model for Device Use





EHDSDeviceUse.identifierEHDSDeviceUse.identifier0*IdentifierC.25.1 - IdentifierAn identifier for this statement.





EHDSDeviceUse.statusEHDSDeviceUse.status01CodeableConceptC.25.2 - StatusCurrent status of the Device Usage.preferredHL7 device-statement-status



EHDSDeviceUse.implantDateEHDSDeviceUse.implantDate01dateTimeC.25.3 - Implant dateDate when procedure was performed.





EHDSDeviceUse.endDateEHDSDeviceUse.endDate01dateTimeC.25.4 - End dateDate when the device was explanted from the patient or the external device was no longer in use; likewise when the device is planned to be explanted.





EHDSDeviceUse.deviceEHDSDeviceUse.device11

Reference

(https://www.xt-ehr.eu/specifications/fhir/StructureDefinition/EHDSDevice)

C.25.5 - DeviceThe details of the device used.





EHDSDeviceUse.subjectEHDSDeviceUse.subject11

Reference

(https://www.xt-ehr.eu/specifications/fhir/StructureDefinition/EHDSPatient)

C.25.6 - SubjectThe patient using the device.





EHDSDeviceUse.bodySiteEHDSDeviceUse.bodySite01CodeableConceptC.25.7 - Body siteAnatomical location of the device. May include laterality.





EHDSDeviceUse.noteEHDSDeviceUse.note0*NarrativeC.25.8 - NoteDetails about the device statement that were not represented at all or sufficiently in one of the attributes provided in a class. These may include for example a comment, an instruction, or a note associated with the statement.





EHDSDeviceUse.recordedEHDSDeviceUse.recorded01dateTimeC.25.9 - RecordedDate and time at which the statement was made/recorded.





EHDSDeviceUse.sourceEHDSDeviceUse.source01Reference(https://www.xt-ehr.eu/specifications/fhir/StructureDefinition/EHDSPatient|https://www.xt-ehr.eu/specifications/fhir/StructureDefinition/EHDSHealthProfessional|https://www.xt-ehr.eu/specifications/fhir/StructureDefinition/EHDSRelatedPerson)C.25.10 - SourceWho reported the device was being used by the patient.







Exporterat från logisk modell "Device model" (under arbete)

Device model - EHDS Logical Information Models v0.1.0


IDPathMinMaxType(s)ShortDefinitionBinding StrengthBinding DescriptionLäkemedelsverketRegion VästerbottenIneraE-hälso-myndigheten
EHDSDeviceEHDSDevice0*
Device modelC.12 - EHDS refined base model for Device information





EHDSDevice.identifierEHDSDevice.identifier1*IdentifierC.12.1 - IdentifierAn identifier of the device which is unique within in a defined scope. Multiple identifiers can be used.





EHDSDevice.manufacturerEHDSDevice.manufacturer01stringC.12.2 - ManufacturerName of device manufacturer





EHDSDevice.manufactureDateEHDSDevice.manufactureDate01dateTimeC.12.3 - Manufacture dateThe date and time when the device was manufactured





EHDSDevice.expiryDateEHDSDevice.expiryDate01dateTimeC.12.4 - Expiry dateThe date and time beyond which this device is no longer valid or should not be used (if applicable).





EHDSDevice.lotNumberEHDSDevice.lotNumber01stringC.12.5 - Lot numberLot number of manufacture





EHDSDevice.serialNumberEHDSDevice.serialNumber01stringC.12.6 - Serial numberSerial number assigned by the manufacturer





EHDSDevice.nameEHDSDevice.name0*stringC.12.7 - NameThe name and name type of the device as known to the manufacturer and/or patient





EHDSDevice.modelNumberEHDSDevice.modelNumber01stringC.12.8 - Model numberThe manufacturer's model number for the device





EHDSDevice.versionEHDSDevice.version01stringC.12.9 - VersionThe actual design of the device or software version running on the device





EHDSDevice.typeEHDSDevice.type0*CodeableConceptC.12.10 - TypeDevice typepreferredSNOMED CT, EMDN



EHDSDevice.noteEHDSDevice.note0*NarrativeC.12.11 - NoteDevice notes and comments