Resource StructureDefinition/FHIR Server from package nictiz.fhir.nl.stu3.zib2017#2.2.20 (141 ms)
| Package | nictiz.fhir.nl.stu3.zib2017 |
| Type | StructureDefinition |
| Id | Id |
| FHIR Version | R3 |
| Source | https://simplifier.net/resolve?scope=nictiz.fhir.nl.stu3.zib2017@2.2.20&canonical=http://nictiz.nl/fhir/StructureDefinition/zib-MedicalDeviceProduct |
| Url | http://nictiz.nl/fhir/StructureDefinition/zib-MedicalDeviceProduct |
| Version | 2.0.6 |
| Status | active |
| Name | Zib MedicalDevice Product |
| Title | HCIM MedicalDevice Product |
| Experimental | False |
| Realm | nl |
| Authority | hl7 |
| Description | This 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. |
| Purpose | Data on medical aids is recorded for several reasons. Knowledge of the presence of these implants enables tracing and taking the aid or device into account in diagnostic or therapeutic procedures, care and transport.
Examples include:
* Consequences for transportation, toilet use, etc., in the case of a wheelchair;
* A pacemaker can be of medical importance, but also has consequences for planning radiological exams. |
| Copyright | CC0 |
| Type | Device |
| Kind | resource |
Resources that use this resource
Resources that this resource uses
Source
{
"resourceType" : "StructureDefinition",
"id" : "zib-MedicalDeviceProduct",
"url" : "http://nictiz.nl/fhir/StructureDefinition/zib-MedicalDeviceProduct",
"version" : "2.0.6",
"name" : "Zib MedicalDevice Product",
"title" : "HCIM MedicalDevice Product",
"status" : "active",
"publisher" : "Nictiz",
"contact" : [
{
"name" : "Nictiz",
"telecom" : [
{
"system" : "url",
"value" : "https://www.nictiz.nl",
"use" : "work"
}
]
}
],
"description" : "This resource is part of MedicalDevice as defined by the Dutch Health and Care Information models (Dutch: Zorginformatiebouwsteen or ZIB) version 3.1, release 2017.\r\n\r\nMedical 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.",
"purpose" : "Data on medical aids is recorded for several reasons. Knowledge of the presence of these implants enables tracing and taking the aid or device into account in diagnostic or therapeutic procedures, care and transport.\r\n\r\nExamples include: \r\n* Consequences for transportation, toilet use, etc., in the case of a wheelchair;\r\n* A pacemaker can be of medical importance, but also has consequences for planning radiological exams.",
"copyright" : "CC0",
"fhirVersion" : "3.0.2",
"mapping" : [
{
"identity" : "hcim-medicaldevice-v3.1-2017EN",
"uri" : "https://zibs.nl/wiki/MedicalDevice-v3.1(2017EN)",
"name" : "HCIM MedicalDevice-v3.1(2017EN)"
},
{
"identity" : "hcim-laboratorytestresult-v4.1-2017EN",
"uri" : "https://zibs.nl/wiki/LaboratoryTestResult-v4.1(2017EN)",
"name" : "HCIM LaboratoryTestResult-v4.1(2017EN)"
},
{
"identity" : "hcim-basicelements-v1.0-2017EN",
"uri" : "https://zibs.nl/wiki/BasicElements-v1.0(2017EN)",
"name" : "HCIM BasicElements-v1.0(2017EN)"
},
{
"identity" : "hcim-medicaldevice-v3.0-2016EN",
"uri" : "https://zibs.nl/wiki/MedicalDevice-v3.0(2016EN)",
"name" : "HCIM MedicalDevice-v3.0(2016EN)"
},
{
"identity" : "hcim-medicaldevice-v1.2-2015EN",
"uri" : "https://zibs.nl/wiki/MedicalDevice-v1.2(2015EN)",
"name" : "HCIM MedicalDevice-v1.2(2015EN)"
}
],
"kind" : "resource",
"abstract" : false,
"type" : "Device",
"baseDefinition" : "http://hl7.org/fhir/StructureDefinition/Device",
"derivation" : "constraint",
"differential" : {
"element" : [
{
"id" : "Device",
"path" : "Device",
"short" : "Product",
"definition" : "The medical aid used (internally or externally).",
"alias" : [
"Product"
],
"mapping" : [
{
"identity" : "hcim-medicaldevice-v1.2-2015EN",
"map" : "NL-CM:10.1.2",
"comment" : "Product"
},
{
"identity" : "hcim-medicaldevice-v3.0-2016EN",
"map" : "NL-CM:10.1.2",
"comment" : "Product"
},
{
"identity" : "hcim-medicaldevice-v3.1-2017EN",
"map" : "NL-CM:10.1.2",
"comment" : "Product"
}
]
},
{
"id" : "Device.identifier",
"path" : "Device.identifier",
"slicing" : {
"discriminator" : [
{
"type" : "pattern",
"path" : "type"
}
],
"rules" : "open"
},
"short" : "ProductID",
"definition" : "Unique identification of the product, such as the serial number. \r\nFrequently used coding systems are HIBC and GTIN.\r\nIf the law requires this to be registered on the basis of a UDI (Unique Device Identifier), the unique identification must consist of a UDI-DI (Device Identifier) and a UDI-PI (Production Identifier(s)). See http://www.gs1.org/healthcare/udi for more information. \r\n\r\nThe UDI-DI must be recorded in reference to GS1 GTIN (01) encryptions, with which for example a firm is linked to the product type. The UDI-PI must consist of the following: application identifier (AI); expiration date (17) and serial number (21) and/or batch or lot number (10).",
"alias" : [
"ProductID"
],
"mapping" : [
{
"identity" : "hcim-medicaldevice-v1.2-2015EN",
"map" : "NL-CM:10.1.4",
"comment" : "ProductID"
},
{
"identity" : "hcim-medicaldevice-v3.0-2016EN",
"map" : "NL-CM:10.1.4",
"comment" : "ProductID"
},
{
"identity" : "hcim-medicaldevice-v3.1-2017EN",
"map" : "NL-CM:10.1.4",
"comment" : "ProductID"
},
{
"identity" : "hcim-basicelements-v1.0-2017EN",
"map" : "NL-CM:0.0.6",
"comment" : "IdentificationNumber"
}
]
},
{
"id" : "Device.identifier:serialNumber",
"path" : "Device.identifier",
"sliceName" : "serialNumber",
"short" : "serial number (21) part of the UDI",
"max" : "1",
"mapping" : [
{
"identity" : "hcim-medicaldevice-v3.1-2017EN",
"map" : "NL-CM:10.1.4",
"comment" : "ProductID. serial number (21) part of the UDI"
}
]
},
{
"id" : "Device.identifier:serialNumber.type",
"path" : "Device.identifier.type",
"min" : 1,
"patternCodeableConcept" : {
"coding" : [
{
"system" : "http://hl7.org/fhir/identifier-type",
"code" : "SNO"
}
]
}
},
{
"id" : "Device.identifier:serialNumber.type.coding",
"path" : "Device.identifier.type.coding",
"min" : 1,
"max" : "1"
},
{
"id" : "Device.identifier:serialNumber.type.coding.system",
"path" : "Device.identifier.type.coding.system",
"min" : 1,
"fixedUri" : "http://hl7.org/fhir/identifier-type"
},
{
"id" : "Device.identifier:serialNumber.type.coding.code",
"path" : "Device.identifier.type.coding.code",
"min" : 1,
"fixedCode" : "SNO"
},
{
"id" : "Device.identifier:serialNumber.value",
"path" : "Device.identifier.value",
"min" : 1
},
{
"id" : "Device.udi.deviceIdentifier",
"path" : "Device.udi.deviceIdentifier",
"short" : "application identifier (AI) (01) part of the udi",
"mapping" : [
{
"identity" : "hcim-medicaldevice-v3.1-2017EN",
"map" : "NL-CM:10.1.4",
"comment" : "ProductID. application identifier (AI) (01) part of the udi"
}
]
},
{
"id" : "Device.udi.carrierHRF",
"path" : "Device.udi.carrierHRF",
"short" : "ProductID",
"definition" : "Unique identification of the product, such as the serial number.\r\n\r\nFrequently used coding systems are HIBC and GTIN. If the law requires this to be registered on the basis of a UDI (Unique Device Identifier), the unique identification must consist of a UDI-DI (Device Identifier) and a UDI-PI (Production Identifier(s)). See http://www.gs1.org/healthcare/udi for more information.\r\n\r\nThe UDI-DI must be recorded in reference to GS1 GTIN (01) encryptions, with which for example a firm is linked to the product type. The UDI-PI must consist of the following: application identifier (AI); expiration date (17) and serial number (21) and/or batch or lot number (10).",
"mapping" : [
{
"identity" : "hcim-medicaldevice-v3.1-2017EN",
"map" : "NL-CM:10.1.4",
"comment" : "ProductID"
}
]
},
{
"id" : "Device.type",
"path" : "Device.type",
"short" : "ProductType",
"definition" : "The code of the type of product.",
"alias" : [
"ProductType"
],
"binding" : {
"strength" : "extensible",
"description" : "The code of the type of product.",
"valueSetReference" : {
"reference" : "http://decor.nictiz.nl/fhir/ValueSet/2.16.840.1.113883.2.4.3.11.60.40.2.10.1.1--20171231000000",
"display" : "ProductTypeCodelijst"
}
},
"mapping" : [
{
"identity" : "hcim-medicaldevice-v1.2-2015EN",
"map" : "NL-CM:10.1.3",
"comment" : "ProductType"
},
{
"identity" : "hcim-medicaldevice-v3.0-2016EN",
"map" : "NL-CM:10.1.3",
"comment" : "ProductType"
},
{
"identity" : "hcim-medicaldevice-v3.1-2017EN",
"map" : "NL-CM:10.1.3",
"comment" : "ProductType"
}
]
},
{
"id" : "Device.type.coding.system",
"path" : "Device.type.coding.system",
"min" : 1
},
{
"id" : "Device.type.coding.code",
"path" : "Device.type.coding.code",
"min" : 1
},
{
"id" : "Device.type.text",
"extension" : [
{
"url" : "http://hl7.org/fhir/StructureDefinition/elementdefinition-translatable",
"valueBoolean" : true
}
],
"path" : "Device.type.text",
"comment" : "For LaboratoryTestResult.Specimen.SpecimenSource a device may be recorded as a subject of the Specimen. For example if the material is not collected directly from the patient but comes from a patient-related object, e.g. a catheter tip. This source of material can be recorded here.",
"mapping" : [
{
"identity" : "hcim-laboratorytestresult-v4.1-2017EN",
"map" : "NL-CM:13.1.29",
"comment" : "SpecimenSource"
}
]
},
{
"id" : "Device.lotNumber",
"path" : "Device.lotNumber",
"short" : "batch or lot number (10) part of the UDI",
"mapping" : [
{
"identity" : "hcim-medicaldevice-v3.1-2017EN",
"map" : "NL-CM:10.1.4",
"comment" : "ProductID. batch or lot number (10) part of the UDI"
}
]
},
{
"id" : "Device.expirationDate",
"path" : "Device.expirationDate",
"short" : "expiration date (17) part of the UDI",
"mapping" : [
{
"identity" : "hcim-medicaldevice-v3.1-2017EN",
"map" : "NL-CM:10.1.4",
"comment" : "ProductID. expiration date (17) part of the UDI"
}
]
},
{
"id" : "Device.patient",
"path" : "Device.patient",
"type" : [
{
"code" : "Reference",
"targetProfile" : "http://fhir.nl/fhir/StructureDefinition/nl-core-patient"
}
],
"mapping" : [
{
"identity" : "hcim-basicelements-v1.0-2017EN",
"map" : "NL-CM:0.0.11",
"comment" : "Subject"
}
]
},
{
"id" : "Device.owner",
"path" : "Device.owner",
"type" : [
{
"code" : "Reference",
"targetProfile" : "http://fhir.nl/fhir/StructureDefinition/nl-core-organization"
}
]
},
{
"id" : "Device.location",
"path" : "Device.location",
"type" : [
{
"code" : "Reference",
"targetProfile" : "http://fhir.nl/fhir/StructureDefinition/nl-core-location"
}
]
},
{
"id" : "Device.note.text",
"path" : "Device.note.text",
"short" : "ProductDescription",
"definition" : "Textual description of the product.",
"alias" : [
"ProductOmschrijving"
],
"mapping" : [
{
"identity" : "hcim-medicaldevice-v1.2-2015EN",
"map" : "NL-CM:10.1.13",
"comment" : "ProductDescription"
},
{
"identity" : "hcim-medicaldevice-v3.0-2016EN",
"map" : "NL-CM:10.1.13",
"comment" : "ProductDescription"
},
{
"identity" : "hcim-medicaldevice-v3.1-2017EN",
"map" : "NL-CM:10.1.13",
"comment" : "ProductDescription"
}
]
}
]
},
"text" : {
}
}
XIG built as of ??metadata-date??. Found ??metadata-resources?? resources in ??metadata-packages?? packages.
FHIR