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FHIR IG Statistics: StructureDefinition/MedicalDevice

Packagehl7.fhir.eu.eps
TypeStructureDefinition
IdMedicalDevice
FHIR VersionR4
Sourcehttp://hl7.eu/fhir/eps/https://build.fhir.org/ig/hl7-eu/eps/StructureDefinition-MedicalDevice.html
URLhttp://hl7.eu/fhir/eps/StructureDefinition/MedicalDevice
Version0.0.1-ci
Statusdraft
Date2025-06-20T15:31:33+00:00
NameMedicalDevicePsEhn
TitleA.2.3.2 - Medical devices and implants
Realmeu
Authorityhl7
DescriptionMedical devices and implants Section A.2.3.2 of the eHN guideline.
CopyrightUsed by permission of HL7 Europe, all rights reserved Creative Commons License
Typehttp://hl7.eu/fhir/eps/StructureDefinition/MedicalDevice
Kindlogical

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Narrative

Note: links and images are rebased to the (stated) source

Generated Narrative: StructureDefinition MedicalDevice

NameFlagsCard.TypeDescription & Constraintsdoco
.. MedicalDevice 0..*BaseA.2.3.2 - Medical devices and implants
... description 0..*CodeableConceptA.2.3.2.1 Device and implant description
... identifier 0..*IdentifierA.2.3.2.2 Device ID
... implantDate 0..*dateTimeA.2.3.2.3 Implant date
... endDate 0..1dateTimeA.2.3.2.4 End date

doco Documentation for this format

Source

{
  "resourceType": "StructureDefinition",
  "id": "MedicalDevice",
  "text": {
    "status": "extensions",
    "div": "<!-- snip (see above) -->"
  },
  "url": "http://hl7.eu/fhir/eps/StructureDefinition/MedicalDevice",
  "version": "0.0.1-ci",
  "name": "MedicalDevicePsEhn",
  "title": "A.2.3.2 - Medical devices and implants",
  "status": "draft",
  "date": "2025-06-20T15:31:33+00:00",
  "publisher": "HL7 Europe",
  "contact": [
    {
      "name": "HL7 Europe",
      "telecom": [
        {
          "system": "url",
          "value": "http://hl7.eu"
        }
      ]
    }
  ],
  "description": "Medical devices and implants\nSection A.2.3.2 of the eHN guideline.",
  "jurisdiction": [
    {
      "coding": [
        {
          "system": "http://unstats.un.org/unsd/methods/m49/m49.htm",
          "code": "150",
          "display": "Europe"
        }
      ]
    }
  ],
  "copyright": "Used by permission of HL7 Europe, all rights reserved Creative Commons License",
  "fhirVersion": "4.0.1",
  "kind": "logical",
  "abstract": false,
  "type": "http://hl7.eu/fhir/eps/StructureDefinition/MedicalDevice",
  "baseDefinition": "http://hl7.org/fhir/StructureDefinition/Base",
  "derivation": "specialization",
  "snapshot": {
    "extension": [
      {
        "url": "http://hl7.org/fhir/tools/StructureDefinition/snapshot-base-version",
        "valueString": "4.0.1"
      }
    ],
    "element": [
      {
        "id": "MedicalDevice",
        "path": "MedicalDevice",
        "short": "A.2.3.2 - Medical devices and implants",
        "definition": "Medical devices and implants\nSection A.2.3.2 of the eHN guideline.",
        "min": 0,
        "max": "*",
        "base": {
          "path": "Base",
          "min": 0,
          "max": "*"
        },
        "isModifier": false
      },
      {
        "id": "MedicalDevice.description",
        "path": "MedicalDevice.description",
        "short": "A.2.3.2.1 Device and implant description",
        "definition": "Describes the patient's implanted and external medical devices and equipment upon which their health status depends. Includes devices such as cardiac pacemakers, implantable fibrillator, prosthesis, ferromagnetic bone implants, etc. of which the HP needs to be aware. - Preferred system(s): SNOMED CT GPS* EMDN",
        "min": 0,
        "max": "*",
        "base": {
          "path": "MedicalDevice.description",
          "min": 0,
          "max": "*"
        },
        "type": [
          {
            "code": "CodeableConcept"
          }
        ]
      },
      {
        "id": "MedicalDevice.identifier",
        "path": "MedicalDevice.identifier",
        "short": "A.2.3.2.2 Device ID",
        "definition": "Normalised identifier of the device instance such as UDI according to REGULATION (EU) 2017/745",
        "min": 0,
        "max": "*",
        "base": {
          "path": "MedicalDevice.identifier",
          "min": 0,
          "max": "*"
        },
        "type": [
          {
            "code": "Identifier"
          }
        ]
      },
      {
        "id": "MedicalDevice.implantDate",
        "path": "MedicalDevice.implantDate",
        "short": "A.2.3.2.3 Implant date",
        "definition": "Date when procedure was performed - Preferred system(s): ISO 8601",
        "min": 0,
        "max": "*",
        "base": {
          "path": "MedicalDevice.implantDate",
          "min": 0,
          "max": "*"
        },
        "type": [
          {
            "code": "dateTime"
          }
        ]
      },
      {
        "id": "MedicalDevice.endDate",
        "path": "MedicalDevice.endDate",
        "short": "A.2.3.2.4 End date",
        "definition": "Date 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 - Preferred system(s): ISO 8601",
        "min": 0,
        "max": "1",
        "base": {
          "path": "MedicalDevice.endDate",
          "min": 0,
          "max": "1"
        },
        "type": [
          {
            "code": "dateTime"
          }
        ]
      }
    ]
  },
  "differential": {
    "element": [
      {
        "id": "MedicalDevice",
        "path": "MedicalDevice",
        "short": "A.2.3.2 - Medical devices and implants",
        "definition": "Medical devices and implants\nSection A.2.3.2 of the eHN guideline."
      },
      {
        "id": "MedicalDevice.description",
        "path": "MedicalDevice.description",
        "short": "A.2.3.2.1 Device and implant description",
        "definition": "Describes the patient's implanted and external medical devices and equipment upon which their health status depends. Includes devices such as cardiac pacemakers, implantable fibrillator, prosthesis, ferromagnetic bone implants, etc. of which the HP needs to be aware. - Preferred system(s): SNOMED CT GPS* EMDN",
        "min": 0,
        "max": "*",
        "type": [
          {
            "code": "CodeableConcept"
          }
        ]
      },
      {
        "id": "MedicalDevice.identifier",
        "path": "MedicalDevice.identifier",
        "short": "A.2.3.2.2 Device ID",
        "definition": "Normalised identifier of the device instance such as UDI according to REGULATION (EU) 2017/745",
        "min": 0,
        "max": "*",
        "type": [
          {
            "code": "Identifier"
          }
        ]
      },
      {
        "id": "MedicalDevice.implantDate",
        "path": "MedicalDevice.implantDate",
        "short": "A.2.3.2.3 Implant date",
        "definition": "Date when procedure was performed - Preferred system(s): ISO 8601",
        "min": 0,
        "max": "*",
        "type": [
          {
            "code": "dateTime"
          }
        ]
      },
      {
        "id": "MedicalDevice.endDate",
        "path": "MedicalDevice.endDate",
        "short": "A.2.3.2.4 End date",
        "definition": "Date 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 - Preferred system(s): ISO 8601",
        "min": 0,
        "max": "1",
        "type": [
          {
            "code": "dateTime"
          }
        ]
      }
    ]
  }
}