This resource identifies an instance or a type of a manufactured item that is used in the provision of healthcare without being substantially changed through that activity. The device may be a medical or non-medical device. Medical devices include durable (reusable) medical equipment, implantable devices, as well as disposable equipment used for diagnostic, treatment, and research for healthcare and public health. Non-medical devices may include items such as a machine, cellphone, computer, application, etc.

Allows institutions to track their devices.

Unique instance identifiers assigned to a device by manufacturers other organizations or owners.

The barcode string from a barcode present on a device label or package may identify the instance, include names given to the device in local usage, or may identify the type of device. If the identifier identifies the type of device, Device.type element should be used. For UDI , this element corresponds to the variable portion of the UDI that identifies the serial number of a specific device. See UDI mappings for a complete mapping of UDI parts to Device.

Unique device identifier (UDI) assigned to device label or package.

UDI may identify an unique instance of a device, or it may only identify the type of the device. See UDI mappings for a complete mapping of UDI parts to Device.

The device identifier (DI) is a mandatory, fixed portion of a UDI that identifies the labeler and the specific version or model of a device.

Name of device as used in labeling or catalog.

Use the Device.type for a generic type or kind of device name. Note the GUDID lists the name as the 'Brand Name'.

The identity of the authoritative source for UDI generation within a jurisdiction. All UDIs are globally unique within a single namespace. namespace with the appropriate repository uri as the system. For example, UDIs of devices managed in the U.S. by the FDA, the value is http://hl7.org/fhir/NamingSystem/fda-udi.

Allows a recipient of a UDI to know which database will contain the UDI-associated metadata.

The full UDI carrier as the human readable form (HRF) representation of the barcode string as printed on the packaging of the device.

If separate barcodes for DI and PI are present, concatenate the string with DI first and in order of human readable expression on label.

The full UDI carrier of the Automatic Identification and Data Capture (AIDC) technology representation of the barcode string as printed on the packaging of the device - E.g e.g., a barcode or RFID. Because of limitations on character sets in XML and the need to round-trip JSON data through XML, AIDC Formats SHALL be base64 encoded.

The AIDC form of UDIs should be scanned or otherwise used for the identification of the device whenever possible to minimize errors in records resulting from manual transcriptions. If separate barcodes for DI and PI are present, concatenate the string with DI first and in order of human readable expression on label.

Organization that is charged with issuing UDIs for devices. For example, the US FDA issuers include : 1)

1. GS1: http://hl7.org/fhir/NamingSystem/gs1-di, 2)
2. HIBCC: http://hl7.org/fhir/NamingSystem/hibcc-dI, 3)
3. ICCBBA for blood containers: http://hl7.org/fhir/NamingSystem/iccbba-blood-di, 4)
4. ICCBA for other devices: http://hl7.org/fhir/NamingSystem/iccbba-other-di.

A coded entry to indicate how the data was entered.

Supports a way to distinguish hand entered from machine read data.

Status of the Device availability.

This element is labeled as a modifier because the status contains the codes inactive and entered-in-error that mark the device (record)as not currently valid.

Code or identifier to identify a kind of device.

Lot number assigned by the manufacturer.

A name of the manufacturer.

The date and time when the device was manufactured.

The date and time beyond which this device is no longer valid or should not be used (if applicable).

The "model" "model" is an identifier assigned by the manufacturer to identify the product by its type. This number is shared by the all devices sold as the same type.

The version of the device, if the device has multiple releases under the same model, or if the device is software or carries firmware.

Patient information, If the device is affixed to a person.

If the device is implanted in a patient, then need to associate the device to the patient.

An organization that is responsible for the provision and ongoing maintenance of the device.

Contact details for an organization or a particular human that is responsible for the device.

used for troubleshooting etc.

The place where the device can be found.

Device.location can be used to track device location.

A network address on which the device may be contacted directly.

If the device is running a FHIR server, the network address should be the Base URL from which a conformance statement may be retrieved.

Descriptive information, usage information or implantation information that is not captured in an existing element.

Provides additional safety characteristics about a medical device. For example devices containing latex.