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. 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. If the element is present, it must have either a @value, an @id, or extensions Unique instance identifiers assigned to a device by manufacturers other organizations or owners. [Unique device identifier (UDI)](device.html#5.11.3.2.2) assigned to device label or package. Status of the Device availability. 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 The date and time beyond which this device is no longer valid or should not be used (if applicable).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" 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. 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. The place where the device can be found. A network address on which the device may be contacted directly. 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. 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. 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. The identity of the authoritative source for UDI generation within a jurisdiction. All UDIs are globally unique within a single 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. The full UDI carrier as the human readable form (HRF) representation of the barcode string as printed on the packaging of the device. 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 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. Organization that is charged with issuing UDIs for devices. For example, the US FDA issuers include : 1) GS1: http://hl7.org/fhir/NamingSystem/gs1-di, 2) HIBCC: http://hl7.org/fhir/NamingSystem/hibcc-dI, 3) ICCBBA for blood containers: http://hl7.org/fhir/NamingSystem/iccbba-blood-di, 4) ICCBA for other devices: http://hl7.org/fhir/NamingSystem/iccbba-other-di. A coded entry to indicate how the data was entered. Active Inactive Entered in Error Unknown The availability status of the device. If the element is present, it must have either a @value, an @id, or extensions BarCode RFID Manual Card Self Reported Unknown Codes to identify how UDI data was entered If the element is present, it must have either a @value, an @id, or extensions