Logical model for a medical device

Organization responsible for the device

Patient in whom the device is implanted or for whom it is used

The Unique Device Identifier (UDI), usually captured by scanning a barcode or RFID label, enabling unique identification of the exact device (manufacturer, type, lot number, serial number, expiration date, etc.)

Unique id for the element within a resource (for internal references). This may be any string value that does not contain spaces.

May be used to represent additional information that is not part of the basic definition of the element. To make the use of extensions safe and manageable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer can define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension.

There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.

May be used to represent additional information that is not part of the basic definition of the element and that modifies the understanding of the element in which it is contained and/or the understanding of the containing element's descendants. Usually modifier elements provide negation or qualification. To make the use of extensions safe and manageable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer can define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension. Applications processing a resource are required to check for modifier extensions.

Modifier extensions SHALL NOT change the meaning of any elements on Resource or DomainResource (including cannot change the meaning of modifierExtension itself).

There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.

Modifier extensions allow for extensions that cannot be safely ignored to be clearly distinguished from the vast majority of extensions which can be safely ignored. This promotes interoperability by eliminating the need for implementers to prohibit the presence of extensions. For further information, see the definition of modifier extensions.

The device identifier (DI) portion of the UDI

Human-readable form of the UDI

Alternative identifier when no UDI is available, e.g. a NIHDI notification number or other alternative identifier

Status of the device (active, inactive, entered-in-error, unknown)

Reason why the device has a particular status, e.g. why it is inactive or out of service

The kind of medical device, e.g. SNOMED CT code 304120007 - Cardiac pacemaker, device (physical object)

Reference to the generic definition of the device, describing general characteristics of the device type rather than the unique instance

The manufacturer that produced the device, e.g. Medtronic

The date the device was manufactured

The date after which the device may no longer be used

The lot or batch number in which the device was produced

The actual version of the device or the software version running on it

A unique identification code assigned by the manufacturer to one specific device

The name of the medical device as determined by the manufacturer

The model number of the device as assigned by the manufacturer

The actual configuration settings of a device as it operates, e.g. regulation status or time properties

Unique id for the element within a resource (for internal references). This may be any string value that does not contain spaces.

May be used to represent additional information that is not part of the basic definition of the element. To make the use of extensions safe and manageable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer can define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension.

There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.

May be used to represent additional information that is not part of the basic definition of the element and that modifies the understanding of the element in which it is contained and/or the understanding of the containing element's descendants. Usually modifier elements provide negation or qualification. To make the use of extensions safe and manageable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer can define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension. Applications processing a resource are required to check for modifier extensions.

Modifier extensions SHALL NOT change the meaning of any elements on Resource or DomainResource (including cannot change the meaning of modifierExtension itself).

There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.

Modifier extensions allow for extensions that cannot be safely ignored to be clearly distinguished from the vast majority of extensions which can be safely ignored. This promotes interoperability by eliminating the need for implementers to prohibit the presence of extensions. For further information, see the definition of modifier extensions.

Code that specifies the property

Value of the property

General notes about the device

Logical model for a medical device

Organization responsible for the device

Patient in whom the device is implanted or for whom it is used

The Unique Device Identifier (UDI), usually captured by scanning a barcode or RFID label, enabling unique identification of the exact device (manufacturer, type, lot number, serial number, expiration date, etc.)

The device identifier (DI) portion of the UDI

Human-readable form of the UDI

Alternative identifier when no UDI is available, e.g. a NIHDI notification number or other alternative identifier

Status of the device (active, inactive, entered-in-error, unknown)

Reason why the device has a particular status, e.g. why it is inactive or out of service

The kind of medical device, e.g. SNOMED CT code 304120007 - Cardiac pacemaker, device (physical object)

Reference to the generic definition of the device, describing general characteristics of the device type rather than the unique instance

The manufacturer that produced the device, e.g. Medtronic

The date the device was manufactured

The date after which the device may no longer be used

The lot or batch number in which the device was produced

The actual version of the device or the software version running on it

A unique identification code assigned by the manufacturer to one specific device

The name of the medical device as determined by the manufacturer

The model number of the device as assigned by the manufacturer

The actual configuration settings of a device as it operates, e.g. regulation status or time properties

Code that specifies the property

Value of the property

General notes about the device

Logical model for a medical device

Organization responsible for the device

Patient in whom the device is implanted or for whom it is used

The Unique Device Identifier (UDI), usually captured by scanning a barcode or RFID label, enabling unique identification of the exact device (manufacturer, type, lot number, serial number, expiration date, etc.)

Unique id for the element within a resource (for internal references). This may be any string value that does not contain spaces.

May be used to represent additional information that is not part of the basic definition of the element. To make the use of extensions safe and manageable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer can define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension.

There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.

May be used to represent additional information that is not part of the basic definition of the element and that modifies the understanding of the element in which it is contained and/or the understanding of the containing element's descendants. Usually modifier elements provide negation or qualification. To make the use of extensions safe and manageable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer can define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension. Applications processing a resource are required to check for modifier extensions.

Modifier extensions SHALL NOT change the meaning of any elements on Resource or DomainResource (including cannot change the meaning of modifierExtension itself).

There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.

Modifier extensions allow for extensions that cannot be safely ignored to be clearly distinguished from the vast majority of extensions which can be safely ignored. This promotes interoperability by eliminating the need for implementers to prohibit the presence of extensions. For further information, see the definition of modifier extensions.

The device identifier (DI) portion of the UDI

Human-readable form of the UDI

Alternative identifier when no UDI is available, e.g. a NIHDI notification number or other alternative identifier

Status of the device (active, inactive, entered-in-error, unknown)

Reason why the device has a particular status, e.g. why it is inactive or out of service

The kind of medical device, e.g. SNOMED CT code 304120007 - Cardiac pacemaker, device (physical object)

Reference to the generic definition of the device, describing general characteristics of the device type rather than the unique instance

The manufacturer that produced the device, e.g. Medtronic

The date the device was manufactured

The date after which the device may no longer be used

The lot or batch number in which the device was produced

The actual version of the device or the software version running on it

A unique identification code assigned by the manufacturer to one specific device

The name of the medical device as determined by the manufacturer

The model number of the device as assigned by the manufacturer

The actual configuration settings of a device as it operates, e.g. regulation status or time properties

Unique id for the element within a resource (for internal references). This may be any string value that does not contain spaces.

May be used to represent additional information that is not part of the basic definition of the element. To make the use of extensions safe and manageable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer can define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension.

There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.

May be used to represent additional information that is not part of the basic definition of the element and that modifies the understanding of the element in which it is contained and/or the understanding of the containing element's descendants. Usually modifier elements provide negation or qualification. To make the use of extensions safe and manageable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer can define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension. Applications processing a resource are required to check for modifier extensions.

Modifier extensions SHALL NOT change the meaning of any elements on Resource or DomainResource (including cannot change the meaning of modifierExtension itself).

There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.

Modifier extensions allow for extensions that cannot be safely ignored to be clearly distinguished from the vast majority of extensions which can be safely ignored. This promotes interoperability by eliminating the need for implementers to prohibit the presence of extensions. For further information, see the definition of modifier extensions.

Code that specifies the property

Value of the property

General notes about the device