Generated Narrative: StructureDefinition EHDSDeviceLaboratoryObligations Language: en Name Flags Card. Type Description & Constraints EHDSDevice 0..* EHDSDevice Device model #xD; instanceIdentifier O 0..* Identifier Identifier of the device instance Obligations Actor SHOULD:able-to-populate Producer #xD; udi O 0..* Identifier Unique Device Identifier (UDI) value Obligations Actor SHALL:able-to-populate Producer SHALL:process Consumer #xD; manufacturer O 0..1 string Name of device manufacturer. If the manufacturer code is included in an identifier, manufacturer must correspond to that code. Obligations Actor SHOULD:able-to-populate Producer SHOULD:display Consumer #xD; lotNumber O 0..1 string Lot number of device. May be omitted if included in an identifier. Obligations Actor SHOULD:able-to-populate Producer #xD; name O 0..* Base The name and name type of the device. Obligations Actor SHOULD:able-to-populate Producer SHOULD:display Consumer #xD; value O 1..1 string The name of the device as known to e.g. the manufacturer and/or patient Obligations Actor SHALL:able-to-populate Producer SHALL:display Consumer #xD; type O 1..1 CodeableConcept The type of name, e.g. UDI Label name, user friendly name Obligations Actor SHALL:able-to-populate Producer #xD; modelNumber O 0..1 string The manufacturer's model number for the device Obligations Actor SHOULD:able-to-populate Producer #xD; version O 0..* string The actual design of the device and/or software version running on the device Obligations Actor SHOULD:able-to-populate Producer #xD; note O 0..1 string Device note and/or comment Obligations Actor SHALL:able-to-populate Producer SHALL:display Consumer #xD; Documentation for this format
Obligations for the logical model of device in the scope of laboratory use case
Consumer system SHALL consider the value to assees comparability of the result values if device is the author of the observation.
Name of device manufacturer. If the manufacturer code is included in an identifier, manufacturer must correspond to that code.
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The date and time beyond which this device is no longer valid or should not be used (if applicable)
Lot number of device. May be omitted if included in an identifier.
Serial number assigned by the manufacturer. May be omitted if included in an identifier.
The name of the device as known to e.g. the manufacturer and/or patient
The type of name, e.g. UDI Label name, user friendly name
The manufacturer's model number for the device
The actual design of the device and/or software version running on the device