This
page
is
part
of
the
FHIR
Specification
(v3.0.2:
STU
3).
(v3.3.0:
R4
Ballot
2).
The
current
version
which
supercedes
this
version
is
5.0.0
.
For
a
full
list
of
available
versions,
see
the
Directory
of
published
versions
.
Page
versions:
R5
R3
| Orders and Observations Work Group | Maturity Level : N/A | Ballot Status : Informative | Compartments : Device |
This is the narrative for the resource. See also the XML or JSON format. This example conforms to the profile Device .
Generated Narrative with Details
id : example-udi2
| - | DeviceIdentifier | Name | Jurisdiction | Issuer |
| * | A9999XYZ100T0474 | Bone,Putty Demineralized | http://hl7.org/fhir/NamingSystem/fda-udi | http://hl7.org/fhir/NamingSystem/iccbba-other |
status : inactive
manufacturer : Acme Devices, Inc
manufactureDate : 01/02/2013
expirationDate : 01/02/2014
patient : Patient/example
Usage note: every effort has been made to ensure that the examples are correct and useful, but they are not a normative part of the specification.