Template 2.16.840.1.113883.10.20.22.4.37 Product Instance

2012‑01‑12

Template 2.16.840.1.113883.10.20.22.4.37 - ProductInstance
Id 2.16.840.1.113883.10.20.22.4.37
Classification cdaentrylevel
Context Parent nodes of template element with id 2.16.840.1.113883.10.20.22.4.37
Label conf‑669
Version valid from 2012‑01‑12 status draft
Description This clinical statement represents a particular device that was placed in or used as part of a procedure or other act. This provides a record of the identifier and other details about the given product that was used. For example, it is important to have a record that indicates not just that a hip prostheses was placed in a patient but that it was a particular hip prostheses number with a unique identifier.

The FDA Amendments Act specifies the creation of a Unique Device Identification (UDI) System that requires the label of devices to bear a unique identifier that will standardize device identification and identify the device through distribution and use.

The UDI should be sent in the participantRole/id.
Used in 1 template:

Id Name as of
2.16.840.1.113883.10.20.22.4.50 Non-MedicinalSupplyActivity  Non-Medicinal Supply Activity 2012‑01‑12
link11 Dependency: 2.16.840.1.113883.10.20.22.2.23 MedicalEquipmentSection  Medical Equipment Section 2012‑01‑12
Item DT Card Conf Desc Label
cda:participantRole
conf-669
treetree @classCode
1..1 F MANU
treetree cda:templateId
II 1..1 M conf‑7901
treeblank treetree @root
1..1 F 2.16.840.1.113883.10.20.22.4.37
treetree cda:id
II 1..* M conf‑7902
treetree cda:playingDevice
1..1 M conf‑7903
treeblank treetree cda:code
CE 0..1 R conf‑7904
treetree cda:scopingEntity
1..1 M conf‑7905
treeblank treetree cda:id
II 1..* M conf‑7908