UDI Information Page
The UDI information page provides tools for managing the details and collection of information associated with UDIs. The page has menu actions and tabs for managing information about the UDIs. On the Actions menu, you can perform various actions on UDIs.
Tabs
The following tabs are available on both FDA UDI and UDI Super Set information page:
Tab
Description
Details
The FDA UDI submission Details tab contains following sections:
The General section displays the general FDA UDI submission information.
The Transmission Details section displays the number of attempts of FDA UDI submission and other related details. For more information, see Viewing Information for FDA UDI Submissions.
The UDI Super Set Details tab contains General section which displays the general UDI Super Set information.
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The UDI Super Set Details tab does not contain Transmission Details section.
Related Information
Displays the related product and related template to UDI.
History
Displays the version history of UDI.
Routing/Process History
Displays the UDI process status and task history.
Members
Displays information about the UDI roles. The Members table provides action to add and manage members for UDIs. Assign the UDI Approver, UDI Creator, or Library Manager roles, depending on the role the user should be assigned to. For more information, see Members Table.
Actions
The UDI information page contains a list of menu actions available from the upper left area of the page. The availability of these actions depends on the workflow status of the UDIs, as well as your access to it.
Actions
Description
Rename
Allows you to modify the name and other attributes of UDI.
Set State
Allows you to set the UDI lifecycle state to Approval, Closed and Canceled. For more information, see Setting the State of an Object.
Create Follow Up
Allows you to create a new iteration of the UDI. After creating a follow-up task, the new iteration of the UDI undergoes through the same lifecycle to be submitted to the regulatory agency.
Link to Part
Allows you to link UDIs to a part. The UDIs can only be linked to one part.
If the UDI is already linked to a part, this action is not visible.
Edit Access Control
Allows you to set the access permissions. Use the Access Table (Single Object) to manage the access permissions in the UDI.
Edit Security Labels
Allows you to view and change the security label values. If you have required permissions, you can change the security label values that are in place for the UDI.
Undo Reservation
When this action is enabled, it indicates that another user has the UDI reserved for modification. You can use this action to manually revoke their reservation and allow another user to modify the object.
A confirmation message appears with details about the user and the action they are performing.
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This action is only available to site and organization administrators.
Compare UDI Super Set
Allows you to compare the UDI Super Set with the previous follow up, in case of non-revisable Super Set, and. in case of revisable Super Set, allows you to compare the UDI Super Set with the previous revision.
See Actions Common Among Objects for a list of common actions available in Windchill.
On the FDA UDI Details page, the Transmission Details table contains the following information:
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The following section does not apply to UDI Super Set.
Column
Description
Attempt
Number of submission attempts.
Transmission Status
The status of the UDI submission (for example, successful, delayed, failed, or submitting).
View HL7
Click the XML icon to view the HL7 report in XML format.
Acknowledgement 1 Receipt Date
The date the system received the first acknowledgement from the FDA.
Acknowledgement 2 Receipt Date
The date the system received the second acknowledgement from the FDA.
Acknowledgement 3 Receipt Date
The date the system received the third acknowledgement from the FDA.
Delayed Comment
If the submission was delayed, information from the Delayed Comment field appears here.
Communication ID
A value assigned by the communication delegate when the submission was sent to the FDA. This is a unique identifier within the AS2 server.
Message ID
A value assigned by the AS2 server to uniquely identify the submission to the FDA. This value is included in Acknowledgement 1.
Core ID
A value assigned by the FDA to uniquely identify the submission. This value is included in Acknowledgement 2.
To view additional details, click the acknowledgement details icon . Under UDI Transmission Acknowledgements, you can view the following information:
Column
Description
Number
Number of submissions.
Transmission Status
The status of the communication with the FDA. It can be submitting, successful, or failed.
Message Summary
A summary of the error message returned by the FDA, if applicable.
Date Received
The date the system received the acknowledgement from the FDA.
FDA Message Report
System messages from the FDA.
Under Acknowledgement 3 Errors, if the transmission failed or was delayed, you can view error messages to see why the transmission failed or was delayed. If the transmission was successful, no error messages appear.
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You can also view the UDI status in the State column of the Folder Contents or My Tasks table.
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