Content

This page lists reference documents, submission files, and acknowledgment files across three tabs. The Submissions tab consists of submission files generated for the device identification object and submitted to the regulatory authority. The ACKs tab consists of acknowledgment files received from the regulatory authority.

This page discusses:

Reference Documents

For information about the fields in this tab, see Documents and Content in the Business Process Services - Common User's Guide.

Submissions

The submissions are applicable for the device identifications that are created only in USA.

Important: This app uses contact cell number and email id to regulatory authority like FDA, as is often required in highly regulated industries. You cannot delete or modify the personal data contained in the Submission. You should carefully review your use cases associated with submission to regulatory authority to ensure that the specific business requirements associated with them are being met, while still adhering to good personal data management practices.
Field Description
File Name Name of the submission file.
Format File format.
File Size File size in bytes.
Actions : Download the file.

ACKs

Field Description
File Name Name of the acknowledgment file.
Originated Date when the acknowledgment file was created.
Actions : Download the file.