# Medical Device Reporting: Electronic Submission Requirements; Correcting Amendments
> **Food and Drug Administration** · Final rule; correcting amendments. · Published 2015-02-27 · Effective 2015-08-14 · 80 FR 10586
## Document
- **Document number:** 2015-03943
- **Category:** fda-device
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 80 FR 10586
- **CFR reference:** 21 CFR 803
- **Publication date:** 2015-02-27
- **Effective date:** 2015-08-14
- **HHS docket:** Docket No. FDA-2008-N-0393
## Abstract

The Food and Drug Administration (FDA) is amending its regulation regarding postmarket electronic Medical Device Reporting (eMDR) to address the unintentional removal of certain provisions of the Unique Device Identification (UDI) System regulations and to update the contact information listed in the regulations.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/2015/02/27/2015-03943/medical-device-reporting-electronic-submission-requirements-correcting-amendments)
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