federal_register: 2015-03943

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document_number title type abstract publication_date pub_year pub_month html_url pdf_url agency_names agency_ids excerpts
2015-03943 Medical Device Reporting: Electronic Submission Requirements; Correcting Amendments Rule 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. 2015-02-27 2015 2 https://www.federalregister.gov/documents/2015/02/27/2015-03943/medical-device-reporting-electronic-submission-requirements-correcting-amendments https://www.govinfo.gov/content/pkg/FR-2015-02-27/pdf/2015-03943.pdf Health and Human Services Department; Food and Drug Administration 221,199 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...

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