federal_register: 2014-13568
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| document_number | title | type | abstract | publication_date | pub_year | pub_month | html_url | pdf_url | agency_names | agency_ids | excerpts | regulation_id_numbers |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 2014-13568 | Global Unique Device Identification Database; Guidance for Industry; Availability | Notice | The Food and Drug Administration (FDA) is announcing the availability of the guidance entitled "Global Unique Device Identification Database (GUDID): Guidance for Industry". FDA has updated sections of the document, "Global Unique Device Identification (GUDID): Draft Guidance for Industry" in order to finalize the sections with the most questions from GUDID submitters. The guidance includes information about how device labelers (in most instances, the device manufacturer) will interface with the GUDID by establishing GUDID accounts and beginning their initial submissions. Draft guidance sections on the device identifier (DI) module have not been finalized in this document and will be addressed in a future document. | 2014-06-11 | 2014 | 6 | https://www.federalregister.gov/documents/2014/06/11/2014-13568/global-unique-device-identification-database-guidance-for-industry-availability | https://www.govinfo.gov/content/pkg/FR-2014-06-11/pdf/2014-13568.pdf | Health and Human Services Department; Food and Drug Administration | 221,199 | The Food and Drug Administration (FDA) is announcing the availability of the guidance entitled "Global Unique Device Identification Database (GUDID): Guidance for Industry". FDA has updated sections of the document, "Global Unique Device Identification... |