{"database": "openregs", "table": "federal_register", "rows": [["2013-23058", "Global Unique Device Identification Database; Draft Guidance for Industry; Availability", "Notice", "The Food and Drug Administration (FDA) is announcing the availability of the draft guidance entitled \"Global Unique Device Identification Database (GUDID).\" FDA is issuing this draft guidance to communicate our current thinking of how the GUDID will operate. The guidance includes both information about how device labelers (in most instances, the device manufacturer) will interface with the GUDID, as well as information on the database elements that must be submitted to the GUDID and their definitions. We intend to publish a final guidance after the close of the comment period and our implementation of the GUDID.", "2013-09-24", 2013, 9, "https://www.federalregister.gov/documents/2013/09/24/2013-23058/global-unique-device-identification-database-draft-guidance-for-industry-availability", "https://www.govinfo.gov/content/pkg/FR-2013-09-24/pdf/2013-23058.pdf", "Health and Human Services Department; Food and Drug Administration", "221,199", "The Food and Drug Administration (FDA) is announcing the availability of the draft guidance entitled \"Global Unique Device Identification Database (GUDID).\" FDA is issuing this draft guidance to communicate our current thinking of how the GUDID will...", null]], "columns": ["document_number", "title", "type", "abstract", "publication_date", "pub_year", "pub_month", "html_url", "pdf_url", "agency_names", "agency_ids", "excerpts", "regulation_id_numbers"], "primary_keys": ["document_number"], "primary_key_values": ["2013-23058"], "units": {}, "query_ms": 30.218268046155572, "source": "Federal Register API & Regulations.gov API", "source_url": "https://www.federalregister.gov/developers/api/v1", "license": "Public Domain (U.S. Government data)", "license_url": "https://www.regulations.gov/faq"}