id,agency_id,docket_id,title,document_type,subtype,posted_date,posted_year,posted_month,comment_start_date,comment_end_date,last_modified,fr_doc_num,open_for_comment,withdrawn,object_id
FDA-2017-D-6841-0017,FDA,FDA-2017-D-6841,"Unique Device Identification: Policy Regarding Compliance Dates for Class I and Unclassified Devices, Direct Marking, and Global Unique Device Identification Database Requirements for Certain Devices; Guidance for Industry and Food and Drug Administration Staff; Availability",Rule,Final Rule,2022-07-25T04:00:00Z,2022,7,2022-07-25T04:00:00Z,,2022-07-25T15:42:10Z,2022-15828,0,0,09000064851e551d
FDA-2017-D-6841-0018,FDA,FDA-2017-D-6841,"Unique Device Identification: Policy Regarding Compliance Dates for Class I and Unclassified Devices, Direct Marking, and Global Unique Device Identification Database Requirements for Certain Devices Guidance for Industry and
Food and Drug Administration Staff",Other,Guidance,2022-07-25T04:00:00Z,2022,7,2022-07-25T04:00:00Z,,2024-11-07T00:41:54Z,,1,0,09000064851e630c