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withdrawn,object_id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
FDA-2017-D-6841-0011,FDA,FDA-2017-D-6841,Select Updates for Unique Device Identification: Policy Regarding Global Unique Device Identification Database Requirements for Certain Devices; Draft Guidance for Industry and Food and Drug Administration Staff,Other,Guidance,2021-10-14T04:00:00Z,2021,10,2021-10-14T04:00:00Z,2021-12-14T04:59:59Z,2024-11-06T23:51:53Z,,1,0,0900006484dc57d2
FDA-2017-D-6841-0010,FDA,FDA-2017-D-6841,Select Updates for Unique Device Identification: Policy Regarding Global Unique Device Identification Database Requirements for Certain Devices; Draft Guidance for Industry and Food and Drug Administration Staff; Availability,Notice,Notice of Availability,2021-10-14T04:00:00Z,2021,10,2021-10-14T04:00:00Z,,2021-10-14T16:32:28Z,2021-22308,0,0,0900006484dc53c1
FDA-2017-D-6841-0008,FDA,FDA-2017-D-6841,"Unique Device Identification: Policy Regarding Compliance Dates for Class I and Unclassified Devices and Certain Devices Requiring Direct Marking; Immediately in Effect Guidance for Industry and Food and Drug
Administration Staff; Availability",Notice,Approval,2020-07-01T04:00:00Z,2020,7,2020-07-01T04:00:00Z,,2020-07-01T19:36:57Z,2020-14082,0,0,090000648471e423
FDA-2017-D-6841-0005,FDA,FDA-2017-D-6841,Unique Device Identification: Policy Regarding Compliance Dates for Class I and Unclassified Devices and Certain Devices Requiring Direct Marking; Immediately in Effect Guidance for Industry and Food and Drug Administration Staff; Availability,Notice,Notice of Availability,2018-11-05T05:00:00Z,2018,11,2018-11-05T05:00:00Z,,2018-11-05T14:06:49Z,2018-24177,0,0,090000648389887a
FDA-2017-D-6841-0006,FDA,FDA-2017-D-6841,Unique Device Identification: Policy Regarding Compliance Dates for Class I and Unclassified Devices and Certain Devices Requiring Direct Marking Immediately in Effect Guidance for Industry and Food and Drug Administration Staff,Other,Guidance,2018-11-05T05:00:00Z,2018,11,2018-11-05T05:00:00Z,,2024-11-12T22:48:50Z,,1,0,090000648389a26b
FDA-2017-D-6841-0004,FDA,FDA-2017-D-6841,Guidance for Industry and FDA_UDI Policy for Class I and Unclassified and Direct Marking_20181105,Other,Guidance,2018-11-02T04:00:00Z,2018,11,2018-11-02T04:00:00Z,,2024-11-12T22:48:46Z,,1,0,090000648388617e
FDA-2017-D-6841-0002,FDA,FDA-2017-D-6841,Unique Device Identification: Policy Regarding Compliance Dates for Class I and Unclassified Devices Immediately in Effect Guidance for Industry and Food and Drug Administration Staff,Other,Guidance,2018-01-16T05:00:00Z,2018,1,2018-01-16T05:00:00Z,,2024-11-07T01:16:38Z,,1,0,0900006482e0d5f7
FDA-2017-D-6841-0001,FDA,FDA-2017-D-6841,"Unique Device Identification: Policy Regarding Compliance Dates for Class I and Unclassified Devices; Immediately in Effect Guidance for
Industry and Food and Drug Administration Staff; Availability",Notice,Notice of Availability,2018-01-16T05:00:00Z,2018,1,2018-01-16T05:00:00Z,,2018-01-16T16:51:42Z,2018-00550,0,0,0900006482e0b376