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10 rows where docket_id = "FDA-2017-D-6841" sorted by posted_date descending
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agency_id 1
- FDA 10
| 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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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 | None 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 | None 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 | None 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Device Identification: Policy Regarding Global Unique Device Identification Database Requirements for Certain Devices; Draft Guidance for Industry and Food and Drug Administration Staff | Other | Guidance | 2021-10-14T04:00:00Z | 2021 | 10 | 2021-10-14T04:00:00Z | 2021-12-14T04:59:59Z |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 | None 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Device Identification: Policy Regarding Global Unique Device Identification Database Requirements for Certain Devices; Draft Guidance for Industry and Food and Drug Administration Staff; Availability | Notice | Notice of Availability | 2021-10-14T04:00:00Z | 2021 | 10 | 2021-10-14T04:00:00Z |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 | None 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 | None 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 | None 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 | None 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 | None 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 | None 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 |
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CREATE TABLE documents (
id TEXT PRIMARY KEY,
agency_id TEXT,
docket_id TEXT REFERENCES dockets(id),
title TEXT,
document_type TEXT,
subtype TEXT,
posted_date TEXT,
posted_year INTEGER,
posted_month INTEGER,
comment_start_date TEXT,
comment_end_date TEXT,
last_modified TEXT,
fr_doc_num TEXT,
open_for_comment INTEGER,
withdrawn INTEGER,
object_id TEXT
);
CREATE INDEX idx_docs_agency ON documents(agency_id);
CREATE INDEX idx_docs_docket ON documents(docket_id);
CREATE INDEX idx_docs_date ON documents(posted_date);
CREATE INDEX idx_docs_year ON documents(posted_year);
CREATE INDEX idx_docs_type ON documents(document_type);
CREATE INDEX idx_docs_frnum ON documents(fr_doc_num);
CREATE INDEX idx_docs_comment_end ON documents(comment_end_date) WHERE comment_end_date IS NOT NULL AND withdrawn = 0;