Global Unique Device Identification Database

Abbreviation:GUDID

General Information

The Global Unique Device Identification Database (GUDID - pronounced "Good ID") is a database administered by the FDA as part of the UDI system. The GUDID contains device identification information submitted by device companies to the FDA. The GUDID contains ONLY the Device Identifier (DI), which serves as the primary key to obtain information in the database. Production Identifiers (PI) are not submitted to or stored in the GUDID, but GUDID data indicates which PIs are on the device label. Many data elements in the GUDID correspond to information on the medical device label. The figure below shows a fictitious medical device label and identifies the GUDID data elements that appear on the label. Please refer to the FDA UDI website for more information about GUDID data elements.

Homepage https://accessgudid.nlm.nih.gov/

Countries that developed this resource United States

Created in 2016

Taxonomic range

Homo sapiens

Knowledge Domains

Subjects

How to cite this record FAIRsharing.org: GUDID; Global Unique Device Identification Database; DOI: https://doi.org/10.25504/FAIRsharing.ennep4; Last edited: March 19, 2021, 12:38 p.m.; Last accessed: Apr 11 2021 3:04 a.m.

Record added: April 10, 2016, 10:22 a.m.
Record updated: Feb. 23, 2021, 10:48 a.m. by The FAIRsharing Team.

Show edit history

Edits to 'https://fairsharing.org/FAIRsharing.ennep4' by 'The FAIRsharing Team' at 10:48, 23 Feb 2021 (approved):

	'organizations' has been modified:
		Before:
			US Food and Drug Administration (FDA)|http://www.fda.gov/|Funds
			US Food and Drug Administration (FDA)|http://www.fda.gov/|Maintains
		After:
			US Food and Drug Administration (FDA)|http://www.fda.gov/|Maintains,Funds
		Added:
			US Food and Drug Administration (FDA)|http://www.fda.gov/|Maintains,Funds
		Removed:
			US Food and Drug Administration (FDA)|http://www.fda.gov/|Funds
			US Food and Drug Administration (FDA)|http://www.fda.gov/|Maintains

	'contact' has been modified:
		Before: FDA UDI
		After: 

	'miriam_id' has been modified:
		Before: None
		After: 

	'publications' has been modified:
		Before:
			Unique device identifiers for coronary stent postmarket surveillance and research: a report from the Food and Drug Administration Medical Device Epidemiology Network Unique Device Identifier demonstration.|Tcheng JE,Crowley J,Tomes M,Reed TL,Dudas JM,Thompson KP,Garratt KN,Drozda JP Jr|Am Heart J|2014
			Unique device identification system. Final rule.||Fed Regist|2013
		After:
			Unique device identifiers for coronary stent postmarket surveillance and research: a report from the Food and Drug Administration Medical Device Epidemiology Network Unique Device Identifier demonstration.|Tcheng JE,Crowley J,Tomes M,Reed TL,Dudas JM,Thompson KP,Garratt KN,Drozda JP Jr|Am Heart J|2014
			Unique device identification system. Final rule.|Food and Drug Administration, HHS|Fed Regist|2013
		Added:
			Unique device identification system. Final rule.|Food and Drug Administration, HHS|Fed Regist|2013
		Removed:
			Unique device identification system. Final rule.||Fed Regist|2013

In Collections

RDA Covid-19 WG Resources

eTRIKS Standards Starter Pack

Support

General

contact form	https://support.nlm.nih.gov/ics/support/ ...
help	https://accessgudid.nlm.nih.gov/help/sea ...
help	https://accessgudid.nlm.nih.gov/help/hom ...
rss	http://accessgudid.nlm.nih.gov/resources ...
schema file	https://accessgudid.nlm.nih.gov/release_ ...

Tools

Advanced Search

https://accessgudid.nlm.nih.gov/advanced-search

Access / Retrieve Data

Conditions of Use

Data Access

Release

https://accessgudid.nlm.nih.gov/download

REST Web Services

GET /devices/implantable/list	https://accessgudid.nlm.nih.gov/resources/developers/implant_list_api
GET /devices/lookup	https://accessgudid.nlm.nih.gov/resources/developers/device_lookup_api
GET /parse_udi	https://accessgudid.nlm.nih.gov/resources/developers/parse_udi_api
GET /devices/implantable/download	https://accessgudid.nlm.nih.gov/resources/developers/implant_list_down ...

Publications

Unique device identifiers for coronary stent postmarket surveillance and research: a report from the Food and Drug Administration Medical Device Epidemiology Network Unique Device Identifier demonstration.

Tcheng JE,Crowley J,Tomes M,Reed TL,Dudas JM,Thompson KP,Garratt KN,Drozda JP Jr
Am Heart J 2014

View Paper (PubMed) View Publication

Unique device identification system. Final rule.

Food and Drug Administration, HHS
Fed Regist 2013

View Paper (PubMed)

Related Standards

Reporting Guidelines

No guidelines defined

Terminology Artifacts

Health Level Seven Reference Implementation Model

Models and Formats

No syntax standards defined

Identifier Schemas

No identifier schema standards defined

Metrics

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Related Databases

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This record is not implemented by any policy.

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Funds

US Food and Drug Administration (FDA) (Government body)

Maintains

US Food and Drug Administration (FDA) (Government body)

Global Unique Device Identification Database

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