databases > DOI:10.25504/FAIRsharing.ennep4

ready 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.




How to cite this record FAIRsharing.org: GUDID; Global Unique Device Identification Database; DOI: https://doi.org/10.25504/FAIRsharing.ennep4; Last edited: Feb. 22, 2018, 3 p.m.; Last accessed: Sep 20 2018 9:30 p.m.


Record added: April 10, 2016, 10:22 a.m.
Record updated: Feb. 22, 2018, 3 p.m. by The FAIRsharing Team.








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.


Fed Regist 2013

View Paper (PubMed)

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