Gudid Login

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Last updated at November 10th, 2020

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Login to GUDID

https://gudid.fda.gov/gudid/login

U.S. Food and Drug Administration 10903 New Hampshire Ave. Silver Spring, MD 20993 · 1-888-INFO-FDA (1-888-463-6332)

Status : Online

AccessGUDID - Identify Your Medical Device

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

The Global Unique Device Identification Database (GUDID) contains key device identification information submitted to the FDA about medical devices that have Unique Device Identifiers (UDI).. The FDA is establishing the unique device identification system to adequately identify devices sold in the U.S.- from manufacturing through distribution to patient use.

Status : Online

Welcome to GUDID

https://gudid.fda.gov/gudid/app/main.xhtml

U.S. Food and Drug Administration 10903 New Hampshire Ave. Silver Spring, MD 20993 · 1-888-INFO-FDA (1-888-463-6332)

Status : Online

AccessGUDID (for the public) | FDA

https://www.fda.gov/medical-devices/global-unique-device-identification-database-gudid/accessgudid-public

In collaboration with NLM, the FDA has created a portal, called AccessGUDID, to make device identification information in the GUDID available for everyone.

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Global Unique Device Identification Database (GUDID) | FDA

https://www.fda.gov/medical-devices/unique-device-identification-system-udi-system/global-unique-device-identification-database-gudid

The Global Unique Device Identification Database (GUDID) is a database administered by the FDA that will serve as a reference catalog for every device with a unique device identifier (UDI).

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AccessGUDID - ABOUT AccessGUDID

https://accessgudid.nlm.nih.gov/about-gudid

About GUDID. 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.

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Submit Data to GUDID | FDA

https://www.fda.gov/medical-devices/global-unique-device-identification-database-gudid/submit-data-gudid

The GUDID web application is an online application for submitting GUDID data. Before you use the GUDID web application, read these user manuals: GUDID User Manual (PDF – 2.2MB)

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Request a GUDID Account | FDA

https://www.fda.gov/medical-devices/global-unique-device-identification-database-gudid/request-gudid-account

Step 2: Complete the GUDID New Account Request. After you submit the GUDID New Account inquiry, the FDA UDI Help Desk will email you the GUDID New Account Request document in a fillable PDF format.

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Global Unique Device Identification Database (GUDID)

https://gudid.fda.gov/gudid/app/help/GUDIDUserManual.pdf

From this page you can login, search, among other functions among other functions as described in this document. Login Screen From the GUDID log in screen, enter your username and pasword for account management or data entry. Please review the System User Agreement prior to logging into the GUDID.

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Log in - GMDN Agency

https://www.gmdnagency.org/Account/Login

Provide your account credentials. Log in Provide your account credentials. Email

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