2024年12月17日 · The Global Unique Device Identification Database (GUDID) is a database administered by the FDA that serves as a reference catalog for every device with a unique …

2023年8月21日 · 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. You …

By using this system, you understand and consent to the following: - The Government may monitor, record, and audit your system usage, including usage of personal devices and email …

In collaboration with the National Library of Medicine, the FDA has created a portal, called AccessGUDID, to make device identification information in the GUDID available for...

2024年12月17日 · Provides information necessary for submitting data to the Global Unique Device Identification Database (GUDID). Primarily intended for device labelers.

Note: Quick Search only applies to Device Identifiers, Company Name, Brand Name, GMDN Preferred Term Name, and Model Number. Please use 'Advanced Search' to search using …

2023年12月13日 · 通过GUDID，FDA就可以实现产品从制造、到经销、再到医疗机构使用的可追溯性。 因为只有制造商或标签商注册GUDID账号才有权限进入数据库，为了方便大众、研究 …

The Global Unique Device Identification Database (GUDID) contains key device identification information submitted to the FDA about medical devices that have Unique Device Identifiers …

Over the past year, FDA designed and developed the Global Unique Device Identification Database (GUDID) to prepare for the implementation of the UDI final rule. The GUDID is a …

2024年12月17日 · Device labelers have two options for submitting GUDID data: the GUDID web application and HL7 SPL file submission using the FDA Electronic Submission Gateway.