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What is u d i?
UDI stands for Unique Device Identification, it is a system used to uniquely identify medical devices distributed in the United States.
Who is required to file u d i?
Manufacturers of medical devices are required to file UDI.
How to fill out u d i?
UDI is typically filled out using an FDA-accredited issuing agency's database.
What is the purpose of u d i?
The purpose of UDI is to improve patient safety, facilitate medical device recalls, and enhance post-market surveillance.
What information must be reported on u d i?
UDI must include device identifiers, production identifiers, and if applicable, a lot number and expiration date.
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