Navigating the UDI Final Rule

Unique Device Identifier – also known as "UDI" – is a new FDA labeling requirement for medical device manufacturers designed to track devices in the interest of public safety. Manufacturers that have seen UDI coming and have taken actions to prepare for its implementation will find UDI manageable; for those who have not, UDI might seem like the light of an oncoming train.

Read about this new labeling requirement, how much time manufacturers have to implement it, and an overview of how labeling requirements are going to change.

Click here to  access the article.

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