UDI is coming, are you ready?


The FDA has established a unique identification system {UDI} to adequately identify medical devices through their distribution and use. This new system requires that most medical device labels include a unique device identifier. As of September 23, 2016 the FDA will require compliance by all Class II device manufacturers. Are you ready? If not… don’t worry because we are! Give us a call today at 1.800.433.7797 and find out how we can help you.

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