UDI is fast approaching. Stay on track with deadlines and requirements!

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We can help you understand the production implications of the 2016 deadline and identify the ideal direct marking solution for your products. Download our infographic to learn more about UDI and contact us for more information, sample marking and application consulting!

Unique Device Identification: Get to know UDI! 

UDI is a unique device identification system created and regulated by the Food and Drug Administration (FDA). It is designed to adequately identify medical devices through their distribution and use. When fully implemented, most medical devices will include a unique device identifier in human and machine-readable forms. When required, these identifiers must not only appear on labels and packaging, but on the devices themselves as in the case of repeatedly used equipment (i.e. surgical tools, instruments) which has to be marked directly.

This summary is for informational purposes only and is not intended as legal advice. For a complete description of the Unique Device Identification system, go to: www.fda.gov

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