How to meet Unique Device Identification (UDI) requirements

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The term UDI is used increasingly in healthcare, so understanding what it means and how to meet the regulatory requirements for identification and physical marking of products.

This webinar will provide insight to what UDI means; how to achieve unique device/product identification with GS1 standards; how this can be used not only for international regulatory compliance (US FDA etc.) but also to meet the needs of local industry; and provide guidance to where to find more information to support your project. Included also are considerations related to your product packaging and options with regards to data carriers (linear and 2D barcodes).

The target audience for this webinar are manufacturers, distributors or solution providers who need to understand these requirements.

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