Complying with the unique device identifier (UDI) system requirements is a critical milestone for medical device manufacturers, distributors, and end users. Ensuring compliance is not just about meeting a regulatory deadline; it's about safeguarding the integrity and safety of medical devices throughout their lifecycle in Europe and the United States.

Our comprehensive whitepaper, "Ready for the UDI Mandate Deadline?" dives into the intricacies of UDI implementation, shedding light on the complexities beyond the surface. The ultimate goal is clear – to effectively identify and trace medical devices, from a simple bedpan to a lifesaving artificial heart, promoting safety across the healthcare landscape.

However, the journey towards UDI compliance goes beyond merely affixing a printed barcode to a package. Establishing a robust system for verifying UDI markings, and ideally automating these processes, requires a thorough understanding of the means and methods involved. Inline verification during label generation and off-line validation in active service are pivotal components of a successful UDI system.

In this whitepaper, we not only outline the UDI labeling requirements but also provide actionable insights into best practices. Discover how the medical device industry can ensure that marking methods are not only compliant but also meticulously verifiable. Elevate your understanding of UDI implementation and gain confidence in navigating the intricacies of the mandate.

Don't miss out on this opportunity to empower your organisation with the knowledge needed to thrive in the era of UDI compliance. Download our whitepaper now to stay ahead in the evolving landscape of medical device regulations.