The world of medical devices is often described as one of the most unique industries. And while some may groan at the mention of regulatory requirements, those committed to True Quality know that they are essential to ensuring patient safety and the responsible manufacturing of medical devices.

Among these regulations is the FDA’s Unique Device Identification (UDI) system. UDIs are unique strings of numbers, letters and special characters that are used to identify a specific piece of medical equipment. UDIs are encoded in barcodes and can be scanned using a universal medical device data model (UMDDM). They can also be uploaded to the FDA’s global UDI database.

Track Unique Device Patterns for User Identification

As such, identify unique device patterns allow hospitals and other healthcare organizations to more easily locate devices in their inventory. This helps speed up the recall process and reduces medical errors, as well as allowing them to integrate standardized device information into their electronic health records.

Additionally, UDIs allow manufacturers to better track and monitor their products by providing them with an accessible record of a product’s location and history. They can use this data to detect and resolve issues and improve their manufacturing processes.

In addition, UDIs can provide valuable insights to marketers and publishers looking to understand how their campaigns are performing. By leveraging the device ID and combining it with geolocation and session tracking, marketers can gain a deeper understanding of their audience’s behaviors across all devices. This enables them to better optimize and optimize their content, campaigns, and user experience.