VerifyDI

VerifyDI scans the Unique Device Identifier (UDI) on a medical device label and tells clinical staff, at a glance, whether the device is expired, nearing expiration, or subject to an FDA recall. Point the camera at a device label. VerifyDI reads the GS1 or HIBC barcode, extracts the device identifier, lot, serial number, and expiration date, and shows a clear status before the device reaches the patient. Recall Checking • Every scan is checked against FDA recall data curated by VerifyDI • Recalls are matched by device identifier, and by lot, serial number, or date range when a recall is limited to specific units • A recalled device shows a red status and an alert vibration • Recall details show what was matched and link to the recall notice • Each clear result shows the date of the recall data it was checked against • The recall check runs on the device and keeps working without a network connection Expiration Checking • Instant status for expired devices and devices nearing expiration • Configurable warning thresholds for approaching expiration • Reads expiration dates from barcodes, and from printed label text when the date isn’t encoded in the barcode Built for Clinical Workflows • Supports GS1 and HIBC barcode formats, including labels that split device data across multiple barcodes • Scans several barcodes in the frame at once and shows the most urgent result • Designed for supply rooms, OR prep, and point-of-use verification For Healthcare Organizations VerifyDI is intended for hospitals, surgical centers, and other healthcare organizations. It helps reduce the risk of using expired or recalled devices and supports existing safety and compliance processes. It does not replace your organization’s recall management procedures. Access Requirements VerifyDI is available to authorized users whose organizations have an active account. User access is managed by your organization.