Composite medical-device risk card from a UDI device identifier (DI), brand, or labeler company. Returns the GUDID labeler record (brand, company, GMDN term, version/model, catalog number), MR-safety status, GUDID-cited premarket submission signal, a live openFDA recall cross-reference for the labeler, and an explainable risk level. FDA GUDID data (public domain).
https://agent-device-verify.iykykblog.workers.dev/verify