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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).
Last updated 4h ago
On-chain USDC settlements received on Base · 0x329b4b66AFBC407bb3a22DAEb465487c6FAa08C1
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