{"service":"agent-device-verify","description":"Pay-per-call medical-device risk cards for AI agents (x402). POST /verify with a UDI/DI, brand, or labeler company; pay $0.08 in USDC on Base per call. Returns the GUDID labeler record, MR-safety status, GUDID-cited premarket submission signal, a live openFDA recall cross-reference, and an explainable risk level.","payment":{"protocol":"x402 v2","network":"eip155:8453","price_per_call":"$0.08","mode":"mainnet"},"data_source":"FDA GUDID (AccessGUDID) monthly full release, federal public domain; openFDA device enforcement (live)","endpoints":{"POST /verify":"{udi?: string, brand?: string, company?: string} - UDI/DI, brand name, or labeler company","GET /coverage":"index coverage + build info","GET /openapi.json":"OpenAPI 3.1 document","GET /.well-known/x402":"x402 resource manifest"},"related":"For a 510(k) clearance verdict by K-number or device name, see device-clearance-verify. This service returns the GUDID record's own premarket citation as a signal, not a verdict.","disclaimer":"Informational only, not legal, regulatory, or clinical advice. GUDID records are labeler-submitted and may lag corrections or contain labeler errors. An MR-safety status is device- and configuration-specific — always confirm against the device's current labeling before any MRI exposure decision. Recall data is drawn live from openFDA device enforcement reports and may not capture every field action. A 510(k) submission number present in a GUDID record indicates the labeler cited a premarket submission — it is not, by itself, a clearance verdict (for verdicts see device-clearance-verify). Verify critical information against FDA sources."}