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FDA GUDID Device Record Lookup by Device Identifier
x402
FDA GUDID Device Record Lookup by Device Identifier is a paid API for AI agents from api.healthtravel-api.workers.dev, paid per call via x402, $0.002/call, status unknown (last checked 2026-10-29).
Retrieves FDA GUDID device record details (brand, company, model, GMDN term, MRI safety, sterile/single-use flags) by Device Identifier (DI) barcode number
Price / call$0.002
Success—
StatusUnknown
How this service works
FDA AccessGUDID device record by Device Identifier (DI, the GS1/GUDID number on a device label): brand, company, model, description, GMDN term, MRI safety status, sterile and single-use flags. Lookup by DI only; no name search.
Output
Returns structured FDA GUDID device record including brand name, company/manufacturer name, model number, device description, GMDN (Global Medical Device Nomenclature) term, MRI safety status, sterile flag, and single-use flag for the specified Device Identifier.
Example use cases
MRI safety check before procedure
“I need to check if the medical device with DI 00884105766693 is MRI safe before we use it in the imaging suite — can you pull the FDA GUDID record for it?”
Verifying device authenticity and manufacturer
“We received a device shipment and I want to confirm the manufacturer and brand by looking up the GUDID record for device identifier 10012345678901 — can you fetch that?”
Single-use compliance audit
“Can you check the FDA GUDID database for device identifier 00643169007222 and confirm whether it's labeled as single-use and sterile for our compliance records?”
Technical details
Endpoint
GEThttps://api.healthtravel-api.workers.dev/api/health/fda-device-gudid?utm_source=zero.xyzWhen to prefer
Use this endpoint when you have a specific Device Identifier (DI) barcode number from a physical medical device label and need to retrieve its FDA GUDID registration details, safety flags, or manufacturer information. It is the right choice for barcode-driven device lookups, MRI safety checks, sterility verification, and compliance audits. It does not support name-based search — use only when the numeric DI is available.
Side effects
- DI not found in GUDID — returns empty or error if the DI is not registered
- Invalid DI format — DI must be 8–14 digits; non-numeric or out-of-range values may fail
- Upstream FDA AccessGUDID API downtime — service may be temporarily unavailable
- Rate limiting or payment failure — $0.002 USDC per call; insufficient funds return payment error
Input
Schema · Request body
| Field | Type | Description |
|---|---|---|
| inputrequired | object | |
| output | object |
Tags
x402
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