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NLM AccessGUDID — Device Identity (FDA Global UDI Database)
The identity registry for every marketed medical device by its unique device identifier: brand, model, catalog number, maker, and safety attributes like single-use, sterile, and MRI compatibility.
What Vlada adds: Preserves the publisher data, normalizes schema eras and identifiers, and connects the product to compatible healthcare entities with measured join coverage.
- rows
- 5.1M
- rows
- datasets
- 1
- datasets
- cadence
- derived
- cadence
- coverage
- 2026
- coverage
Publishers: U.S. Food and Drug Administration · National Library of Medicine
What's inside
Primary dataset
The FDA Global UDI Database (via NLM AccessGUDID) — every marketed medical device by its Device Identifier (PrimaryDI): brand, version/model, catalog number, company (DUNS), description, commercial-distribution status, and flags (single-use, sterile, MRI safety, Rx/OTC, kit, combination product).
grain: One row per device (release_month, PrimaryDI) — brand/model/company + flags.
5.1M rows