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Data sources

We re-scrape every regulatory source on a published cadence. This page shows when each source was last successfully refreshed, and flags any that have fallen behind.

US (FDA)

  • FDA 510(k) clearances
    Pre-market device clearance decisions and product details from the FDA 510(k) database.
    Behind schedule
    Weekly Not yet imported
  • FDA device recalls
    Recall notices and corrective actions issued for FDA-regulated medical devices.
    Behind schedule
    Weekly Not yet imported
  • FDA MAUDE adverse events
    Adverse event reports submitted to the FDA's Manufacturer and User Facility Device Experience database.
    Behind schedule
    Weekly Not yet imported
  • FDA 510(k) summaries
    Structured data extracted from FDA 510(k) summary PDFs — predicate devices, performance standards, and indications for use.
    Behind schedule
    Weekly Not yet imported
  • FDA product codes
    FDA product-code definitions, device classes, and regulation references used to categorise medical devices.
    Behind schedule
    Weekly Not yet imported
  • FDA UDI database
    Unique Device Identifier records published in the FDA Global UDI Database (GUDID).
    Behind schedule
    Weekly Not yet imported

UK (MHRA)

  • MHRA device registrations
    Medical device registrations from the UK Medicines and Healthcare products Regulatory Agency.
    Behind schedule
    Weekly Not yet imported
  • MHRA manufacturers
    Manufacturer addresses, contact details, and UK Responsible Person designations from the MHRA registry.
    Behind schedule
    Weekly Not yet imported
  • MHRA products
    Individual product entries (brand and trade names) attached to MHRA device registrations.
    Behind schedule
    Weekly Not yet imported
  • MHRA Field Safety Notices
    Manufacturer-issued Field Safety Notices published by the MHRA covering corrective actions and product alerts.
    Behind schedule
    Weekly Not yet imported
  • UK ICO registrations
    Data-protection registrations published by the UK Information Commissioner's Office (ICO).
    Behind schedule
    Weekly Not yet imported

EU (EUDAMED)

  • EUDAMED devices
    UDI-DI device records from the European Database on Medical Devices, including BUDI version history.
    Behind schedule
    Weekly Not yet imported
  • EUDAMED actors
    Manufacturer and authorised-representative actor records (SRN, contact details, PRRC) from EUDAMED.
    Behind schedule
    Weekly Not yet imported

Canada (Health Canada)

  • Health Canada MDALL licences
    Active medical device licences from Health Canada's Medical Devices Active Licence Listing (MDALL).
    Behind schedule
    Weekly Not yet imported
  • Health Canada incidents
    Mandatory problem reports and incident summaries published by Health Canada for medical devices.
    Behind schedule
    Weekly Not yet imported

AU (TGA)

  • TGA ARTG entries
    Medical device entries from the Australian Register of Therapeutic Goods, including sponsor and manufacturer.
    Behind schedule
    Weekly Not yet imported

How we measure freshness. A source is marked Behind schedule if we haven't completed a successful scrape within its committed cadence window (plus a small grace buffer to avoid flagging normal-late runs). Timestamps reflect the wall-clock time our pipeline finished ingesting the latest snapshot.

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