HaRi
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Data sources

We refresh every regulatory source on a published cadence. This page shows when each source was last updated and how often it refreshes.

US (FDA)

  • FDA 510(k) clearances
    Pre-market device clearance decisions and product details from the FDA 510(k) database.
    Update due
    Fortnightly 46 days ago
  • FDA device recalls
    Recall notices and corrective actions issued for FDA-regulated medical devices.
    Update due
    Fortnightly 31 days ago
  • FDA MAUDE adverse events
    Adverse event reports submitted to the FDA's Manufacturer and User Facility Device Experience database.
    Update due
    Fortnightly 31 days ago
  • FDA 510(k) summaries
    Structured data extracted from FDA 510(k) summary PDFs — predicate devices, performance standards, and indications for use.
    Update due
    Fortnightly 31 days ago
  • FDA product codes
    FDA product-code definitions, device classes, and regulation references used to categorise medical devices.
    Update due
    Fortnightly 31 days ago
  • FDA UDI database
    Unique Device Identifier records published in the FDA Global UDI Database (GUDID).
    Update due
    Fortnightly 31 days ago
  • FDA AI/ML device list
    Devices the FDA publishes on its list of AI/ML-enabled medical devices.
    Update due
    Fortnightly 44 days ago
  • FDA AR/VR device list
    Devices the FDA publishes on its list of augmented- and virtual-reality medical devices.
    Update due
    Fortnightly 44 days ago
  • FDA sensor-based device list
    Devices the FDA publishes on its list of sensor-based medical devices.
    Update due
    Fortnightly 44 days ago

UK (MHRA)

  • MHRA device registrations
    Medical device registrations from the UK Medicines and Healthcare products Regulatory Agency.
    Update due
    Fortnightly 31 days ago
  • MHRA manufacturers
    Manufacturer addresses, contact details, and UK Responsible Person designations from the MHRA registry.
    Update due
    Fortnightly 31 days ago
  • MHRA products
    Individual product entries (brand and trade names) attached to MHRA device registrations.
    Update due
    Fortnightly 31 days ago
  • MHRA Field Safety Notices
    Manufacturer-issued Field Safety Notices published by the MHRA covering corrective actions and product alerts.
    Update due
    Fortnightly 46 days ago
  • UK ICO registrations
    Data-protection registrations published by the UK Information Commissioner's Office (ICO).
    Update due
    Fortnightly 31 days ago

EU (EUDAMED)

  • EUDAMED devices
    UDI-DI device records from the European Database on Medical Devices, including BUDI version history.
    Update due
    Fortnightly 46 days ago
  • EUDAMED actors
    Manufacturer and authorised-representative actor records (SRN, contact details, PRRC) from EUDAMED.
    Update due
    Fortnightly 46 days ago
  • EUDAMED certificates
    Notified Body certificate records from the EUDAMED NB&C module, including certificate number, status, issuing notified body, and the Basic UDI-DIs each certificate covers.
    Update due
    Fortnightly 31 days ago

Canada (Health Canada)

  • Health Canada MDALL licences
    Active medical device licences from Health Canada's Medical Devices Active Licence Listing (MDALL).
    Update due
    Fortnightly 31 days ago
  • Health Canada incidents
    Mandatory problem reports and incident summaries published by Health Canada for medical devices.
    Update due
    Fortnightly 31 days ago

AU (TGA)

  • TGA ARTG entries
    Medical device entries from the Australian Register of Therapeutic Goods, including sponsor and manufacturer.
    Update due
    Fortnightly 31 days ago

How we measure freshness. A source shows Update due when its next refresh is later than the usual cadence window (allowing a small grace buffer). Existing data remains available and unchanged while a refresh is pending. Timestamps reflect when our pipeline finished ingesting the latest snapshot.

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