Coverage
Every device, mapped.
MedevIQ reconciles India's medical-device record — every CDSCO-licensed manufacturer, importer, and device licence — against the global one of FDA clearances, EUDAMED registrations, and worldwide adverse-event reports. This page lists what's in the canonical layer today, where the data comes from, and where we are still building out.
What's covered per record
Where the data comes from
REGULATORS
CDSCO Indian licensing · US FDA (510(k), PMA, De Novo) · EUDAMED EU registrations · Health Canada MDL · TGA ARTG · PMDA · MHRA · NMPA
STANDARDS
GMDN Global Medical Device Nomenclature · UMDNS · HSN Indian customs classification · BIS Indian standards
SAFETY
FDA MAUDE US adverse-event reports · EUDAMED FSCA EU field-safety corrective actions · Health Canada incidents · FDA recalls
Active investment areas
MedevIQ launched as an AI-reviewed canonical layer with deep India and US coverage. The following areas are where we are continuously densifying the record. Per-area completion rates published at v1 launch.
Device ↔ drug canonical bridge
Joining every device-maker to its drug portfolio via the canonical company entity, enabling cross-rail queries (device + drug from the same manufacturer).
Hospital formulary depth
Expanding the device ↔ procurement-tier mapping with INR cost references for Indian hospital workflows.
EUDAMED density
EU UDI-DI records grow as more manufacturers complete EUDAMED registration; we mirror the public surface as it densifies.
Clinical evidence layer
Comparator-device evidence, indications and contraindications mapped against authoritative regulatory submissions.
Refresh cadence