EU IVDR In Vitro Diagnostic Devices

View 10000 EU IVDR in vitro diagnostic devices on BEUDAMED, the Better Database on Medical Devices. This searchable index aggregates device listings, manufacturer details, and declared regulatory status for IVDs governed by the EU In Vitro Diagnostic Regulation (IVDR). Find device types ranging from reagents and calibrators to instrument platforms and companion diagnostics across all IVDR risk classes.

The EU IVDR introduced stricter requirements for performance and clinical evidence, increased notified body involvement, and expanded post-market surveillance obligations for in vitro diagnostics. Use BEUDAMED data to compare conformity routes, UDI assignments, and vigilance records to support procurement, regulatory compliance checks, and market surveillance activities.