EU IVDR Medical Devices from Germany

View 3640 EU IVDR medical devices from Germany on BEUDAMED, the Better Database on Medical Devices. These listings cover in vitro diagnostic devices regulated under the EU In Vitro Diagnostic Regulation (IVDR) and reflect the stricter conformity and performance requirements that replaced the IVDD. Device entries include key details such as device type, manufacturer, regulatory status and intended use to support regulatory review and purchasing decisions.

German IVDR devices commonly require notified body involvement, robust performance and clinical evidence, and Unique Device Identification (UDI) before placement on the EU market. BEUDAMED helps users compare device performance claims, conformity assessment routes, and available post-market surveillance information to support regulatory, clinical, and procurement workflows.