Two men sit at a table with a laptop, discussing a dmids document. One man is holding glasses while the other looks focused. A blurred person is visible in the background near a window with greenery outside.

What Is DMIDS? The "German Medical Device Information and Database System" Explained

The German Medical Device Information and Database System (DMIDS: Deutsches Medizinprodukte-Informations- und Datenbanksystem) is a database administered by the Federal Institute for Drugs and Medical Devices (BfArM: Bundesinstitut für Arzneimittel und Medizinprodukte). It provides a digital platform for data exchange between authorities and other stakeholders such as ethics committees, manufacturers, EU representatives, and Notified Bodies.

DMIDS is used, among other things, for:

  • Registration of manufacturers and authorised representatives
  • Registration of medical devices and IVDs
  • Submission and management of clinical investigations and performance studies (MDR/IVDR)
  • Management of contact information and project-related correspondence


Note:

DMIDS supports national processes in Germany and serves as a complement to – and interim solution alongside – European IT systems such as EUDAMED. As the mandatory use of EUDAMED modules is phased in, certain reporting obligations will progressively transfer to EUDAMED.

Need support navigating DMIDS? Get in touch – we are happy to help.

Dr Nina Miljanovic Jovanovic, Senior Study Manager

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BfArM: Federal Institute for Drugs and Medical Devices

DMIDS: German Medical Device Information and Database System

EU: European Union

EUDAMED: European Database on Medical Devices

IVDs: In vitro diagnostics

IVDR: In Vitro Diagnostic Regulation

MDR: Medical Device Regulation