Product group In-vitro diagnostics - instruments, apparatuses and systems
Reference 54533/25

Product group Active implantable medical devices - programming and control equipment
Reference 55467/25

Product group Electromedical fields - equipment for MR tomography
Reference 55530/25

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 56076/25

Product group In-vitro diagnostics - immunological products
Reference 54149/25

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 55737/25

Product group Radiotherapy / Radiation protection - nuclear medical therapeutic equipment
Reference 55754/25

Product group Non-active implants - special implants
Reference 54077/25

Product group Orthopaedic / Rehabilitation technology - mobility aids
Reference 54382/25

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 55568/25

Product group Physical therapy - inhalation therapy
Reference 51035/25

State: October 2025

On the following page you will find the figures of marketable medicinal products in the responsibility of the BfArM, broken down according to type of authorisation procedure as well as details of the authorisation status. The figures are updated on a monthly basis.

Here the BfArM publishes the current processing statistics of authorisations and registrations as well as of renewals. The figures are updated on a monthly basis.

Product group Non-active implants - bone surgery
Reference 54282/25

Product group In-vitro diagnostics - instruments, apparatuses and systems
Reference 52062/25

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 54395/25

Pursuant to the Regulations (EU) 2017/745 and (EU) 2017/746 (MDR and IVDR) as well as German national regulations a favourable opinion of the competent ethics committee and an approval of or notification to the competent authority is required in order to perform a clinical investigation / performance study for medical devices.

With its barrier-free (according to BITV, German Barrier-free Information Technology Ordinance), graphical user interface the German Medical Devices Information and Database System (Deutsches Medizinprodukte-Informations-und Datenbanksystem, DMIDS) contributes to the market surveillance of medical devices in Germany.

Active substance: promethazine The BfArM informs that the use of medicines containing promethazine is contraindicated in children under the age of 6 due to age-specific risks.