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Responsible for the service Finnish Medicines Agency Fimea

Manufacturer’s notification form for interruption or discontinuation of deliveries

  • Printable form

Manufacturer notifies:

  • the competent authority of the Member State in which the manufacturer or its authorised representative is established;
  • economic operators; and
  • health care units and health care professionals to whom it supplies devices directly.

The manufacturer reports the information to the competent authority using the form MDCG 2024-16. The information is submitted to Fimea by em ...

Form

Delivery details for the form

The information is submitted to Fimea by email: laiteinfo@fimea.fi or registry@fimea.fi.

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Text edited by: Finnish Medicines Agency Fimea
Updated: 2/1/2026