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