Story perspectives

UK Launches Consultation for Indefinite CE-Marked Device Recognition

2/20/2026

Summary

Story summary

The UK’s Medicines and Healthcare products Regulatory Agency (MHRA) has launched a consultation on indefinite recognition of CE-marked medical devices to improve patient access and ensure a reliable supply of safe technologies.
This consultation will remain open until April 10, 2026, and seeks feedback on three proposals regarding transitional arrangements and recognition of compliant devices.
These initiatives support the UK’s objective to become a leading MedTech market by 2030 and address industry demands for regulatory certainty.

History

Historical Context

Established in 1993, the CE marking system ensures product safety across the European Union, allowing compliant goods to be traded freely within the European Economic Area. The UK's Medicines and Healthcare products Regulatory Agency (MHRA) is currently consulting on CE-marked medical devices, aiming to enhance patient access and solidify the UK’s position as a leading MedTech market by 2030.

1 of 2

Story summary

The UK’s Medicines and Healthcare products Regulatory Agency (MHRA) has launched a consultation on indefinite recognition of CE-marked medical devices to improve patient access and ensure a reliable supply of safe technologies.
This consultation will remain open until April 10, 2026, and seeks feedback on three proposals regarding transitional arrangements and recognition of compliant devices.
These initiatives support the UK’s objective to become a leading MedTech market by 2030 and address industry demands for regulatory certainty.

1 / 2