Exceptional Use Authorisation
Download this document free
Get this document with your free trial. Choose from the full Complyzard library.
Try 1 month free30 days free, then $19/month. Trial terms apply. Card required. Cancel anytime.Document information
How to apply for an exceptional use authorisation to place medical devices on the UK market.
Adapted edition
- Document type
- Reference Guide
- Format
- DOCX
- Pages
- 4
- Language
- English
- Version
- 1.0
- Updated
- 2026-09-17
- Category
- Safety & operations
- Licence
- Open Government Licence v3.0
Description
How to apply for an exceptional use authorisation to place medical devices on the UK market. Consult the original guidance for current legal and operational details.
Contents
- Great Britain (England, Scotland and Wales)
- Northern Ireland
- Requirements under EUA
- How to Apply for an EUA in Great Britain and Northern Ireland
- Assessment steps of EUA applications for Great Britain and Northern Ireland
- Outcome reporting
- Complaints
- Reviews
Source and licence
Medicines and Healthcare products Regulatory Agency
AttributionMedicines and Healthcare products Regulatory Agency, ‘Exceptional Use Authorisation’ (updated 31 March 2025), reused under the Open Government Licence v3.0.
ChangesNeutral text-only adaptation from the official GOV.UK Content API body: headings, paragraphs, ordered and unordered list items and clickable source-link destinations in an appendix preserved. Images, logos, page design, accessible-format request widgets and linked attachments excluded; normalised whitespace, invisible format marks and typography.
Version history
- v1.017/09/2026