UKCA (UK Conformity Assessed) is an independent local product conformity assessment mark established by the UK after Brexit, separating from the EU CE system. It was officially launched on 1 January 2021.

Key Reminder: For non UK manufacturers, whether using CE or UKCA marking, a UK Responsible Person (UKRP) must be appointed. The UKRP is responsible for regulatory liaison and technical file retention. This is a mandatory requirement for customs clearance and market surveillance.
Most Industrial Goods: CE / UKCA Dual Track System, No Mandatory Cut off Date
Covered categories: Electrical & electronic goods, toys, general machinery, Personal Protective Equipment (PPE), furniture, hardware tools, low voltage equipment and more than 20 mainstream consumer product categories.
Policy basis: The UK Product Safety and Metrology etc. (Amendment) Regulations 2024 came into force on 1 October 2024. It formally removed the statutory expiry date for CE marking across 21 product sectors.
Current status:
· Products bearing CE marking can be customs cleared and sold in Great Britain indefinitely.
· Enterprises may freely choose CE or UKCA marking based on customer requirements and corporate compliance strategy.
· Should future policy changes occur, the UK government will provide sufficient transition periods in advance.
Regulated separately by the Medicines and Healthcare products Regulatory Agency (MHRA). Status as of July 2026:
· CE marking under old directives (MDD/AIMDD/IVDD): recognised until 30 June 2028
· CE marking under new EU regulations (MDR/IVDR): recognised until 30 June 2030
Important update: MHRA launched a public consultation on 16 February 2026 regarding indefinite recognition of CE marked medical devices; consultation closed on 10 April 2026. MHRA also proposed extending the recognition period for legacy directive devices from 30 June 2028 to 31 December 2028. As of July 2026, consultation results have not yet been published.
Note: Recognition of CE marking does not mean zero compliance obligations. MHRA registration, appointment of a UKRP and UDI implementation remain mandatory local requirements.
· The UK government committed in September 2024 to continue accepting CE marked construction products.
· CE marked construction products may remain on the Great Britain market until 2028.
· Government commitment: If CE recognition is withdrawn in future, at least 2 years’ formal advance notice will be given; no abrupt enforcement changes.
· From 8 January 2026, CE marked products complying with the new EU Construction Products Regulation (EU CPR 2024/3110) are also accepted.
1.Unmanned Aircraft Systems: UK class marking (UK0 UK6) mandatory from 1 January 2026, regulated by the Civil Aviation Authority (CAA).
2.Outdoor Equipment Noise Emissions: New rules effective 13 April 2026, updating noise test methods and removing the requirement to submit declarations of conformity to the Office for Product Safety and Standards (OPSS).
· Minimum height: 5 mm (unless specified otherwise in relevant legislation).
· Proportions: Must scale strictly according to the official template; no stretching or distortion.
· Durability: Must be clear, permanent and indelible.
· Supplementary information: Manufacturer’s name, address and UK Responsible Person (UKRP) details shall be displayed in close proximity to the mark.
Until 31 December 2027: For most product categories, UKCA may be affixed to the product itself, product label, outer packaging or accompanying documentation.
From 1 January 2028: Permanent marking directly onto the product is the general requirement. Exemptions apply for miniature or structurally constrained products.
UKCA vs CE Mark Comparison

Important Clarification: CE certificates issued by EU Notified Bodies cannot be directly converted into UKCA certificates. For sel declaration products, most test evidence and technical files may be reused, but a standalone UK DoC and UKRP appointment are still required.
Applicable to: General household appliances, consumer electronics, simple machinery, non high risk PPE and most consumer goods.
1. Product testing: Perform compliance testing against relevant UK standards (mostly BS standards equivalent to EN standards) at an ISO 17025 accredited laboratory to obtain test reports.
2. Compile technical documentation: Complete Englishlanguage Technical Construction File (TCF), including design drawings, BOM, risk assessment, test reports, user instructions etc.
3. Appoint a UKRP: Mandatory for all manufacturers established outside the United Kingdom.
4. Issue declaration: Sign the UK Declaration of Conformity (UK DoC) by an authorised company signatory.
5. Affix marking: Apply UKCA mark in accordance with rules. Retain technical files and DoC for 10 years for authority inspection.

Applicable to: High risk medical devices, complex PPE, pressure equipment, radio frequency products etc.
1. Complete full scope standard testing at a UKAS accredited laboratory.
2. Submit technical documentation to a UK approved Approved Body (AB) for assessment.
3. Upon successful review, the Approved Body issues a UKCA certificate.
4. Issue UK DoC, appoint UKRP and affix UKCA marking.
5. Undergo periodic surveillance audits by the Approved Body during certificate validity to maintain ongoing compliance.
Launched by the UK government on 1 October 2024 as an optional pathway:
· Manufacturers may use existing EU compliance evidence to apply for UKCA marking.
· Available for both self declaration and third party certification routes.
· Where multiple regulations apply to one product, EU and UK compliance procedures may be combined.
· Precondition: The corresponding EU requirements have been transposed into UK domestic law.