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UKCA marking

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How it works

Five steps from an inquiry to a registered certificate

  1. You send the request

    Product name, HS code and technical data, enough for us to scope the route.

    Your part
  2. We confirm the route

    A specialist confirms the regulations that apply and the document type your product needs.

    Our part
  3. Documents and contract

    You send the supporting documents; we sign a contract with fixed scope and timeline.

    Both sides
  4. Testing and inspection

    Laboratory testing, factory inspection and customs clearance, coordinated by us.

    Our part
  5. You receive the certificate

    Issued, registered, and delivered. We close the project.

    Your part
  • One named specialist One person owns your file from the first email to the registered certificate.
  • Route fixed before testing Scheme, standard and laboratory are settled before a sample is tested, which is where most re-testing starts.
  • Registered documents Certificates and declarations issued by accredited bodies and entered in the official register, where customs can look them up.
  • Measured by the document The engagement ends when the certificate is issued and registered, whatever the hours took.
The short answer

Where CE still works in Great Britain

UKCA marking is the conformity marking for Great Britain, and technically it is almost identical to CE marking. UKCA marking is the conformity marking for Great Britain, created by the Product Safety and Metrology etc. (Amendment etc.) (EU Exit) Regulations 2019 and technically almost identical to CE marking: the same assessment logic, the same standards in most cases, a different declaration and a different mark. In August 2023 the government extended recognition of CE marking indefinitely for most goods regulated by the Department for Business and Trade, so for a large share of products UKCA is optional. Medical devices, construction products and a few other categories follow their own timetables, and those are the ones to check.

  • Created by the 2019 Regulations The Product Safety and Metrology etc. (Amendment etc.) (EU Exit) Regulations 2019 created the mark.
  • Same logic, different paperwork The same assessment logic and, in most cases, the same standards as CE, with a different declaration and a different mark.
  • CE recognised indefinitely In August 2023 the government extended recognition of CE marking indefinitely for most goods regulated by the Department for Business and Trade, so for a large share of products UKCA is optional.
  • The categories to check Medical devices, construction products and a few other categories follow their own timetables. Those are the ones to check.
  • Two UK markets

    UKCA applies in England, Scotland and Wales. Northern Ireland follows EU rules under the Windsor Framework and uses CE, with UKNI beside it where a UK body assessed.

    For goods sold in both, use CE and add UKCA where recognition was not extended.

  • CE recognised indefinitely

    The Product Safety and Metrology (Amendment) Regulations 2024 recognise CE for DBT-regulated goods, among them electrical equipment, EMC, radio, machinery and toys. Medical devices and construction products follow their own timetables.

    Check the regulator's current position before skipping UKCA for those categories.

  • A UK responsible person

    A manufacturer outside the UK needs a UK importer or authorised representative, named in the documentation, who can produce the declaration and technical file for UK market surveillance.

    An EU authorised representative has no standing in Great Britain.

Already started elsewhere

Moving from CE to UKCA, and the project has stalled?

A plan that treats "the UK" as one destination eventually ships the wrong mark to one half of it. Files also go wrong when the EU authorised representative is assumed to cover Great Britain, or when UKCA is skipped for a medical device or construction product without checking that regulator's timetable. Connected consumer devices add a divergence: Great Britain applies the PSTI product security regime, which asks for different documents from the RED cybersecurity rules.

Your CE test reports carry over. The UK regulations keep the essential requirements of the directives they came from, so the same accredited evidence supports the UK declaration. The EU declaration itself cannot be reused, and neither can a Notified Body certificate: where UKCA needs third-party assessment, a UK approved body is a different legal entity and issues its own certificate. The UK importer or authorised representative is a separate appointment from the EU one.

What we handle

  • Gap analysis
  • Testing
  • UK DoC
  • UK responsible person

What to send us

Everything here is something to find before the project starts. The first reply says which of it can go into the file as it is.

  • Your CE technical file, if you have one, and the test reports inside it
  • Where the product ships: Great Britain, Northern Ireland or both
  • Any Notified Body certificate, and whether a UK approved body was approached
  • The name of your UK importer or authorised representative, if one exists

We’ll call you back within an hour.

We will call you back

We respect your time and your privacy. Your details are used to answer this inquiry and nothing else.

  • 2010 Year of foundation
  • 1300+ Certification projects
  • 40+ Countries served
  • 15+ Types of certificates

Great Britain and Northern Ireland are different markets

UKCA applies to Great Britain: England, Scotland and Wales. Northern Ireland continues to follow EU rules under the Windsor Framework, uses CE marking, and has the UKNI mark for cases where a UK body carried out the assessment.

A manufacturer treating "the UK" as one destination will eventually ship the wrong mark to one half of it. Where a product goes to both, the working answer is CE for everything, with UKCA added only for a category where Great Britain has not extended CE recognition.

Which products still need UKCA?

Fewer than the 2021 announcements suggested. In August 2023 the Department for Business and Trade announced that CE marking would be recognised indefinitely for the product regulations it owns, and the Product Safety and Metrology (Amendment) Regulations 2024 wrote that into law. The list covers toys, electrical equipment under the Electrical Equipment (Safety) Regulations 2016, electromagnetic compatibility, radio equipment, machinery, pressure equipment, simple pressure vessels, equipment for explosive atmospheres, personal protective equipment, gas appliances, lifts, measuring and weighing instruments, RoHS, aerosols, outdoor noise, recreational craft and pyrotechnics. For those categories a valid CE marking can still be placed on the Great Britain market.

Outside that list each regulator sets its own timetable. Medical devices sit with the MHRA under the Medical Devices Regulations 2002 and have their own transition dates. Construction products under the retained Construction Products Regulation belong to a different department and are being reformed separately. Marine equipment and several transport-regulated categories are outside the DBT list as well. For any of those, check the regulator's current position before deciding to skip UKCA.

What changes from CE?

Less than the paperwork suggests, and there is no UKCA certification as such: like CE, it is a declaration you sign, with a UK approved body involved only where the regulation names third-party assessment. The 2019 Regulations amended the domestic regulations that had transposed the EU directives, among them the Electrical Equipment (Safety) Regulations 2016, the Electromagnetic Compatibility Regulations 2016, the Radio Equipment Regulations 2017 and the Supply of Machinery (Safety) Regulations 2008, and left the essential requirements untouched. The same test evidence supports both. What differs is the legal furniture: a UK Declaration of Conformity instead of an EU one, UK approved bodies instead of notified bodies, and designated standards instead of harmonised standards.

The two sets of standards have not diverged much so far, but they are separate lists maintained separately, and the Product Regulation and Metrology Act 2025 gives ministers the power to follow or depart from EU rules by regulation. One divergence already exists. Connected consumer devices in Great Britain fall under the Product Security and Telecommunications Infrastructure regime, in force since 29 April 2024, while the EU applies the RED cybersecurity delegated regulation from 1 August 2025; the two ask for different documents. Record which designated standard edition you applied, with its date.

The responsible person requirement

A manufacturer outside the United Kingdom needs an importer or authorised representative established in the UK, named in the documentation and able to produce the declaration and technical file on request. This mirrors the EU arrangement and, like it, is a legal appointment that carries duties toward the Office for Product Safety and Standards and local Trading Standards.

An EU-based authorised representative does not cover Great Britain. The two appointments are separate.

CE and UKCA side by side

European UnionGreat Britain
Legal basisNew Approach directives and regulationsProduct Safety and Metrology etc. (Amendment etc.) (EU Exit) Regulations 2019, as amended
MarkCEUKCA
DeclarationEU Declaration of ConformityUK Declaration of Conformity
Third partyNotified BodyUK approved body
StandardsHarmonised standardsUK designated standards
Local operatorEU importer or authorised representativeUK importer or authorised representative
CE recognised?YesIndefinitely for DBT-regulated goods under the 2024 Regulations; own timetable for medical devices and construction products
Connected-device securityRED Delegated Regulation (EU) 2022/30, from 1 August 2025PSTI product security regime, from 29 April 2024
Northern IrelandCE appliesCE, or UKNI where a UK body assessed

Recognition of CE marking in Great Britain is set per product regulation. Confirm the position for your category before deciding to skip UKCA, and go to the regulator itself when the product is a medical device or a construction product.

Frequently asked questions

Is UKCA marking mandatory?

It depends on the product category. The Product Safety and Metrology (Amendment) Regulations 2024 recognise CE marking indefinitely for most goods regulated by the Department for Business and Trade, which makes UKCA optional for those. Medical devices under the MHRA and construction products under the Construction Products Regulation follow their own timetables, as do marine equipment and several transport categories. The answer is per category and has changed several times, so confirm it against the current regulation.

Can I use my CE test reports for UKCA?

Almost always. The UK regulations carry the same essential requirements as the EU directives they came from, so the same accredited test evidence supports both declarations. What you cannot reuse is the declaration itself or a Notified Body certificate; where third-party assessment is required for UKCA, a UK approved body is a different legal entity and issues its own certificate.

Does UKCA cover Northern Ireland?

No. Northern Ireland follows EU rules under the Windsor Framework and uses CE marking. The UKNI mark exists for the case where a UK body carried out third-party assessment for goods placed on the Northern Ireland market, and it always sits next to the CE mark.

Do I need a UK representative if I already have an EU one?

Yes. The two appointments are separate and an EU authorised representative has no standing in Great Britain. A manufacturer outside the UK needs a UK importer or authorised representative named in the documentation who can produce the declaration and technical file for UK market surveillance.

Keep reading

On the European and British markets

Tell us what you are exporting

Send the product name, HS code and technical data. You get back the applicable route, the document list and a timeline, before any commitment.